| geneid | 256987 |
|---|---|
| ensemblid | ENSG00000164300.17 |
| hgncid | 18825 |
| symbol | SERINC5 |
| name | serine incorporator 5 |
| refseq_nuc | NM_001174072.3 |
| refseq_prot | NP_001167543.1 |
| ensembl_nuc | ENST00000507668.7 |
| ensembl_prot | ENSP00000426237.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 80138727 |
| end | 80256048 |
| strand | - |
| ver | v1.2 |
| region | chr5:80138727-80256048 |
| region5000 | chr5:80133727-80261048 |
| regionname0 | SERINC5_chr5_80138727_80256048 |
| regionname5000 | SERINC5_chr5_80133727_80261048 |
| 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 | 461 | 277 | 83 | 63 | 83 | 16 | 30 | 55 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0002 | 0/0 | 461 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0003 | 0/0 | 461 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0004 | 0/0 | 461 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| 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 | 1386 | 209 | 76 | 51 | 48 | 11 | 21 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| c0002 | 0/0 | 1386 | 64 | 4 | 12 | 35 | 5 | 8 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| c0003 | 0/0 | 1386 | 3 | 1 | 2 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| c0004 | 0/0 | 1386 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| c0005 | 0/0 | 1386 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| c0006 | 0/0 | 1386 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| c0007 | 0/0 | 1386 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| c0008 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| c0009 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| c0010 | 0/0 | 1386 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 5062 | 43 | 9 | 4 | 26 | 0 | 4 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0002 | 0/0 | 5063 | 43 | 7 | 18 | 12 | 1 | 5 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0003 | 0/0 | 5064 | 34 | 0 | 4 | 24 | 4 | 2 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0004 | 0/1 | 5073 | 21 | 2 | 9 | 5 | 2 | 2 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0005 | 0/0 | 5065 | 14 | 2 | 3 | 6 | 0 | 3 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0006 | 0/0 | 5063 | 10 | 3 | 4 | 0 | 3 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0007 | 0/0 | 5064 | 8 | 5 | 2 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0008 | 0/0 | 5067 | 7 | 6 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0009 | 0/0 | 5064 | 5 | 4 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0010 | 0/0 | 5064 | 4 | 4 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0011 | 0/0 | 5074 | 4 | 0 | 4 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0012 | 0/0 | 5077 | 4 | 0 | 3 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0013 | 0/0 | 5053 | 3 | 3 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0014 | 0/0 | 5062 | 3 | 0 | 0 | 3 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0015 | 0/0 | 5081 | 3 | 3 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0016 | 0/0 | 5066 | 3 | 1 | 0 | 2 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0017 | 0/0 | 5060 | 3 | 0 | 3 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0018 | 0/0 | 5060 | 2 | 0 | 2 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0019 | 0/0 | 5066 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0020 | 0/0 | 5072 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0021 | 0/0 | 5048 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0022 | 0/0 | 5062 | 2 | 1 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0023 | 0/0 | 5063 | 2 | 0 | 0 | 0 | 0 | 2 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0024 | 0/0 | 5072 | 2 | 0 | 1 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0025 | 0/0 | 5069 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0026 | 0/0 | 5063 | 2 | 0 | 1 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0027 | 0/0 | 5065 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0028 | 0/0 | 5063 | 2 | 0 | 0 | 0 | 0 | 2 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0029 | 0/0 | 5075 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0030 | 0/0 | 5074 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0031 | 0/0 | 5064 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0032 | 0/0 | 5062 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0033 | 0/0 | 5070 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0034 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0035 | 0/0 | 5045 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0036 | 0/0 | 5066 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0037 | 0/0 | 5067 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0038 | 0/0 | 5065 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0039 | 0/0 | 5066 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0040 | 0/0 | 5075 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0041 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0042 | 0/0 | 5076 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0043 | 0/0 | 5053 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0044 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0045 | 0/0 | 5067 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0046 | 0/0 | 5072 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0047 | 0/0 | 5070 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0048 | 0/0 | 5065 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0049 | 0/0 | 5069 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0050 | 0/0 | 5065 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0051 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0052 | 0/0 | 5065 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0053 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0054 | 0/0 | 5082 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0055 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0056 | 0/0 | 5062 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0057 | 0/0 | 5062 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0058 | 0/0 | 5063 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0059 | 0/0 | 5082 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0060 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0061 | 0/0 | 5062 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0062 | 0/0 | 5066 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0063 | 0/0 | 5060 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0064 | 0/0 | 5062 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0065 | 0/0 | 5062 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0066 | 0/0 | 5061 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0067 | 0/0 | 5064 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0068 | 0/0 | 5060 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0069 | 0/0 | 5061 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0070 | 0/0 | 5061 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0071 | 0/0 | 5067 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0072 | 0/0 | 5068 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0073 | 0/0 | 5065 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0074 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0075 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0076 | 0/0 | 5062 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0077 | 0/0 | 5064 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| t0078 | 1/0 | 5063 | 1 | 0 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| 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 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0074 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0233 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| 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 | 1386 | 209 | 76 | 51 | 48 | 11 | 21 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0002 | 0/0 | 1386 | 64 | 4 | 12 | 35 | 5 | 8 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0006 | 0/0 | 1386 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0009 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0010 | 0/0 | 1386 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0002c0003 | 0/0 | 1386 | 3 | 1 | 2 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0002c0004 | 0/0 | 1386 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0002c0005 | 0/0 | 1386 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0003c0007 | 0/0 | 1386 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0004c0008 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6447 | 42 | 9 | 4 | 25 | 0 | 4 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0002 | 0/0 | 6448 | 42 | 7 | 17 | 12 | 1 | 5 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0004 | 0/1 | 6458 | 20 | 2 | 8 | 5 | 2 | 2 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0006 | 0/0 | 6448 | 10 | 3 | 4 | 0 | 3 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0007 | 0/0 | 6449 | 8 | 5 | 2 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0008 | 0/0 | 6452 | 7 | 6 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0009 | 0/0 | 6449 | 4 | 3 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0010 | 0/0 | 6449 | 4 | 4 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0011 | 0/0 | 6459 | 3 | 0 | 3 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0012 | 0/0 | 6462 | 4 | 0 | 3 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0013 | 0/0 | 6438 | 3 | 3 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0014 | 0/0 | 6447 | 3 | 0 | 0 | 3 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0015 | 0/0 | 6466 | 3 | 3 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0018 | 0/0 | 6445 | 2 | 0 | 2 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0020 | 0/0 | 6457 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0021 | 0/0 | 6433 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0022 | 0/0 | 6447 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0023 | 0/0 | 6448 | 2 | 0 | 0 | 0 | 0 | 2 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0024 | 0/0 | 6457 | 2 | 0 | 1 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0025 | 0/0 | 6454 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0026 | 0/0 | 6448 | 2 | 0 | 1 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0028 | 0/0 | 6448 | 2 | 0 | 0 | 0 | 0 | 2 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0029 | 0/0 | 6460 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0030 | 0/0 | 6459 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0032 | 0/0 | 6447 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0033 | 0/0 | 6455 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0034 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0036 | 0/0 | 6451 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0037 | 0/0 | 6452 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0038 | 0/0 | 6450 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0039 | 0/0 | 6451 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0040 | 0/0 | 6460 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0041 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0042 | 0/0 | 6461 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0043 | 0/0 | 6438 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0044 | 0/0 | 6437 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0046 | 0/0 | 6457 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0047 | 0/0 | 6455 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0048 | 0/0 | 6450 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0049 | 0/0 | 6454 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0050 | 0/0 | 6450 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0051 | 0/0 | 6449 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0052 | 0/0 | 6450 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0053 | 0/0 | 6466 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0054 | 0/0 | 6467 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0055 | 0/0 | 6464 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0056 | 0/0 | 6447 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0057 | 0/0 | 6447 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0058 | 0/0 | 6448 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0059 | 0/0 | 6467 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0060 | 0/0 | 6437 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0061 | 0/0 | 6447 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0062 | 0/0 | 6451 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0063 | 0/0 | 6445 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0064 | 0/0 | 6447 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0065 | 0/0 | 6447 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0066 | 0/0 | 6446 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0075 | 0/0 | 6449 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0076 | 0/0 | 6447 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0001t0078 | 1/0 | 6448 | 1 | 0 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0002t0003 | 0/0 | 6449 | 34 | 0 | 4 | 24 | 4 | 2 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0002t0005 | 0/0 | 6450 | 12 | 1 | 3 | 6 | 0 | 2 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0002t0016 | 0/0 | 6451 | 2 | 0 | 0 | 2 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0002t0017 | 0/0 | 6445 | 3 | 0 | 3 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0002t0022 | 0/0 | 6447 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0002t0027 | 0/0 | 6450 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0002t0031 | 0/0 | 6449 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0002t0067 | 0/0 | 6449 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0002t0068 | 0/0 | 6445 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0002t0069 | 0/0 | 6446 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0002t0070 | 0/0 | 6446 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0002t0071 | 0/0 | 6452 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0002t0072 | 0/0 | 6453 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0002t0073 | 0/0 | 6450 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0002t0074 | 0/0 | 6449 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0002t0077 | 0/0 | 6449 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0006t0020 | 0/0 | 6457 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0006t0045 | 0/0 | 6452 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0009t0035 | 0/0 | 6430 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0001c0010t0005 | 0/0 | 6450 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0002c0003t0004 | 0/0 | 6458 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0002c0003t0009 | 0/0 | 6449 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0002c0003t0011 | 0/0 | 6459 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0002c0004t0005 | 0/0 | 6450 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0002c0004t0016 | 0/0 | 6451 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0002c0005t0019 | 0/0 | 6451 | 2 | 2 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0003c0007t0002 | 0/0 | 6448 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| a0004c0008t0001 | 0/0 | 6447 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | copy fasta | chr5 | 80133727 | 80261048 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0233 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0006g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0006g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0007g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0007g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0007g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0008g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0008g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0008g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0008g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0008g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0009g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0009g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0009g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0010g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0010g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0010g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0011g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0011g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0011g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0012g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0012g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0012g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0012g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0013g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0013g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0013g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0014g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0014g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0014g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0015g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0015g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0015g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0018g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0018g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0020g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0021g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0021g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0022g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0023g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0023g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0024g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0024g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0025g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0025g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0026g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0026g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0028g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0028g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0029g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0029g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0030g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0030g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0032g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0033g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0034g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0036g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0037g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0038g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0039g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0040g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0041g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0042g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0043g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0044g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0046g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0047g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0048g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0049g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0050g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0051g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0052g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0053g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0054g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0055g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0056g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0057g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0058g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0059g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0060g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0061g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0062g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0063g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0064g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0065g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0066g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0075g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0076g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0001t0078g0074 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0005g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0005g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0005g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0016g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0016g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0017g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0017g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0017g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0022g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0027g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0027g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0031g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0067g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0068g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0069g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0070g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0071g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0072g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0073g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0074g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0002t0077g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0006t0020g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0006t0045g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0009t0035g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0001c0010t0005g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0002c0003t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0002c0003t0009g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0002c0003t0011g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0002c0004t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0002c0004t0016g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0002c0005t0019g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0002c0005t0019g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0003c0007t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| a0004c0008t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0120 | EUR | GBR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0023 | EUR | GBR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00140 | hp1 | a0001 | c0001 | t0007 | g0249 | EUR | GBR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00140 | hp2 | a0001 | c0001 | t0026 | g0244 | EUR | GBR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0193 | EUR | FIN | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00323 | hp2 | a0001 | c0001 | t0022 | g0185 | EUR | FIN | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00408 | hp2 | a0001 | c0002 | t0003 | g0090 | EAS | CHS | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00438 | hp1 | a0001 | c0002 | t0003 | g0085 | EAS | CHS | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0087 | EAS | CHS | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00609 | hp2 | a0001 | c0002 | t0069 | g0246 | EAS | CHS | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00621 | hp1 | a0001 | c0002 | t0005 | g0176 | EAS | CHS | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00639 | hp2 | a0002 | c0003 | t0004 | g0118 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00642 | hp2 | a0001 | c0002 | t0067 | g0250 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00733 | hp2 | a0001 | c0001 | t0006 | g0179 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0175 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00735 | hp2 | a0001 | c0001 | t0065 | g0132 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0114 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG00741 | hp2 | a0003 | c0007 | t0002 | g0124 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0154 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01070 | hp1 | a0001 | c0002 | t0073 | g0204 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0203 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01106 | hp1 | a0001 | c0001 | t0011 | g0245 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01106 | hp2 | a0002 | c0003 | t0011 | g0119 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0142 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01167 | hp2 | a0001 | c0001 | t0047 | g0261 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01168 | hp2 | a0001 | c0001 | t0018 | g0002 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01169 | hp2 | a0001 | c0001 | t0018 | g0003 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01175 | hp1 | a0001 | c0002 | t0005 | g0137 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0178 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01243 | hp1 | a0001 | c0001 | t0059 | g0059 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0079 | AMR | CLM | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01255 | hp2 | a0001 | c0001 | t0012 | g0180 | AMR | CLM | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01256 | hp1 | a0001 | c0001 | t0012 | g0251 | AMR | CLM | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01261 | hp1 | a0001 | c0001 | t0012 | g0238 | AMR | CLM | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0117 | AMR | CLM | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0199 | AMR | CLM | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01361 | hp2 | a0001 | c0001 | t0007 | g0083 | AMR | CLM | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0048 | AMR | CLM | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01433 | hp2 | a0001 | c0002 | t0017 | g0072 | AMR | CLM | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0267 | AMR | CLM | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0186 | AMR | CLM | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01515 | hp1 | a0001 | c0001 | t0063 | g0164 | EUR | IBS | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01515 | hp2 | a0001 | c0002 | t0003 | g0078 | EUR | IBS | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0167 | EUR | IBS | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0077 | EUR | IBS | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01517 | hp1 | a0001 | c0002 | t0003 | g0081 | EUR | IBS | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0076 | EUR | IBS | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01884 | hp1 | a0001 | c0001 | t0010 | g0235 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01884 | hp2 | a0001 | c0002 | t0027 | g0148 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0241 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01891 | hp2 | a0001 | c0001 | t0015 | g0063 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01934 | hp1 | a0001 | c0001 | t0026 | g0070 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01934 | hp2 | a0001 | c0002 | t0003 | g0080 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01943 | hp1 | a0001 | c0001 | t0024 | g0005 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01943 | hp2 | a0001 | c0001 | t0062 | g0283 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01975 | hp1 | a0001 | c0002 | t0005 | g0263 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0282 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01978 | hp1 | a0001 | c0002 | t0017 | g0075 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02004 | hp2 | a0001 | c0001 | t0011 | g0123 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0247 | EAS | KHV | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0205 | EAS | KHV | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | KHV | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02040 | hp2 | a0001 | c0002 | t0005 | g0038 | EAS | KHV | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0064 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02055 | hp2 | a0001 | c0002 | t0005 | g0058 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02083 | hp1 | a0001 | c0001 | t0056 | g0198 | EAS | KHV | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0229 | EAS | KHV | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0182 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0099 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02148 | hp2 | a0001 | c0002 | t0005 | g0054 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | CDX | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0041 | EAS | CDX | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02257 | hp1 | a0001 | c0001 | t0052 | g0055 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0275 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02258 | hp2 | a0001 | c0001 | t0043 | g0234 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02273 | hp1 | a0001 | c0002 | t0017 | g0145 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0139 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02300 | hp1 | a0001 | c0001 | t0057 | g0196 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02300 | hp2 | a0001 | c0001 | t0011 | g0009 | AMR | PEL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02451 | hp1 | a0001 | c0002 | t0022 | g0272 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02451 | hp2 | a0001 | c0006 | t0020 | g0127 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0108 | EAS | KHV | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | KHV | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02572 | hp2 | a0001 | c0001 | t0054 | g0253 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0125 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02647 | hp1 | a0001 | c0001 | t0048 | g0143 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02647 | hp2 | a0001 | c0001 | t0058 | g0243 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02717 | hp1 | a0001 | c0006 | t0045 | g0128 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0135 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02738 | hp1 | a0001 | c0002 | t0005 | g0161 | SAS | PJL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0052 | SAS | PJL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02818 | hp1 | a0001 | c0001 | t0015 | g0256 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02818 | hp2 | a0001 | c0001 | t0042 | g0065 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02895 | hp1 | a0001 | c0001 | t0013 | g0068 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0281 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0129 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0270 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02922 | hp1 | a0001 | c0001 | t0036 | g0254 | AFR | ESN | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0208 | AFR | ESN | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02965 | hp1 | a0001 | c0001 | t0021 | g0053 | AFR | ESN | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02965 | hp2 | a0002 | c0004 | t0005 | g0110 | AFR | ESN | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02976 | hp1 | a0001 | c0002 | t0027 | g0274 | AFR | ESN | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02976 | hp2 | a0001 | c0001 | t0040 | g0066 | AFR | ESN | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03041 | hp1 | a0001 | c0001 | t0041 | g0279 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03041 | hp2 | a0001 | c0001 | t0029 | g0102 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03098 | hp1 | a0001 | c0001 | t0050 | g0265 | AFR | MSL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03098 | hp2 | a0001 | c0001 | t0029 | g0144 | AFR | MSL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03130 | hp1 | a0001 | c0001 | t0034 | g0207 | AFR | ESN | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0266 | AFR | ESN | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03139 | hp1 | a0002 | c0005 | t0019 | g0273 | AFR | ESN | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03139 | hp2 | a0001 | c0001 | t0061 | g0206 | AFR | ESN | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03195 | hp2 | a0001 | c0001 | t0025 | g0050 | AFR | ESN | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0062 | AFR | MSL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03209 | hp2 | a0001 | c0001 | t0055 | g0276 | AFR | MSL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03225 | hp1 | a0001 | c0001 | t0044 | g0149 | AFR | MSL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0259 | AFR | MSL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03239 | hp1 | a0001 | c0002 | t0077 | g0285 | SAS | PJL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03239 | hp2 | a0001 | c0001 | t0012 | g0131 | SAS | PJL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03453 | hp1 | a0001 | c0001 | t0033 | g0060 | AFR | MSL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03453 | hp2 | a0001 | c0001 | t0020 | g0057 | AFR | MSL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0158 | AFR | MSL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03486 | hp2 | a0001 | c0001 | t0013 | g0140 | AFR | MSL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03490 | hp1 | a0001 | c0001 | t0028 | g0160 | SAS | PJL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0171 | SAS | PJL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03491 | hp1 | a0001 | c0002 | t0003 | g0096 | SAS | PJL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03491 | hp2 | a0001 | c0001 | t0032 | g0004 | SAS | PJL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03492 | hp1 | a0001 | c0002 | t0005 | g0095 | SAS | PJL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03492 | hp2 | a0001 | c0001 | t0028 | g0159 | SAS | PJL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0126 | AFR | ESN | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03516 | hp2 | a0001 | c0001 | t0025 | g0051 | AFR | ESN | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03540 | hp1 | a0001 | c0001 | t0049 | g0242 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03540 | hp2 | a0001 | c0001 | t0075 | g0284 | AFR | GWD | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03579 | hp1 | a0001 | c0001 | t0015 | g0258 | AFR | MSL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03579 | hp2 | a0002 | c0004 | t0016 | g0231 | AFR | MSL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03688 | hp1 | a0001 | c0002 | t0068 | g0188 | SAS | STU | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | STU | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03704 | hp1 | a0001 | c0001 | t0023 | g0130 | SAS | PJL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03834 | hp2 | a0001 | c0001 | t0064 | g0212 | SAS | BEB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | BEB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03927 | hp2 | a0001 | c0001 | t0066 | g0172 | SAS | BEB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG04184 | hp1 | a0001 | c0001 | t0009 | g0226 | SAS | BEB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | BEB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG04199 | hp1 | a0001 | c0010 | t0005 | g0223 | SAS | STU | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG04199 | hp2 | a0001 | c0002 | t0072 | g0210 | SAS | STU | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG04204 | hp1 | a0001 | c0002 | t0070 | g0189 | SAS | STU | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG04204 | hp2 | a0001 | c0001 | t0076 | g0286 | SAS | STU | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18522 | hp2 | a0001 | c0001 | t0053 | g0061 | AFR | YRI | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0026 | EAS | CHB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18747 | hp2 | a0001 | c0002 | t0003 | g0016 | EAS | CHB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18940 | hp1 | a0001 | c0002 | t0003 | g0217 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18942 | hp1 | a0001 | c0002 | t0003 | g0146 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18942 | hp2 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18945 | hp2 | a0001 | c0002 | t0003 | g0082 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18948 | hp1 | a0001 | c0002 | t0003 | g0202 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18952 | hp2 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18954 | hp1 | a0001 | c0001 | t0024 | g0165 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18963 | hp1 | a0001 | c0002 | t0003 | g0036 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18969 | hp1 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18969 | hp2 | a0001 | c0002 | t0003 | g0192 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18971 | hp1 | a0001 | c0002 | t0005 | g0214 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18971 | hp2 | a0001 | c0002 | t0003 | g0035 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18977 | hp1 | a0001 | c0002 | t0003 | g0106 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18983 | hp1 | a0001 | c0002 | t0016 | g0033 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18983 | hp2 | a0004 | c0008 | t0001 | g0008 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18984 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18990 | hp1 | a0001 | c0001 | t0014 | g0086 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18995 | hp2 | a0001 | c0001 | t0014 | g0152 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19003 | hp1 | a0001 | c0002 | t0003 | g0168 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19030 | hp1 | a0001 | c0001 | t0013 | g0067 | AFR | LWK | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19030 | hp2 | a0001 | c0001 | t0039 | g0264 | AFR | LWK | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19043 | hp1 | a0001 | c0001 | t0021 | g0141 | AFR | LWK | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | LWK | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19057 | hp2 | a0001 | c0002 | t0016 | g0034 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19065 | hp1 | a0001 | c0002 | t0074 | g0091 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19074 | hp2 | a0001 | c0002 | t0003 | g0224 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19079 | hp2 | a0001 | c0002 | t0003 | g0147 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19081 | hp2 | a0001 | c0002 | t0003 | g0013 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19082 | hp2 | a0001 | c0002 | t0005 | g0105 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19086 | hp2 | a0001 | c0002 | t0005 | g0201 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19087 | hp1 | a0001 | c0001 | t0060 | g0017 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19087 | hp2 | a0001 | c0002 | t0071 | g0037 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0069 | AFR | YRI | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0240 | AFR | YRI | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA20129 | hp2 | a0001 | c0001 | t0037 | g0262 | AFR | ASW | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA20752 | hp1 | a0001 | c0002 | t0003 | g0184 | EUR | TSI | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA20752 | hp2 | a0001 | c0002 | t0031 | g0001 | EUR | TSI | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA20805 | hp1 | a0001 | c0001 | t0046 | g0260 | EUR | TSI | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0173 | EUR | TSI | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA20905 | hp1 | a0001 | c0001 | t0023 | g0220 | SAS | GIH | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0222 | SAS | GIH | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02109 | hp1 | a0001 | c0001 | t0010 | g0183 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0174 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0150 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02486 | hp2 | a0002 | c0003 | t0009 | g0228 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | ACB | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03471 | hp1 | a0001 | c0001 | t0030 | g0257 | AFR | MSL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG03471 | hp2 | a0001 | c0001 | t0051 | g0236 | AFR | MSL | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | USA | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| HG06807 | hp2 | a0001 | c0009 | t0035 | g0209 | AFR | USA | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18955 | hp1 | a0001 | c0002 | t0005 | g0122 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA18955 | hp2 | a0001 | c0001 | t0014 | g0019 | EAS | JPT | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA20300 | hp1 | a0001 | c0001 | t0030 | g0255 | AFR | USA | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | USA | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA21309 | hp1 | a0001 | c0001 | t0038 | g0111 | AFR | LWK | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| NA21309 | hp2 | a0002 | c0005 | t0019 | g0042 | AFR | LWK | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0233 | REF | REF | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0078 | g0074 | REF | REF | SERINC5_chr5_80133727_80261048 | SERINC5 | chr5 | 80133727 | 80261048 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:80143728
|
C | T | 1 | a0004 | 1 | NA18983.hp2 | missense_variant | MODERATE | c.1321G>A | p.Val441Met | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1447/6448 | 1321/1386 | 441/461 | chr5 | 80143728 | ||
| chr5:80175027
|
C | T | 1 | a0003 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.478G>A | p.Val160Ile | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/12 | 604/6448 | 478/1386 | 160/461 | chr5 | 80175027 | ||
| chr5:80177961
|
C | G | 1 | a0002 | 7 | HG00639.hp2 HG01106.hp2 HG02486.hp2 others(4): Show |
missense_variant | MODERATE | c.299G>C | p.Cys100Ser | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 3/12 | 425/6448 | 299/1386 | 100/461 | chr5 | 80177961 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:80143807
|
G | A | 3 | a0001c0002a0001c0010a0002c0004 | 67 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(64): Show |
synonymous_variant | LOW | c.1242C>T | p.Tyr414Tyr | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1368/6448 | 1242/1386 | 414/461 | chr5 | 80143807 | ||
| chr5:80146107
|
G | A | 2 | a0001c0009a0002c0005 | 3 | HG03139.hp1 HG06807.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.1221C>T | p.Thr407Thr | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/12 | 1347/6448 | 1221/1386 | 407/461 | chr5 | 80146107 | ||
| chr5:80169461
|
A | G | 1 | a0001c0006 | 2 | HG02451.hp2 HG02717.hp1 |
synonymous_variant | LOW | c.637T>C | p.Leu213Leu | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/12 | 763/6448 | 637/1386 | 213/461 | chr5 | 80169461 | ||
| chr5:80175028
|
G | A | 1 | a0001c0010 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.477C>T | p.Ala159Ala | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/12 | 603/6448 | 477/1386 | 159/461 | chr5 | 80175028 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:80138929
|
C | T | 1 | a0001c0001t0065 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4734G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4734 | chr5 | 80138929 | |||||
| chr5:80139058
|
G | A | 1 | a0001c0002t0067 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4605C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4605 | chr5 | 80139058 | |||||
| chr5:80139492
|
T | C | 1 | a0001c0001t0030 | 2 | HG03471.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4171A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4171 | chr5 | 80139492 | |||||
| chr5:80139594
|
A | AGAGAGAG others(20): Show |
2 | a0001c0001t0033a0001c0001t0047 | 2 | HG01167.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4068_*4069insCTCT others(23): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4068 | chr5 | 80139594 | |||||
| chr5:80139594
|
A | AGAGAGAG others(22): Show |
1 | a0001c0001t0046 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4068_*4069insCTCT others(25): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4068 | chr5 | 80139594 | |||||
| chr5:80139596
|
A | AAGAG | 28 | a0001c0001t0006a0001c0001t0009a0001c0001t0022others(25): Show | 90 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*4063_*4066dupCTCT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4066 | chr5 | 80139596 | |||||
| chr5:80139596
|
A | AAGAGAGA others(3): Show |
1 | a0001c0001t0025 | 2 | HG03195.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4057_*4066dupCTCT others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4066 | chr5 | 80139596 | |||||
| chr5:80139596
|
A | AAGAGAGA others(5): Show |
1 | a0001c0001t0021 | 2 | HG02965.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4055_*4066dupCTCT others(8): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4066 | chr5 | 80139596 | |||||
| chr5:80139596
|
A | AAGAGAGA others(7): Show |
7 | a0001c0001t0004a0001c0001t0011a0001c0001t0012others(4): Show | 32 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*4053_*4066dupCTCT others(10): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4066 | chr5 | 80139596 | |||||
| chr5:80139596
|
A | AAGAGAGA others(9): Show |
4 | a0001c0001t0013a0001c0001t0043a0001c0001t0044others(1): Show | 6 | HG02258.hp2 HG02895.hp1 HG03209.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4066_*4067insCTCT others(12): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4066 | chr5 | 80139596 | |||||
| chr5:80139596
|
A | AAGAGAGA others(11): Show |
1 | a0001c0001t0029 | 2 | HG03041.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4066_*4067insCTCT others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4066 | chr5 | 80139596 | |||||
| chr5:80139596
|
A | AAGAGAGA others(13): Show |
6 | a0001c0001t0010a0001c0001t0015a0001c0001t0050others(3): Show | 11 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4066_*4067insCTCT others(16): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4066 | chr5 | 80139596 | |||||
| chr5:80139596
|
A | AAGAGAGA others(15): Show |
3 | a0001c0001t0038a0001c0001t0039a0002c0005t0019 | 4 | HG03139.hp1 NA19030.hp2 NA21309.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4066_*4067insCTCT others(18): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4066 | chr5 | 80139596 | |||||
| chr5:80139596
|
A | AAGAGAGA others(17): Show |
4 | a0001c0001t0008a0001c0001t0036a0001c0001t0037others(1): Show | 10 | HG01496.hp1 HG01891.hp1 HG02145.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4066_*4067insCTCT others(20): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4066 | chr5 | 80139596 | |||||
| chr5:80139596
|
A | AAGAGAGA others(19): Show |
4 | a0001c0001t0020a0001c0001t0041a0001c0001t0049others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4066_*4067insCTCT others(22): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4066 | chr5 | 80139596 | |||||
| chr5:80139596
|
A | AAGAGAGA others(21): Show |
2 | a0001c0001t0040a0001c0001t0042 | 2 | HG02818.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4066_*4067insCTCT others(24): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4066 | chr5 | 80139596 | |||||
| chr5:80139596
|
A | G | 4 | a0001c0001t0033a0001c0001t0046a0001c0001t0047others(1): Show | 4 | HG00609.hp2 HG01167.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4067T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4067 | chr5 | 80139596 | |||||
| chr5:80139606
|
G | GAGAGAGA others(5): Show |
1 | a0001c0001t0030 | 2 | HG03471.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4056_*4057insATCT others(8): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 4056 | chr5 | 80139606 | |||||
| chr5:80139695
|
A | G | 5 | a0001c0001t0020a0001c0001t0040a0001c0001t0041others(2): Show | 5 | HG02451.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3968T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 3968 | chr5 | 80139695 | |||||
| chr5:80139860
|
C | T | 19 | a0001c0001t0062a0001c0002t0003a0001c0002t0005others(16): Show | 67 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*3803G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 3803 | chr5 | 80139860 | |||||
| chr5:80139939
|
A | G | 1 | a0001c0001t0061 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3724T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 3724 | chr5 | 80139939 | |||||
| chr5:80139980
|
G | A | 12 | a0001c0001t0006a0001c0001t0009a0001c0001t0022others(9): Show | 26 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3683C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 3683 | chr5 | 80139980 | |||||
| chr5:80140086
|
T | C | 2 | a0001c0009t0035a0002c0005t0019 | 3 | HG03139.hp1 HG06807.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3577A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 3577 | chr5 | 80140086 | |||||
| chr5:80140100
|
C | T | 1 | a0001c0001t0023 | 2 | HG03704.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3563G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 3563 | chr5 | 80140100 | |||||
| chr5:80140174
|
C | T | 1 | a0001c0001t0058 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3489G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 3489 | chr5 | 80140174 | |||||
| chr5:80140305
|
C | CA | 2 | a0001c0001t0007a0001c0001t0042 | 9 | HG00140.hp1 HG01109.hp1 HG01361.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3357dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 3357 | chr5 | 80140305 | |||||
| chr5:80140305
|
CA | C | 18 | a0001c0001t0001a0001c0001t0014a0001c0001t0018others(15): Show | 62 | HG00438.hp2 HG00735.hp2 HG01074.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*3357delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 3357 | chr5 | 80140305 | |||||
| chr5:80140305
|
CAA | C | 8 | a0001c0001t0015a0001c0001t0048a0001c0001t0050others(5): Show | 11 | HG01891.hp2 HG02257.hp1 HG02647.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3356_*3357delTT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 3356 | chr5 | 80140305 | |||||
| chr5:80140305
|
CAAA | C | 17 | a0001c0001t0009a0001c0001t0010a0001c0001t0011others(14): Show | 38 | HG00609.hp2 HG00621.hp1 HG01070.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*3355_*3357delTTT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 3355 | chr5 | 80140305 | |||||
| chr5:80140305
|
CAAAA | C | 23 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(20): Show | 95 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*3354_*3357delTTTT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 3354 | chr5 | 80140305 | |||||
| chr5:80140305
|
CAAAAA | C | 5 | a0001c0001t0022a0001c0001t0024a0001c0001t0029others(2): Show | 7 | HG00323.hp2 HG01943.hp1 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3353_*3357delTTTT others(1): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 3353 | chr5 | 80140305 | |||||
| chr5:80140305
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0013a0001c0001t0043 | 4 | HG02258.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3348_*3357delTTTT others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 3348 | chr5 | 80140305 | |||||
| chr5:80140305
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0021a0001c0001t0044a0001c0001t0060 | 4 | HG02965.hp1 HG03225.hp1 NA19043.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3347_*3357delTTTT others(7): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 3347 | chr5 | 80140305 | |||||
| chr5:80140363
|
A | G | 70 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(67): Show | 175 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*3300T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 3300 | chr5 | 80140363 | |||||
| chr5:80140636
|
G | A | 8 | a0001c0001t0004a0001c0001t0011a0001c0001t0012others(5): Show | 34 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*3027C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 3027 | chr5 | 80140636 | |||||
| chr5:80140698
|
C | T | 1 | a0001c0001t0043 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2965G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 2965 | chr5 | 80140698 | |||||
| chr5:80141063
|
G | A | 1 | a0001c0002t0073 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2600C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 2600 | chr5 | 80141063 | |||||
| chr5:80141330
|
G | A | 1 | a0001c0001t0055 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2333C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 2333 | chr5 | 80141330 | |||||
| chr5:80141346
|
C | T | 1 | a0001c0001t0014 | 3 | NA18955.hp2 NA18990.hp1 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2317G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 2317 | chr5 | 80141346 | |||||
| chr5:80141460
|
G | C | 5 | a0001c0001t0013a0001c0001t0021a0001c0001t0043others(2): Show | 8 | HG02258.hp2 HG02717.hp1 HG02895.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2203C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 2203 | chr5 | 80141460 | |||||
| chr5:80141463
|
AGTTTCTC others(9): Show |
A | 23 | a0001c0001t0008a0001c0001t0010a0001c0001t0013others(20): Show | 36 | HG01167.hp2 HG01496.hp1 HG01884.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2184_*2199delGTGT others(12): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 2184 | chr5 | 80141463 | |||||
| chr5:80141506
|
G | A | 65 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(62): Show | 168 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*2157C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 2157 | chr5 | 80141506 | |||||
| chr5:80141616
|
C | T | 11 | a0001c0001t0004a0001c0001t0011a0001c0001t0012others(8): Show | 39 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*2047G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 2047 | chr5 | 80141616 | |||||
| chr5:80141751
|
G | A | 2 | a0001c0001t0051a0001c0001t0052 | 2 | HG02257.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1912C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1912 | chr5 | 80141751 | |||||
| chr5:80141765
|
CTT | C | 2 | a0001c0001t0018a0001c0001t0063 | 3 | HG01168.hp2 HG01169.hp2 HG01515.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1896_*1897delAA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1896 | chr5 | 80141765 | |||||
| chr5:80141798
|
A | C | 66 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(63): Show | 169 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*1865T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1865 | chr5 | 80141798 | |||||
| chr5:80141924
|
AATTT | A | 1 | a0001c0002t0017 | 3 | HG01433.hp2 HG01978.hp1 HG02273.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1735_*1738delAAAT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1735 | chr5 | 80141924 | |||||
| chr5:80141995
|
C | T | 1 | a0001c0001t0076 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1668G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1668 | chr5 | 80141995 | |||||
| chr5:80142036
|
C | T | 3 | a0001c0001t0033a0001c0001t0046a0001c0001t0047 | 3 | HG01167.hp2 HG03453.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1627G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1627 | chr5 | 80142036 | |||||
| chr5:80142081
|
T | C | 5 | a0001c0001t0020a0001c0001t0040a0001c0001t0041others(2): Show | 5 | HG02451.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1582A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1582 | chr5 | 80142081 | |||||
| chr5:80142238
|
G | GA | 19 | a0001c0001t0066a0001c0002t0003a0001c0002t0005others(16): Show | 67 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1424dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1424 | chr5 | 80142238 | |||||
| chr5:80142310
|
T | G | 1 | a0001c0002t0031 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1353A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1353 | chr5 | 80142310 | |||||
| chr5:80142356
|
T | C | 87 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(84): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*1307A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1307 | chr5 | 80142356 | |||||
| chr5:80142414
|
A | G | 65 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(62): Show | 168 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*1249T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1249 | chr5 | 80142414 | |||||
| chr5:80142431
|
C | T | 5 | a0001c0001t0013a0001c0001t0021a0001c0001t0043others(2): Show | 8 | HG02258.hp2 HG02717.hp1 HG02895.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1232G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1232 | chr5 | 80142431 | |||||
| chr5:80142454
|
C | G | 65 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(62): Show | 168 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*1209G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1209 | chr5 | 80142454 | |||||
| chr5:80142488
|
C | T | 1 | a0001c0001t0065 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1175G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1175 | chr5 | 80142488 | |||||
| chr5:80142489
|
G | C | 65 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(62): Show | 168 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*1174C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1174 | chr5 | 80142489 | |||||
| chr5:80142511
|
G | A | 1 | a0001c0002t0027 | 2 | HG01884.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1152C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1152 | chr5 | 80142511 | |||||
| chr5:80142594
|
C | T | 65 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(62): Show | 168 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*1069G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1069 | chr5 | 80142594 | |||||
| chr5:80142625
|
C | T | 1 | a0001c0001t0057 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1038G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 1038 | chr5 | 80142625 | |||||
| chr5:80142665
|
C | T | 11 | a0001c0001t0020a0001c0001t0036a0001c0001t0037others(8): Show | 12 | HG02451.hp2 HG02818.hp2 HG02922.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*998G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 998 | chr5 | 80142665 | |||||
| chr5:80142882
|
A | C | 12 | a0001c0001t0004a0001c0001t0011a0001c0001t0012others(9): Show | 40 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*781T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 781 | chr5 | 80142882 | |||||
| chr5:80143063
|
T | C | 3 | a0001c0001t0026a0001c0001t0064a0001c0001t0076 | 4 | HG00140.hp2 HG01934.hp1 HG03834.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*600A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 600 | chr5 | 80143063 | |||||
| chr5:80143103
|
G | A | 54 | a0001c0001t0006a0001c0001t0008a0001c0001t0009others(51): Show | 129 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*560C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 560 | chr5 | 80143103 | |||||
| chr5:80143262
|
C | G | 2 | a0001c0001t0029a0001c0001t0030 | 4 | HG03041.hp2 HG03098.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*401G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 401 | chr5 | 80143262 | |||||
| chr5:80143324
|
A | G | 57 | a0001c0001t0006a0001c0001t0008a0001c0001t0009others(54): Show | 132 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*339T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 339 | chr5 | 80143324 | |||||
| chr5:80143383
|
T | C | 1 | a0001c0001t0065 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*280A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 280 | chr5 | 80143383 | |||||
| chr5:80143387
|
G | T | 1 | a0001c0001t0033 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*276C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 276 | chr5 | 80143387 | |||||
| chr5:80143445
|
C | T | 2 | a0001c0001t0029a0001c0001t0030 | 4 | HG03041.hp2 HG03098.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*218G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 218 | chr5 | 80143445 | |||||
| chr5:80143490
|
T | C | 19 | a0001c0001t0066a0001c0002t0003a0001c0002t0005others(16): Show | 67 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*173A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 173 | chr5 | 80143490 | |||||
| chr5:80143537
|
T | C | 1 | a0001c0001t0028 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*126A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 126 | chr5 | 80143537 | |||||
| chr5:80143538
|
TC | T | 2 | a0001c0001t0029a0001c0001t0030 | 4 | HG03041.hp2 HG03098.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*124delG | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 124 | chr5 | 80143538 | |||||
| chr5:80143553
|
T | C | 1 | a0001c0002t0074 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*110A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 110 | chr5 | 80143553 | |||||
| chr5:80143578
|
G | A | 2 | a0001c0001t0029a0001c0001t0030 | 4 | HG03041.hp2 HG03098.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*85C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 12/12 | 85 | chr5 | 80143578 | |||||
| chr5:80255937
|
C | G | 1 | a0001c0001t0032 | 1 | HG03491.hp2 | 5_prime_UTR_variant | MODIFIER | c.-15G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/12 | 15 | chr5 | 80255937 | |||||
| chr5:80255939
|
G | A | 1 | a0001c0001t0075 | 1 | HG03540.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-17C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/12 | chr5 | 80255939 | ||||||
| chr5:80255951
|
G | C | 1 | a0001c0001t0075 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-29C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/12 | 29 | chr5 | 80255951 | |||||
| chr5:80255961
|
C | G | 2 | a0001c0001t0018a0001c0002t0031 | 3 | HG01168.hp2 HG01169.hp2 NA20752.hp2 |
5_prime_UTR_variant | MODIFIER | c.-39G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/12 | 39 | chr5 | 80255961 | |||||
| chr5:80255982
|
G | C | 2 | a0001c0001t0076a0001c0002t0077 | 2 | HG03239.hp1 HG04204.hp2 |
5_prime_UTR_variant | MODIFIER | c.-60C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/12 | 60 | chr5 | 80255982 | |||||
| chr5:80256048
|
A | G | 87 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(84): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
5_prime_UTR_variant | MODIFIER | c.-126T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/12 | 126 | chr5 | 80256048 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:80143937
|
C | T | 3 | a0001c0001t0040g0066a0001c0001t0042g0065a0001c0006t0020g0127 | 3 | HG02451.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1239-127G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80143937 | ||||||
| chr5:80143957
|
C | T | 1 | a0001c0001t0004g0084 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1239-147G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80143957 | ||||||
| chr5:80144037
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1239-227G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80144037 | ||||||
| chr5:80144395
|
T | C | 2 | a0001c0001t0011g0123a0001c0001t0011g0245 | 2 | HG01106.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1239-585A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80144395 | ||||||
| chr5:80144759
|
G | A | 2 | a0001c0001t0030g0255a0001c0001t0030g0257 | 2 | HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1239-949C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80144759 | ||||||
| chr5:80144952
|
C | T | 2 | a0001c0001t0030g0255a0001c0001t0030g0257 | 2 | HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1238+1138G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80144952 | ||||||
| chr5:80144997
|
TA | T | 132 | a0001c0001t0002g0115a0001c0001t0006g0023a0001c0001t0006g0064others(129): Show | 132 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1238+1092delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80144997 | ||||||
| chr5:80145027
|
T | C | 1 | a0001c0002t0031g0001 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1238+1063A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80145027 | ||||||
| chr5:80145046
|
T | TA | 6 | a0001c0001t0056g0198a0001c0009t0035g0209a0002c0003t0004g0118others(3): Show | 6 | HG00639.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.1238+1043dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80145046 | ||||||
| chr5:80145137
|
G | A | 2 | a0001c0001t0030g0255a0001c0001t0030g0257 | 2 | HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1238+953C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80145137 | ||||||
| chr5:80145188
|
A | T | 2 | a0001c0001t0006g0064a0002c0003t0009g0228 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1238+902T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80145188 | ||||||
| chr5:80145271
|
G | A | 4 | a0001c0001t0029g0102a0001c0001t0029g0144a0001c0001t0051g0236others(1): Show | 4 | HG02257.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238+819C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80145271 | ||||||
| chr5:80145302
|
C | G | 2 | a0001c0001t0009g0208a0001c0001t0048g0143 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1238+788G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80145302 | ||||||
| chr5:80145357
|
C | T | 2 | a0001c0001t0030g0255a0001c0001t0030g0257 | 2 | HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1238+733G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80145357 | ||||||
| chr5:80145362
|
G | T | 2 | a0001c0001t0030g0255a0001c0001t0030g0257 | 2 | HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1238+728C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80145362 | ||||||
| chr5:80145436
|
C | T | 1 | a0001c0002t0003g0035 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1238+654G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80145436 | ||||||
| chr5:80145516
|
T | C | 1 | a0001c0001t0059g0059 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1238+574A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80145516 | ||||||
| chr5:80146008
|
TCAAA | T | 7 | a0001c0001t0010g0062a0001c0001t0010g0183a0001c0001t0010g0235others(4): Show | 7 | HG01884.hp1 HG02109.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1238+78_1238+81del others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 11/11 | chr5 | 80146008 | ||||||
| chr5:80146428
|
GA | G | 4 | a0001c0001t0013g0068a0001c0001t0013g0140a0001c0001t0043g0234others(1): Show | 4 | HG02258.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1094-195delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 10/11 | chr5 | 80146428 | ||||||
| chr5:80146444
|
C | A | 19 | a0001c0001t0008g0125a0001c0001t0008g0129a0001c0001t0008g0182others(16): Show | 19 | HG01496.hp1 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1094-210G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 10/11 | chr5 | 80146444 | ||||||
| chr5:80146457
|
T | A | 19 | a0001c0001t0008g0125a0001c0001t0008g0129a0001c0001t0008g0182others(16): Show | 19 | HG01496.hp1 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1094-223A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 10/11 | chr5 | 80146457 | ||||||
| chr5:80146497
|
G | A | 1 | a0001c0001t0023g0130 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1094-263C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 10/11 | chr5 | 80146497 | ||||||
| chr5:80146578
|
A | G | 30 | a0001c0001t0008g0125a0001c0001t0008g0129a0001c0001t0008g0182others(27): Show | 30 | HG01496.hp1 HG01884.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1094-344T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 10/11 | chr5 | 80146578 | ||||||
| chr5:80146601
|
C | T | 1 | a0001c0001t0065g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1094-367G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 10/11 | chr5 | 80146601 | ||||||
| chr5:80146610
|
G | A | 2 | a0001c0002t0005g0105a0001c0002t0005g0122 | 2 | NA18955.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1094-376C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 10/11 | chr5 | 80146610 | ||||||
| chr5:80146715
|
C | G | 8 | a0001c0001t0008g0240a0001c0001t0008g0259a0001c0001t0020g0057others(5): Show | 8 | HG02451.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1094-481G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 10/11 | chr5 | 80146715 | ||||||
| chr5:80146753
|
C | G | 33 | a0001c0001t0008g0125a0001c0001t0008g0129a0001c0001t0008g0182others(30): Show | 33 | HG01167.hp2 HG01496.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.1093+492G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 10/11 | chr5 | 80146753 | ||||||
| chr5:80146763
|
T | C | 2 | a0001c0001t0010g0183a0001c0001t0050g0265 | 2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1093+482A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 10/11 | chr5 | 80146763 | ||||||
| chr5:80146976
|
GCT | G | 4 | a0001c0001t0033g0060a0001c0001t0044g0149a0001c0001t0046g0260others(1): Show | 4 | HG01167.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1093+267_1093+268d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 10/11 | chr5 | 80146976 | ||||||
| chr5:80147042
|
C | T | 2 | a0001c0001t0009g0208a0001c0001t0048g0143 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1093+203G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 10/11 | chr5 | 80147042 | ||||||
| chr5:80147063
|
C | T | 2 | a0001c0001t0009g0208a0001c0001t0048g0143 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1093+182G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 10/11 | chr5 | 80147063 | ||||||
| chr5:80147104
|
G | A | 4 | a0001c0001t0013g0068a0001c0001t0013g0140a0001c0001t0043g0234others(1): Show | 4 | HG02258.hp2 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1093+141C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 10/11 | chr5 | 80147104 | ||||||
| chr5:80147217
|
G | A | 30 | a0001c0001t0008g0125a0001c0001t0008g0129a0001c0001t0008g0182others(27): Show | 30 | HG01167.hp2 HG01496.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1093+28C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 10/11 | chr5 | 80147217 | ||||||
| chr5:80147221
|
AAAG | A | 12 | a0001c0001t0010g0062a0001c0001t0010g0183a0001c0001t0010g0235others(9): Show | 12 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1093+21_1093+23del others(3): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 10/11 | chr5 | 80147221 | ||||||
| chr5:80147346
|
A | G | 273 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(270): Show | 273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.1054-62T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80147346 | ||||||
| chr5:80147349
|
A | G | 31 | a0001c0001t0008g0125a0001c0001t0008g0129a0001c0001t0008g0182others(28): Show | 31 | HG01167.hp2 HG01496.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1054-65T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80147349 | ||||||
| chr5:80147357
|
C | A | 2 | a0001c0001t0020g0057a0001c0001t0041g0279 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1054-73G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80147357 | ||||||
| chr5:80147375
|
C | T | 45 | a0001c0001t0013g0140a0001c0001t0043g0234a0001c0002t0003g0010others(42): Show | 45 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1054-91G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80147375 | ||||||
| chr5:80147379
|
G | GCCCTGAA others(10): Show |
31 | a0001c0001t0008g0125a0001c0001t0008g0129a0001c0001t0008g0182others(28): Show | 31 | HG01167.hp2 HG01496.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1054-96_1054-95ins others(17): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80147379 | ||||||
| chr5:80147512
|
A | G | 31 | a0001c0001t0008g0125a0001c0001t0008g0129a0001c0001t0008g0182others(28): Show | 31 | HG01167.hp2 HG01496.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1054-228T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80147512 | ||||||
| chr5:80147513
|
G | C | 31 | a0001c0001t0008g0125a0001c0001t0008g0129a0001c0001t0008g0182others(28): Show | 31 | HG01167.hp2 HG01496.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1054-229C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80147513 | ||||||
| chr5:80147599
|
C | CT | 12 | a0001c0001t0010g0062a0001c0001t0010g0183a0001c0001t0010g0235others(9): Show | 12 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1054-316dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80147599 | ||||||
| chr5:80147662
|
G | A | 1 | a0001c0001t0002g0104 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1054-378C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80147662 | ||||||
| chr5:80147693
|
TC | T | 19 | a0001c0001t0008g0125a0001c0001t0008g0129a0001c0001t0008g0182others(16): Show | 19 | HG01496.hp1 HG01891.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1054-410delG | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80147693 | ||||||
| chr5:80147800
|
C | A | 17 | a0001c0001t0008g0125a0001c0001t0008g0129a0001c0001t0008g0240others(14): Show | 17 | HG01891.hp1 HG02451.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.1054-516G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80147800 | ||||||
| chr5:80147849
|
C | T | 17 | a0001c0001t0008g0125a0001c0001t0008g0129a0001c0001t0008g0240others(14): Show | 17 | HG01891.hp1 HG02451.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.1054-565G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80147849 | ||||||
| chr5:80147905
|
G | A | 1 | a0001c0001t0057g0196 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1054-621C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80147905 | ||||||
| chr5:80147908
|
G | A | 26 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0103others(23): Show | 26 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1054-624C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80147908 | ||||||
| chr5:80147968
|
G | A | 3 | a0001c0001t0033g0060a0001c0001t0046g0260a0001c0001t0047g0261 | 3 | HG01167.hp2 HG03453.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1054-684C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80147968 | ||||||
| chr5:80148134
|
G | A | 18 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(15): Show | 18 | HG01891.hp1 HG02451.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1054-850C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148134 | ||||||
| chr5:80148182
|
TTTTATTC | T | 40 | a0001c0001t0013g0140a0001c0001t0030g0255a0001c0001t0030g0257others(37): Show | 40 | HG00438.hp1 HG00609.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.1054-905_1054-899d others(9): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148182 | ||||||
| chr5:80148183
|
TTTATTC | T | 6 | a0001c0001t0065g0132a0001c0002t0003g0222a0001c0002t0005g0122others(3): Show | 6 | HG00735.hp2 HG03239.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.1054-905_1054-900d others(8): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148183 | ||||||
| chr5:80148189
|
C | CT | 16 | a0001c0001t0001g0039a0001c0001t0010g0062a0001c0001t0010g0183others(13): Show | 16 | HG01884.hp1 HG02109.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.1054-906dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148189 | ||||||
| chr5:80148189
|
C | CTT | 14 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(11): Show | 14 | HG01891.hp1 HG02486.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1054-907_1054-906d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148189 | ||||||
| chr5:80148189
|
C | CTTTTTTT others(3): Show |
40 | a0001c0001t0001g0088a0001c0001t0001g0103a0001c0001t0001g0107others(37): Show | 40 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1054-915_1054-906d others(12): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148189 | ||||||
| chr5:80148189
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0046a0001c0001t0006g0064a0001c0001t0006g0114others(1): Show | 4 | HG00741.hp1 HG02004.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054-916_1054-906d others(13): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148189 | ||||||
| chr5:80148189
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0009g0139a0001c0001t0009g0208a0001c0001t0048g0143others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054-917_1054-906d others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148189 | ||||||
| chr5:80148189
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0009g0126a0001c0001t0075g0284 | 2 | HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1054-918_1054-906d others(15): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148189 | ||||||
| chr5:80148224
|
C | G | 107 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0103others(104): Show | 107 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1054-940G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148224 | ||||||
| chr5:80148278
|
C | A | 1 | a0001c0001t0030g0257 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1054-994G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148278 | ||||||
| chr5:80148302
|
T | C | 3 | a0001c0001t0033g0060a0001c0001t0046g0260a0001c0001t0047g0261 | 3 | HG01167.hp2 HG03453.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1054-1018A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148302 | ||||||
| chr5:80148459
|
G | A | 13 | a0001c0001t0010g0062a0001c0001t0010g0183a0001c0001t0010g0235others(10): Show | 13 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1054-1175C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148459 | ||||||
| chr5:80148470
|
G | A | 18 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(15): Show | 18 | HG01891.hp1 HG02451.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1054-1186C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148470 | ||||||
| chr5:80148482
|
A | G | 31 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(28): Show | 31 | HG01167.hp2 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.1054-1198T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148482 | ||||||
| chr5:80148550
|
C | T | 13 | a0001c0001t0010g0062a0001c0001t0010g0183a0001c0001t0010g0235others(10): Show | 13 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1054-1266G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148550 | ||||||
| chr5:80148586
|
T | G | 52 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0103others(49): Show | 52 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1054-1302A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148586 | ||||||
| chr5:80148641
|
C | G | 2 | a0001c0002t0003g0096a0001c0002t0005g0095 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1054-1357G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148641 | ||||||
| chr5:80148667
|
C | CA | 29 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0103others(26): Show | 29 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1054-1384dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148667 | ||||||
| chr5:80148667
|
CAA | C | 13 | a0001c0001t0010g0062a0001c0001t0010g0183a0001c0001t0010g0235others(10): Show | 13 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1054-1385_1054-138 others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148667 | ||||||
| chr5:80148697
|
G | A | 13 | a0001c0001t0010g0062a0001c0001t0010g0183a0001c0001t0010g0235others(10): Show | 13 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1054-1413C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148697 | ||||||
| chr5:80148763
|
C | T | 1 | a0001c0001t0055g0276 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1054-1479G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148763 | ||||||
| chr5:80148860
|
C | T | 1 | a0001c0001t0001g0006 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1054-1576G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148860 | ||||||
| chr5:80148861
|
C | T | 45 | a0001c0001t0013g0140a0001c0001t0043g0234a0001c0002t0003g0010others(42): Show | 45 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1054-1577G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80148861 | ||||||
| chr5:80149003
|
G | A | 18 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(15): Show | 18 | HG01891.hp1 HG02451.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1054-1719C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80149003 | ||||||
| chr5:80149045
|
T | C | 5 | a0001c0001t0008g0240a0001c0001t0008g0259a0001c0001t0037g0262others(2): Show | 5 | HG03225.hp2 NA19030.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054-1761A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80149045 | ||||||
| chr5:80149135
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1053+1747A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80149135 | ||||||
| chr5:80149366
|
G | T | 2 | a0001c0001t0059g0059a0001c0002t0005g0058 | 2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1053+1516C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80149366 | ||||||
| chr5:80149389
|
A | AT | 285 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1053+1492dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80149389 | ||||||
| chr5:80149545
|
C | T | 4 | a0001c0001t0013g0067a0001c0002t0022g0272a0002c0003t0004g0118others(1): Show | 4 | HG00639.hp2 HG01106.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053+1337G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80149545 | ||||||
| chr5:80149745
|
G | A | 10 | a0001c0001t0010g0062a0001c0001t0010g0183a0001c0001t0010g0235others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1053+1137C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80149745 | ||||||
| chr5:80149776
|
G | A | 4 | a0001c0001t0013g0068a0001c0001t0030g0255a0001c0001t0030g0257others(1): Show | 4 | HG02895.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053+1106C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80149776 | ||||||
| chr5:80150136
|
T | C | 1 | a0001c0002t0031g0001 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1053+746A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80150136 | ||||||
| chr5:80150264
|
C | T | 1 | a0001c0006t0045g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1053+618G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80150264 | ||||||
| chr5:80150279
|
G | A | 44 | a0001c0001t0006g0023a0001c0001t0006g0064a0001c0001t0006g0114others(41): Show | 44 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1053+603C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80150279 | ||||||
| chr5:80150369
|
C | G | 2 | a0001c0002t0005g0105a0001c0002t0005g0122 | 2 | NA18955.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1053+513G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80150369 | ||||||
| chr5:80150690
|
A | C | 31 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(28): Show | 31 | HG01167.hp2 HG01884.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.1053+192T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80150690 | ||||||
| chr5:80150706
|
G | A | 3 | a0001c0001t0030g0255a0001c0001t0030g0257a0001c0001t0034g0207 | 3 | HG03130.hp1 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1053+176C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80150706 | ||||||
| chr5:80150720
|
G | T | 1 | a0001c0001t0057g0196 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1053+162C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80150720 | ||||||
| chr5:80150729
|
C | T | 1 | a0001c0002t0003g0040 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1053+153G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80150729 | ||||||
| chr5:80150732
|
G | A | 18 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(15): Show | 18 | HG01891.hp1 HG02451.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1053+150C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80150732 | ||||||
| chr5:80150792
|
T | C | 3 | a0001c0001t0009g0126a0001c0001t0009g0139a0001c0001t0075g0284 | 3 | HG02280.hp1 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1053+90A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80150792 | ||||||
| chr5:80150820
|
A | G | 1 | a0001c0001t0009g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1053+62T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80150820 | ||||||
| chr5:80150836
|
T | C | 10 | a0001c0001t0010g0062a0001c0001t0010g0183a0001c0001t0010g0235others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1053+46A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 9/11 | chr5 | 80150836 | ||||||
| chr5:80150988
|
C | A | 22 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(19): Show | 22 | HG00639.hp2 HG01106.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.987-40G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80150988 | ||||||
| chr5:80151019
|
G | A | 3 | a0001c0001t0030g0255a0001c0001t0030g0257a0001c0001t0034g0207 | 3 | HG03130.hp1 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.987-71C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151019 | ||||||
| chr5:80151044
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.987-96G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151044 | ||||||
| chr5:80151060
|
G | A | 1 | a0001c0001t0009g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.987-112C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151060 | ||||||
| chr5:80151081
|
G | A | 44 | a0001c0001t0006g0023a0001c0001t0006g0064a0001c0001t0006g0114others(41): Show | 44 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.987-133C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151081 | ||||||
| chr5:80151089
|
T | C | 1 | a0001c0002t0005g0137 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.987-141A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151089 | ||||||
| chr5:80151157
|
G | A | 13 | a0001c0001t0010g0062a0001c0001t0010g0183a0001c0001t0010g0235others(10): Show | 13 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.987-209C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151157 | ||||||
| chr5:80151350
|
A | G | 7 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(4): Show | 7 | HG01891.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.987-402T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151350 | ||||||
| chr5:80151358
|
A | T | 1 | a0001c0001t0021g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.987-410T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151358 | ||||||
| chr5:80151421
|
G | A | 13 | a0001c0001t0010g0062a0001c0001t0010g0183a0001c0001t0010g0235others(10): Show | 13 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.987-473C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151421 | ||||||
| chr5:80151481
|
G | A | 4 | a0001c0001t0013g0067a0001c0002t0022g0272a0002c0003t0004g0118others(1): Show | 4 | HG00639.hp2 HG01106.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.987-533C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151481 | ||||||
| chr5:80151483
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.987-535A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151483 | ||||||
| chr5:80151568
|
ACT | A | 35 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(32): Show | 35 | HG00639.hp2 HG01106.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.987-622_987-621del others(2): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151568 | ||||||
| chr5:80151590
|
G | T | 35 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(32): Show | 35 | HG00639.hp2 HG01106.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.987-642C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151590 | ||||||
| chr5:80151626
|
G | A | 13 | a0001c0001t0010g0062a0001c0001t0010g0183a0001c0001t0010g0235others(10): Show | 13 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.987-678C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151626 | ||||||
| chr5:80151657
|
A | G | 1 | a0001c0002t0073g0204 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.987-709T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151657 | ||||||
| chr5:80151679
|
A | G | 1 | a0001c0001t0002g0278 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.987-731T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151679 | ||||||
| chr5:80151762
|
C | T | 18 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(15): Show | 18 | HG01891.hp1 HG02451.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.987-814G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151762 | ||||||
| chr5:80151807
|
C | T | 69 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(66): Show | 69 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.987-859G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80151807 | ||||||
| chr5:80152173
|
C | T | 7 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(4): Show | 7 | HG01891.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.987-1225G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80152173 | ||||||
| chr5:80152259
|
G | T | 46 | a0001c0001t0001g0177a0001c0001t0006g0023a0001c0001t0006g0064others(43): Show | 46 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.987-1311C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80152259 | ||||||
| chr5:80152364
|
G | A | 22 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(19): Show | 22 | HG00639.hp2 HG01106.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.987-1416C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80152364 | ||||||
| chr5:80152491
|
C | CA | 50 | a0001c0001t0013g0140a0001c0001t0030g0255a0001c0001t0030g0257others(47): Show | 50 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.987-1544dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80152491 | ||||||
| chr5:80152491
|
CA | C | 11 | a0001c0001t0001g0092a0001c0001t0001g0103a0001c0001t0002g0097others(8): Show | 11 | HG00639.hp2 HG01069.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.987-1544delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80152491 | ||||||
| chr5:80152491
|
CAA | C | 30 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(27): Show | 30 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.987-1545_987-1544d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80152491 | ||||||
| chr5:80152491
|
CAAAA | C | 10 | a0001c0001t0001g0177a0001c0002t0003g0168a0001c0002t0003g0184others(7): Show | 10 | HG00323.hp1 HG00621.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.987-1547_987-1544d others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80152491 | ||||||
| chr5:80152550
|
G | T | 1 | a0001c0001t0002g0018 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.987-1602C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80152550 | ||||||
| chr5:80152620
|
T | C | 1 | a0001c0001t0065g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.987-1672A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80152620 | ||||||
| chr5:80152627
|
G | T | 4 | a0001c0001t0013g0067a0001c0002t0022g0272a0002c0003t0004g0118others(1): Show | 4 | HG00639.hp2 HG01106.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.987-1679C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80152627 | ||||||
| chr5:80152774
|
A | C | 77 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(74): Show | 77 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.987-1826T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80152774 | ||||||
| chr5:80152831
|
C | T | 21 | a0001c0001t0007g0150a0001c0001t0008g0125a0001c0001t0008g0129others(18): Show | 21 | HG00639.hp2 HG01106.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.987-1883G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80152831 | ||||||
| chr5:80152898
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.987-1950G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80152898 | ||||||
| chr5:80153008
|
C | T | 1 | a0001c0001t0065g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.987-2060G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80153008 | ||||||
| chr5:80153052
|
T | C | 1 | a0001c0001t0004g0138 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.987-2104A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80153052 | ||||||
| chr5:80153076
|
C | G | 82 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(79): Show | 82 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.987-2128G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80153076 | ||||||
| chr5:80153165
|
C | T | 6 | a0001c0001t0015g0063a0001c0001t0015g0256a0001c0001t0015g0258others(3): Show | 6 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.987-2217G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80153165 | ||||||
| chr5:80153181
|
G | T | 8 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(5): Show | 8 | HG01243.hp2 HG01891.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.987-2233C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80153181 | ||||||
| chr5:80153276
|
G | T | 47 | a0001c0001t0001g0030a0001c0001t0001g0177a0001c0001t0002g0094others(44): Show | 47 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.987-2328C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80153276 | ||||||
| chr5:80153331
|
G | A | 53 | a0001c0001t0010g0062a0001c0001t0010g0183a0001c0001t0010g0235others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.987-2383C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80153331 | ||||||
| chr5:80153350
|
C | T | 2 | a0001c0001t0021g0053a0001c0001t0021g0141 | 2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.987-2402G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80153350 | ||||||
| chr5:80153392
|
A | G | 22 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(19): Show | 22 | HG00639.hp2 HG01106.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.987-2444T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80153392 | ||||||
| chr5:80153464
|
T | C | 1 | a0001c0001t0002g0104 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.987-2516A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80153464 | ||||||
| chr5:80153474
|
GT | G | 82 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(79): Show | 82 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.987-2527delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80153474 | ||||||
| chr5:80153549
|
T | G | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.987-2601A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80153549 | ||||||
| chr5:80153702
|
A | T | 4 | a0001c0001t0013g0067a0001c0002t0022g0272a0002c0003t0004g0118others(1): Show | 4 | HG00639.hp2 HG01106.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.987-2754T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80153702 | ||||||
| chr5:80153704
|
G | A | 4 | a0001c0001t0008g0259a0001c0001t0030g0255a0001c0001t0030g0257others(1): Show | 4 | HG03130.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.987-2756C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80153704 | ||||||
| chr5:80153808
|
C | CA | 7 | a0001c0001t0004g0052a0001c0001t0006g0064a0001c0001t0008g0125others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.987-2861dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80153808 | ||||||
| chr5:80153983
|
C | T | 2 | a0001c0001t0020g0057a0001c0001t0041g0279 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.987-3035G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80153983 | ||||||
| chr5:80154056
|
G | A | 83 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(80): Show | 83 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.987-3108C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80154056 | ||||||
| chr5:80154246
|
G | A | 57 | a0001c0001t0010g0062a0001c0001t0010g0183a0001c0001t0010g0235others(54): Show | 57 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.987-3298C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80154246 | ||||||
| chr5:80154304
|
C | T | 57 | a0001c0001t0010g0062a0001c0001t0010g0183a0001c0001t0010g0235others(54): Show | 57 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.987-3356G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80154304 | ||||||
| chr5:80154321
|
A | G | 4 | a0001c0001t0029g0102a0001c0001t0029g0144a0001c0001t0051g0236others(1): Show | 4 | HG02257.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-3373T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80154321 | ||||||
| chr5:80154466
|
A | G | 1 | a0001c0001t0002g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.987-3518T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80154466 | ||||||
| chr5:80154470
|
C | T | 4 | a0001c0001t0029g0102a0001c0001t0029g0144a0001c0001t0051g0236others(1): Show | 4 | HG02257.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-3522G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80154470 | ||||||
| chr5:80154552
|
C | T | 83 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(80): Show | 83 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.987-3604G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80154552 | ||||||
| chr5:80154601
|
C | A | 2 | a0001c0001t0004g0020a0001c0001t0004g0021 | 2 | HG00639.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.987-3653G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80154601 | ||||||
| chr5:80154602
|
C | T | 2 | a0001c0001t0013g0140a0001c0001t0043g0234 | 2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.987-3654G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80154602 | ||||||
| chr5:80154905
|
T | C | 2 | a0001c0001t0013g0140a0001c0001t0043g0234 | 2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.986+3931A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80154905 | ||||||
| chr5:80154968
|
A | T | 1 | a0001c0001t0008g0259 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.986+3868T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80154968 | ||||||
| chr5:80155261
|
C | T | 2 | a0001c0001t0013g0140a0001c0001t0043g0234 | 2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.986+3575G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155261 | ||||||
| chr5:80155264
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.986+3572G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155264 | ||||||
| chr5:80155336
|
G | A | 22 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(19): Show | 22 | HG00639.hp2 HG01106.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.986+3500C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155336 | ||||||
| chr5:80155376
|
C | T | 4 | a0001c0001t0029g0102a0001c0001t0029g0144a0001c0001t0051g0236others(1): Show | 4 | HG02257.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.986+3460G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155376 | ||||||
| chr5:80155393
|
C | T | 1 | a0001c0002t0005g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.986+3443G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155393 | ||||||
| chr5:80155434
|
G | A | 18 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(15): Show | 18 | HG01243.hp2 HG01891.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.986+3402C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155434 | ||||||
| chr5:80155567
|
C | T | 2 | a0001c0001t0059g0059a0001c0002t0005g0058 | 2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.986+3269G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155567 | ||||||
| chr5:80155572
|
C | CAAAAAAA others(2): Show |
7 | a0001c0001t0018g0002a0001c0001t0029g0102a0001c0001t0029g0144others(4): Show | 7 | HG01070.hp1 HG01168.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.986+3255_986+3263d others(11): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155572 | ||||||
| chr5:80155572
|
C | CAAAAAAA others(3): Show |
102 | a0001c0001t0001g0030a0001c0001t0001g0177a0001c0001t0002g0094others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.986+3254_986+3263d others(12): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155572 | ||||||
| chr5:80155572
|
C | CAAAAAAA others(4): Show |
18 | a0001c0001t0009g0126a0001c0001t0013g0067a0001c0001t0020g0057others(15): Show | 18 | HG00609.hp1 HG00639.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.986+3253_986+3263d others(13): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155572 | ||||||
| chr5:80155572
|
C | CAAAAAAA others(5): Show |
7 | a0001c0001t0006g0064a0001c0001t0009g0139a0001c0001t0037g0262others(4): Show | 7 | HG01167.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.986+3263_986+3264i others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155572 | ||||||
| chr5:80155572
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0008g0240a0001c0001t0046g0260a0002c0003t0009g0228 | 3 | HG02486.hp2 NA19240.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.986+3263_986+3264i others(15): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155572 | ||||||
| chr5:80155592
|
G | A | 1 | a0001c0002t0017g0145 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.986+3244C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155592 | ||||||
| chr5:80155595
|
G | GGA | 4 | a0001c0001t0008g0259a0001c0001t0030g0255a0001c0001t0030g0257others(1): Show | 4 | HG03130.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.986+3239_986+3240d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155595 | ||||||
| chr5:80155610
|
G | GAGAA | 4 | a0001c0001t0029g0102a0001c0001t0029g0144a0001c0001t0051g0236others(1): Show | 4 | HG02257.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.986+3225_986+3226i others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155610 | ||||||
| chr5:80155661
|
T | C | 1 | a0001c0001t0013g0068 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.986+3175A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155661 | ||||||
| chr5:80155804
|
G | T | 19 | a0001c0001t0001g0177a0001c0002t0003g0168a0001c0002t0003g0184others(16): Show | 19 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.986+3032C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155804 | ||||||
| chr5:80155937
|
G | C | 1 | a0001c0006t0045g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.986+2899C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80155937 | ||||||
| chr5:80156055
|
G | A | 2 | a0001c0002t0027g0148a0001c0002t0027g0274 | 2 | HG01884.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.986+2781C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156055 | ||||||
| chr5:80156096
|
A | T | 2 | a0001c0001t0020g0057a0001c0001t0041g0279 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.986+2740T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156096 | ||||||
| chr5:80156131
|
T | G | 53 | a0001c0001t0010g0062a0001c0001t0010g0183a0001c0001t0010g0235others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.986+2705A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156131 | ||||||
| chr5:80156132
|
T | C | 53 | a0001c0001t0010g0062a0001c0001t0010g0183a0001c0001t0010g0235others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.986+2704A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156132 | ||||||
| chr5:80156206
|
C | G | 8 | a0001c0001t0013g0067a0001c0001t0029g0102a0001c0001t0029g0144others(5): Show | 8 | HG00639.hp2 HG01106.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.986+2630G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156206 | ||||||
| chr5:80156317
|
C | T | 1 | a0001c0006t0020g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.986+2519G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156317 | ||||||
| chr5:80156331
|
C | T | 2 | a0001c0001t0013g0140a0001c0001t0043g0234 | 2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.986+2505G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156331 | ||||||
| chr5:80156393
|
G | C | 1 | a0001c0001t0056g0198 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.986+2443C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156393 | ||||||
| chr5:80156524
|
T | C | 2 | a0001c0001t0013g0140a0001c0001t0043g0234 | 2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.986+2312A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156524 | ||||||
| chr5:80156536
|
G | C | 101 | a0001c0001t0001g0177a0001c0001t0002g0277a0001c0001t0007g0150others(98): Show | 101 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.986+2300C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156536 | ||||||
| chr5:80156645
|
T | C | 28 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(25): Show | 28 | HG00639.hp2 HG01106.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.986+2191A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156645 | ||||||
| chr5:80156811
|
G | C | 28 | a0001c0001t0001g0030a0001c0001t0002g0094a0001c0001t0006g0023others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.986+2025C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156811 | ||||||
| chr5:80156905
|
A | G | 4 | a0001c0001t0008g0259a0001c0001t0030g0255a0001c0001t0030g0257others(1): Show | 4 | HG03130.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.986+1931T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156905 | ||||||
| chr5:80156910
|
G | A | 2 | a0001c0001t0001g0269a0001c0001t0002g0270 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.986+1926C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156910 | ||||||
| chr5:80156986
|
T | C | 1 | a0001c0001t0065g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.986+1850A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156986 | ||||||
| chr5:80156991
|
TTC | T | 6 | a0001c0001t0013g0067a0001c0001t0013g0068a0001c0001t0033g0060others(3): Show | 6 | HG00639.hp2 HG01106.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.986+1843_986+1844d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156991 | ||||||
| chr5:80156993
|
C | CT | 8 | a0001c0001t0001g0194a0001c0001t0001g0213a0001c0001t0002g0018others(5): Show | 8 | HG01074.hp1 HG01099.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.986+1842dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156993 | ||||||
| chr5:80156993
|
C | CTT | 61 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(58): Show | 61 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.986+1841_986+1842d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156993 | ||||||
| chr5:80156993
|
CT | C | 80 | a0001c0001t0001g0177a0001c0001t0002g0112a0001c0001t0009g0126others(77): Show | 80 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.986+1842delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156993 | ||||||
| chr5:80156993
|
CTT | C | 11 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(8): Show | 11 | HG01243.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.986+1841_986+1842d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156993 | ||||||
| chr5:80156993
|
CTTT | C | 9 | a0001c0001t0020g0057a0001c0001t0029g0102a0001c0001t0029g0144others(6): Show | 9 | HG02257.hp1 HG03041.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.986+1840_986+1842d others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156993 | ||||||
| chr5:80156996
|
T | C | 11 | a0001c0001t0008g0240a0001c0001t0013g0067a0001c0001t0013g0068others(8): Show | 11 | HG00639.hp2 HG01106.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.986+1840A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80156996 | ||||||
| chr5:80157054
|
G | A | 2 | a0001c0001t0009g0208a0001c0001t0048g0143 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.986+1782C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80157054 | ||||||
| chr5:80157081
|
C | G | 2 | a0001c0002t0003g0096a0001c0002t0005g0095 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.986+1755G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80157081 | ||||||
| chr5:80157117
|
G | A | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.986+1719C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80157117 | ||||||
| chr5:80157196
|
T | C | 1 | a0001c0001t0058g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.986+1640A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80157196 | ||||||
| chr5:80157272
|
C | T | 1 | a0001c0006t0045g0128 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.986+1564G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80157272 | ||||||
| chr5:80157284
|
C | T | 1 | a0001c0001t0014g0086 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.986+1552G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80157284 | ||||||
| chr5:80157297
|
G | C | 1 | a0001c0001t0004g0221 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.986+1539C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80157297 | ||||||
| chr5:80157303
|
AT | A | 20 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(17): Show | 20 | HG01167.hp2 HG01243.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.986+1532delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80157303 | ||||||
| chr5:80157314
|
T | C | 20 | a0001c0001t0001g0177a0001c0001t0055g0276a0001c0002t0003g0168others(17): Show | 20 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.986+1522A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80157314 | ||||||
| chr5:80157324
|
A | C | 28 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(25): Show | 28 | HG00639.hp2 HG01106.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.986+1512T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80157324 | ||||||
| chr5:80157370
|
T | C | 1 | a0001c0010t0005g0223 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.986+1466A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80157370 | ||||||
| chr5:80157522
|
A | AT | 18 | a0001c0001t0008g0240a0001c0001t0013g0067a0001c0001t0020g0057others(15): Show | 18 | HG00639.hp2 HG01106.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.986+1313dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80157522 | ||||||
| chr5:80157551
|
C | CT | 285 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.986+1284dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80157551 | ||||||
| chr5:80157684
|
C | T | 2 | a0001c0001t0006g0064a0002c0003t0009g0228 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.986+1152G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80157684 | ||||||
| chr5:80157904
|
T | C | 6 | a0001c0001t0013g0067a0001c0001t0013g0068a0001c0001t0033g0060others(3): Show | 6 | HG00639.hp2 HG01106.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.986+932A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80157904 | ||||||
| chr5:80158071
|
T | G | 1 | a0001c0001t0058g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.986+765A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80158071 | ||||||
| chr5:80158243
|
G | C | 3 | a0001c0009t0035g0209a0002c0005t0019g0042a0002c0005t0019g0273 | 3 | HG03139.hp1 HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.986+593C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80158243 | ||||||
| chr5:80158394
|
C | T | 11 | a0001c0001t0006g0023a0001c0001t0006g0114a0001c0001t0006g0135others(8): Show | 11 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.986+442G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80158394 | ||||||
| chr5:80158429
|
C | T | 47 | a0001c0001t0001g0177a0001c0001t0002g0277a0001c0001t0007g0150others(44): Show | 47 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.986+407G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80158429 | ||||||
| chr5:80158676
|
G | A | 10 | a0001c0001t0008g0240a0001c0001t0020g0057a0001c0001t0037g0262others(7): Show | 10 | HG02451.hp2 HG03041.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.986+160C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80158676 | ||||||
| chr5:80158726
|
T | TC | 8 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(5): Show | 8 | HG01243.hp2 HG01891.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.986+109dupG | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80158726 | ||||||
| chr5:80158811
|
A | G | 49 | a0001c0001t0001g0177a0001c0001t0002g0277a0001c0001t0007g0150others(46): Show | 49 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.986+25T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 8/11 | chr5 | 80158811 | ||||||
| chr5:80159259
|
T | G | 2 | a0001c0001t0009g0208a0001c0001t0048g0143 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.860-297A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80159259 | ||||||
| chr5:80159275
|
C | G | 4 | a0001c0001t0008g0259a0001c0001t0030g0255a0001c0001t0030g0257others(1): Show | 4 | HG03130.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.860-313G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80159275 | ||||||
| chr5:80159451
|
T | C | 1 | a0001c0010t0005g0223 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.860-489A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80159451 | ||||||
| chr5:80159501
|
T | A | 3 | a0001c0001t0002g0109a0001c0001t0002g0280a0001c0001t0007g0281 | 3 | HG02572.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.860-539A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80159501 | ||||||
| chr5:80159582
|
C | T | 1 | a0001c0001t0004g0247 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.860-620G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80159582 | ||||||
| chr5:80159824
|
C | T | 1 | a0001c0001t0011g0123 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.860-862G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80159824 | ||||||
| chr5:80159840
|
T | C | 1 | a0001c0001t0026g0070 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.860-878A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80159840 | ||||||
| chr5:80159969
|
A | G | 27 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0103others(24): Show | 27 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.860-1007T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80159969 | ||||||
| chr5:80159975
|
A | G | 7 | a0001c0001t0008g0240a0001c0001t0020g0057a0001c0001t0037g0262others(4): Show | 7 | HG02451.hp2 HG03041.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.860-1013T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80159975 | ||||||
| chr5:80160162
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0060g0017 | 2 | HG02129.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.860-1200G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160162 | ||||||
| chr5:80160166
|
T | C | 1 | a0001c0001t0009g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.860-1204A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160166 | ||||||
| chr5:80160264
|
T | C | 17 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0052others(14): Show | 17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.860-1302A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160264 | ||||||
| chr5:80160361
|
A | G | 1 | a0001c0001t0013g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.860-1399T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160361 | ||||||
| chr5:80160366
|
G | A | 27 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(24): Show | 27 | HG00639.hp2 HG01106.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.860-1404C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160366 | ||||||
| chr5:80160396
|
G | A | 1 | a0001c0001t0061g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.860-1434C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160396 | ||||||
| chr5:80160400
|
G | A | 2 | a0001c0001t0065g0132a0001c0006t0045g0128 | 2 | HG00735.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.860-1438C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160400 | ||||||
| chr5:80160512
|
T | G | 2 | a0001c0001t0013g0140a0001c0001t0043g0234 | 2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.860-1550A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160512 | ||||||
| chr5:80160610
|
G | A | 20 | a0001c0001t0001g0177a0001c0001t0055g0276a0001c0002t0003g0168others(17): Show | 20 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.860-1648C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160610 | ||||||
| chr5:80160737
|
T | G | 1 | a0001c0001t0006g0135 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.860-1775A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160737 | ||||||
| chr5:80160920
|
ATG | A | 86 | a0001c0001t0001g0030a0001c0001t0001g0046a0001c0001t0001g0088others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.860-1960_860-1959d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160920 | ||||||
| chr5:80160932
|
GTGTATAT others(11): Show |
G | 3 | a0001c0001t0013g0067a0002c0003t0004g0118a0002c0003t0011g0119 | 3 | HG00639.hp2 HG01106.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.860-1988_860-1971d others(20): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160932 | ||||||
| chr5:80160956
|
A | ATG | 37 | a0001c0001t0007g0249a0001c0001t0032g0004a0001c0002t0003g0010others(34): Show | 37 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.860-1996_860-1995d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160956 | ||||||
| chr5:80160964
|
G | A | 3 | a0001c0001t0013g0067a0002c0003t0004g0118a0002c0003t0011g0119 | 3 | HG00639.hp2 HG01106.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.860-2002C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160964 | ||||||
| chr5:80160964
|
G | GTA | 86 | a0001c0001t0001g0030a0001c0001t0001g0046a0001c0001t0001g0088others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.860-2004_860-2003d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160964 | ||||||
| chr5:80160973
|
T | TAC | 4 | a0001c0001t0008g0259a0001c0001t0030g0255a0001c0001t0030g0257others(1): Show | 4 | HG03130.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.860-2012_860-2011i others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160973 | ||||||
| chr5:80160977
|
T | A | 27 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(24): Show | 27 | HG00639.hp2 HG01106.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.860-2015A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160977 | ||||||
| chr5:80160983
|
T | TGTGTATA others(25): Show |
25 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0103others(22): Show | 25 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.860-2053_860-2022d others(34): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160983 | ||||||
| chr5:80160990
|
ATG | A | 13 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(10): Show | 13 | HG01243.hp2 HG01891.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.860-2030_860-2029d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160990 | ||||||
| chr5:80160991
|
T | TGTATATA others(25): Show |
1 | a0002c0004t0005g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.860-2030_860-2029i others(34): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160991 | ||||||
| chr5:80160992
|
G | A | 4 | a0001c0001t0008g0240a0001c0001t0037g0262a0001c0001t0038g0111others(1): Show | 4 | NA19030.hp2 NA19240.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.860-2030C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160992 | ||||||
| chr5:80160994
|
ATATATAT others(5): Show |
A | 3 | a0001c0002t0003g0146a0001c0002t0003g0147a0001c0002t0003g0192 | 3 | NA18942.hp1 NA18969.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.860-2044_860-2033d others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80160994 | ||||||
| chr5:80161013
|
T | TACGTGTA others(11): Show |
4 | a0001c0001t0002g0047a0001c0001t0002g0097a0001c0001t0002g0098others(1): Show | 4 | HG01074.hp2 HG01346.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.860-2069_860-2052d others(20): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161013 | ||||||
| chr5:80161014
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.860-2052T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161014 | ||||||
| chr5:80161022
|
ATATATAC others(7): Show |
A | 15 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(12): Show | 15 | HG01167.hp2 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.860-2074_860-2061d others(16): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161022 | ||||||
| chr5:80161024
|
ATATACAC others(5): Show |
A | 18 | a0001c0001t0008g0240a0001c0001t0013g0067a0001c0001t0013g0068others(15): Show | 18 | HG00639.hp2 HG01106.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.860-2074_860-2063d others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161024 | ||||||
| chr5:80161029
|
C | T | 4 | a0001c0001t0008g0259a0001c0001t0030g0255a0001c0001t0030g0257others(1): Show | 4 | HG03130.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.860-2067G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161029 | ||||||
| chr5:80161031
|
C | T | 4 | a0001c0001t0008g0259a0001c0001t0030g0255a0001c0001t0030g0257others(1): Show | 4 | HG03130.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.860-2069G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161031 | ||||||
| chr5:80161036
|
G | GTA | 3 | a0001c0001t0007g0249a0001c0002t0003g0096a0001c0002t0005g0095 | 3 | HG00140.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.860-2076_860-2075d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161036 | ||||||
| chr5:80161036
|
G | GTATATAT others(7): Show |
4 | a0001c0001t0008g0259a0001c0001t0030g0255a0001c0001t0030g0257others(1): Show | 4 | HG03130.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.860-2075_860-2074i others(16): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161036 | ||||||
| chr5:80161044
|
A | G | 30 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(27): Show | 30 | HG00639.hp2 HG01106.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.860-2082T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161044 | ||||||
| chr5:80161046
|
A | ATG | 23 | a0001c0001t0001g0030a0001c0001t0002g0094a0001c0001t0006g0023others(20): Show | 23 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.860-2085_860-2084i others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161046 | ||||||
| chr5:80161046
|
A | G | 33 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(30): Show | 33 | HG00639.hp2 HG01106.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.860-2084T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161046 | ||||||
| chr5:80161048
|
A | ATGTG | 36 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0103others(33): Show | 36 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.860-2087_860-2086i others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161048 | ||||||
| chr5:80161048
|
A | G | 56 | a0001c0001t0001g0030a0001c0001t0002g0094a0001c0001t0002g0277others(53): Show | 56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.860-2086T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161048 | ||||||
| chr5:80161091
|
A | G | 1 | a0001c0001t0013g0068 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.860-2129T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161091 | ||||||
| chr5:80161152
|
G | T | 17 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(14): Show | 17 | HG01243.hp2 HG01891.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.860-2190C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161152 | ||||||
| chr5:80161385
|
C | CCA | 30 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(27): Show | 30 | HG00639.hp2 HG01106.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.860-2425_860-2424d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161385 | ||||||
| chr5:80161475
|
C | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0043a0001c0001t0001g0089others(6): Show | 9 | HG01109.hp2 HG01515.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.860-2513G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161475 | ||||||
| chr5:80161529
|
T | C | 30 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(27): Show | 30 | HG00639.hp2 HG01106.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.860-2567A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161529 | ||||||
| chr5:80161580
|
T | A | 94 | a0001c0001t0001g0030a0001c0001t0001g0046a0001c0001t0001g0088others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.860-2618A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161580 | ||||||
| chr5:80161701
|
A | C | 1 | a0001c0001t0050g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.860-2739T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161701 | ||||||
| chr5:80161772
|
T | C | 3 | a0001c0001t0002g0109a0001c0001t0002g0280a0001c0001t0007g0281 | 3 | HG02572.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.860-2810A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161772 | ||||||
| chr5:80161815
|
C | G | 4 | a0001c0001t0013g0140a0001c0001t0043g0234a0001c0001t0065g0132others(1): Show | 4 | HG00735.hp2 HG02258.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.860-2853G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161815 | ||||||
| chr5:80161845
|
G | A | 1 | a0001c0001t0010g0266 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.860-2883C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161845 | ||||||
| chr5:80161902
|
CAG | C | 11 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0052others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.860-2942_860-2941d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161902 | ||||||
| chr5:80161906
|
G | A | 7 | a0001c0001t0008g0240a0001c0001t0020g0057a0001c0001t0037g0262others(4): Show | 7 | HG02451.hp2 HG03041.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.860-2944C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80161906 | ||||||
| chr5:80162023
|
A | G | 1 | a0001c0006t0020g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.860-3061T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80162023 | ||||||
| chr5:80162024
|
T | A | 1 | a0001c0001t0001g0121 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.860-3062A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80162024 | ||||||
| chr5:80162185
|
T | C | 1 | a0001c0001t0008g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.860-3223A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80162185 | ||||||
| chr5:80162214
|
C | T | 24 | a0001c0001t0001g0030a0001c0001t0002g0094a0001c0001t0006g0023others(21): Show | 24 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.860-3252G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80162214 | ||||||
| chr5:80162230
|
A | AT | 285 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.860-3269dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80162230 | ||||||
| chr5:80162338
|
A | G | 1 | a0001c0002t0005g0214 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.860-3376T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80162338 | ||||||
| chr5:80162385
|
T | C | 4 | a0001c0001t0008g0259a0001c0001t0030g0255a0001c0001t0030g0257others(1): Show | 4 | HG03130.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.860-3423A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80162385 | ||||||
| chr5:80162397
|
G | A | 1 | a0001c0001t0024g0005 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.860-3435C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80162397 | ||||||
| chr5:80162527
|
C | T | 4 | a0001c0001t0029g0102a0001c0001t0029g0144a0001c0001t0051g0236others(1): Show | 4 | HG02257.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.860-3565G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80162527 | ||||||
| chr5:80162535
|
A | G | 5 | a0001c0001t0013g0067a0001c0001t0013g0068a0001c0002t0022g0272others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.860-3573T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80162535 | ||||||
| chr5:80162542
|
T | C | 26 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0103others(23): Show | 26 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.860-3580A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80162542 | ||||||
| chr5:80162583
|
A | T | 1 | a0001c0001t0033g0060 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.860-3621T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80162583 | ||||||
| chr5:80162640
|
C | T | 33 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0008g0125others(30): Show | 33 | HG00639.hp2 HG01106.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.860-3678G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80162640 | ||||||
| chr5:80162845
|
C | CT | 58 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0103others(55): Show | 58 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.859+3537dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80162845 | ||||||
| chr5:80162857
|
G | A | 1 | a0001c0001t0033g0060 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.859+3526C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80162857 | ||||||
| chr5:80162861
|
C | T | 1 | a0001c0001t0002g0136 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.859+3522G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80162861 | ||||||
| chr5:80163046
|
G | A | 24 | a0001c0001t0001g0030a0001c0001t0002g0094a0001c0001t0006g0023others(21): Show | 24 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.859+3337C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80163046 | ||||||
| chr5:80163078
|
C | G | 2 | a0001c0002t0068g0188a0001c0002t0070g0189 | 2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.859+3305G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80163078 | ||||||
| chr5:80163278
|
C | T | 88 | a0001c0001t0001g0030a0001c0001t0001g0046a0001c0001t0001g0088others(85): Show | 88 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.859+3105G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80163278 | ||||||
| chr5:80163284
|
C | T | 11 | a0001c0001t0008g0240a0001c0001t0020g0057a0001c0001t0029g0144others(8): Show | 11 | HG02451.hp2 HG03041.hp1 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.859+3099G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80163284 | ||||||
| chr5:80163466
|
C | T | 60 | a0001c0001t0001g0030a0001c0001t0002g0094a0001c0001t0002g0277others(57): Show | 60 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.859+2917G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80163466 | ||||||
| chr5:80163546
|
G | GT | 9 | a0001c0001t0001g0107a0001c0001t0008g0259a0001c0001t0030g0255others(6): Show | 9 | HG02083.hp1 HG03130.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.859+2836dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80163546 | ||||||
| chr5:80163546
|
GT | G | 10 | a0001c0001t0001g0268a0001c0001t0009g0126a0001c0001t0009g0139others(7): Show | 10 | HG00735.hp2 HG01167.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.859+2836delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80163546 | ||||||
| chr5:80163606
|
G | GA | 61 | a0001c0001t0001g0030a0001c0001t0002g0094a0001c0001t0002g0277others(58): Show | 61 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.859+2776dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80163606 | ||||||
| chr5:80163612
|
A | T | 1 | a0001c0010t0005g0223 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.859+2771T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80163612 | ||||||
| chr5:80163762
|
C | T | 7 | a0001c0001t0009g0126a0001c0001t0009g0139a0001c0001t0029g0144others(4): Show | 7 | HG02280.hp1 HG03098.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.859+2621G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80163762 | ||||||
| chr5:80163942
|
T | C | 2 | a0001c0001t0006g0064a0002c0003t0009g0228 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.859+2441A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80163942 | ||||||
| chr5:80164018
|
A | G | 1 | a0001c0001t0007g0158 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.859+2365T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80164018 | ||||||
| chr5:80164026
|
T | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0271 | 2 | HG01074.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.859+2357A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80164026 | ||||||
| chr5:80164136
|
T | C | 3 | a0001c0001t0013g0067a0002c0003t0004g0118a0002c0003t0011g0119 | 3 | HG00639.hp2 HG01106.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.859+2247A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80164136 | ||||||
| chr5:80164236
|
T | C | 1 | a0001c0002t0003g0168 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.859+2147A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80164236 | ||||||
| chr5:80164256
|
G | T | 1 | a0001c0001t0065g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.859+2127C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80164256 | ||||||
| chr5:80164324
|
C | T | 3 | a0001c0001t0029g0102a0001c0001t0051g0236a0001c0001t0052g0055 | 3 | HG02257.hp1 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.859+2059G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80164324 | ||||||
| chr5:80164417
|
C | T | 14 | a0001c0001t0001g0194a0001c0001t0001g0271a0001c0001t0008g0240others(11): Show | 14 | HG01074.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.859+1966G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80164417 | ||||||
| chr5:80164577
|
T | G | 1 | a0001c0001t0064g0212 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.859+1806A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80164577 | ||||||
| chr5:80164910
|
G | GT | 14 | a0001c0001t0002g0047a0001c0001t0002g0115a0001c0001t0002g0116others(11): Show | 14 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.859+1472dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80164910 | ||||||
| chr5:80164910
|
G | GTTT | 20 | a0001c0001t0001g0030a0001c0001t0002g0094a0001c0001t0006g0023others(17): Show | 20 | HG00099.hp2 HG00323.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.859+1470_859+1472d others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80164910 | ||||||
| chr5:80164910
|
G | GTTTT | 15 | a0001c0001t0006g0064a0001c0001t0006g0114a0001c0001t0006g0178others(12): Show | 15 | HG00140.hp2 HG00741.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.859+1469_859+1472d others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80164910 | ||||||
| chr5:80164910
|
G | GTTTTT | 9 | a0001c0001t0008g0125a0001c0001t0008g0129a0001c0001t0008g0241others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.859+1468_859+1472d others(7): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80164910 | ||||||
| chr5:80164910
|
GT | G | 147 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(144): Show | 147 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.859+1472delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80164910 | ||||||
| chr5:80164937
|
A | T | 1 | a0001c0001t0065g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.859+1446T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80164937 | ||||||
| chr5:80165002
|
C | T | 2 | a0001c0002t0003g0010a0001c0002t0003g0013 | 2 | NA18984.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.859+1381G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80165002 | ||||||
| chr5:80165200
|
A | T | 2 | a0001c0001t0001g0043a0001c0001t0002g0018 | 2 | HG03688.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.859+1183T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80165200 | ||||||
| chr5:80165287
|
A | G | 60 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0194others(57): Show | 60 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.859+1096T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80165287 | ||||||
| chr5:80165332
|
C | T | 246 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(243): Show | 246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.859+1051G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80165332 | ||||||
| chr5:80165445
|
T | A | 11 | a0001c0001t0001g0039a0001c0001t0001g0225a0001c0001t0001g0269others(8): Show | 11 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.859+938A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80165445 | ||||||
| chr5:80165569
|
G | A | 1 | a0001c0001t0004g0048 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.859+814C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80165569 | ||||||
| chr5:80165604
|
T | C | 36 | a0001c0001t0001g0030a0001c0001t0006g0023a0001c0001t0006g0114others(33): Show | 36 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.859+779A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80165604 | ||||||
| chr5:80165730
|
T | C | 23 | a0001c0001t0001g0039a0001c0001t0001g0194a0001c0001t0001g0225others(20): Show | 23 | HG01074.hp1 HG01243.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.859+653A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80165730 | ||||||
| chr5:80165774
|
A | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0133a0001c0001t0002g0115others(5): Show | 8 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.859+609T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80165774 | ||||||
| chr5:80165818
|
C | T | 2 | a0001c0001t0004g0076a0001c0001t0004g0077 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.859+565G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80165818 | ||||||
| chr5:80165900
|
A | G | 1 | a0001c0001t0009g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.859+483T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80165900 | ||||||
| chr5:80165908
|
A | C | 1 | a0001c0001t0076g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.859+475T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80165908 | ||||||
| chr5:80165979
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0002g0018 | 2 | HG03688.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.859+404A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80165979 | ||||||
| chr5:80166014
|
G | A | 4 | a0001c0001t0008g0259a0001c0001t0030g0255a0001c0001t0030g0257others(1): Show | 4 | HG03130.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.859+369C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80166014 | ||||||
| chr5:80166126
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0002g0018 | 2 | HG03688.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.859+257A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 7/11 | chr5 | 80166126 | ||||||
| chr5:80166587
|
C | T | 1 | a0001c0001t0009g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.764-109G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80166587 | ||||||
| chr5:80166659
|
A | G | 26 | a0001c0001t0001g0030a0001c0001t0006g0023a0001c0001t0006g0114others(23): Show | 26 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.764-181T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80166659 | ||||||
| chr5:80166699
|
T | C | 31 | a0001c0001t0001g0153a0001c0001t0004g0020a0001c0001t0004g0021others(28): Show | 31 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.764-221A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80166699 | ||||||
| chr5:80166741
|
T | A | 1 | a0001c0001t0006g0174 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.764-263A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80166741 | ||||||
| chr5:80167114
|
T | C | 7 | a0001c0001t0008g0259a0001c0001t0009g0208a0001c0001t0030g0255others(4): Show | 7 | HG02451.hp2 HG02647.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.764-636A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80167114 | ||||||
| chr5:80167174
|
G | C | 3 | a0001c0001t0001g0232a0001c0001t0002g0027a0001c0001t0002g0093 | 3 | HG00642.hp1 HG02683.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.764-696C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80167174 | ||||||
| chr5:80167391
|
C | T | 50 | a0001c0001t0001g0030a0001c0001t0001g0177a0001c0001t0006g0023others(47): Show | 50 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.764-913G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80167391 | ||||||
| chr5:80167429
|
C | T | 2 | a0001c0001t0006g0064a0002c0003t0009g0228 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.764-951G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80167429 | ||||||
| chr5:80167521
|
T | C | 6 | a0001c0001t0001g0045a0001c0001t0001g0268a0001c0001t0009g0126others(3): Show | 6 | HG01167.hp2 HG03195.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.764-1043A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80167521 | ||||||
| chr5:80167568
|
T | C | 88 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0177others(85): Show | 88 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.764-1090A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80167568 | ||||||
| chr5:80167603
|
C | T | 2 | a0001c0001t0001g0269a0001c0001t0002g0270 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.764-1125G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80167603 | ||||||
| chr5:80167618
|
T | G | 1 | a0001c0001t0002g0252 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.764-1140A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80167618 | ||||||
| chr5:80168082
|
C | T | 2 | a0001c0001t0033g0060a0001c0001t0044g0149 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.763+1253G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80168082 | ||||||
| chr5:80168126
|
G | A | 2 | a0001c0001t0033g0060a0001c0001t0044g0149 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.763+1209C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80168126 | ||||||
| chr5:80168215
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.763+1120C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80168215 | ||||||
| chr5:80168288
|
G | A | 1 | a0001c0002t0022g0272 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.763+1047C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80168288 | ||||||
| chr5:80168321
|
C | T | 39 | a0001c0001t0001g0153a0001c0001t0002g0094a0001c0001t0004g0073others(36): Show | 39 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.763+1014G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80168321 | ||||||
| chr5:80168374
|
A | T | 1 | a0001c0001t0001g0170 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.763+961T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80168374 | ||||||
| chr5:80168439
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0004g0247 | 2 | HG02015.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.763+896C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80168439 | ||||||
| chr5:80168453
|
A | G | 91 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0177others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.763+882T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80168453 | ||||||
| chr5:80168492
|
C | T | 2 | a0001c0001t0020g0057a0001c0001t0041g0279 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.763+843G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80168492 | ||||||
| chr5:80168564
|
G | A | 26 | a0001c0001t0001g0177a0001c0001t0008g0125a0001c0001t0008g0129others(23): Show | 26 | HG00323.hp1 HG00609.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.763+771C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80168564 | ||||||
| chr5:80168678
|
C | A | 1 | a0001c0001t0001g0170 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.763+657G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80168678 | ||||||
| chr5:80168713
|
G | A | 28 | a0001c0001t0001g0177a0001c0001t0008g0125a0001c0001t0008g0129others(25): Show | 28 | HG00323.hp1 HG00609.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.763+622C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80168713 | ||||||
| chr5:80168789
|
C | G | 3 | a0001c0001t0002g0134a0001c0001t0002g0211a0001c0001t0002g0237 | 3 | HG00733.hp1 HG01168.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.763+546G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80168789 | ||||||
| chr5:80168863
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.763+472G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80168863 | ||||||
| chr5:80168909
|
A | C | 2 | a0001c0001t0020g0057a0001c0001t0041g0279 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.763+426T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80168909 | ||||||
| chr5:80169115
|
G | A | 3 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0181 | 3 | NA18977.hp2 NA19009.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.763+220C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80169115 | ||||||
| chr5:80169143
|
C | T | 4 | a0001c0001t0038g0111a0001c0001t0055g0276a0001c0006t0020g0127others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+192G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80169143 | ||||||
| chr5:80169274
|
G | T | 2 | a0001c0001t0011g0123a0001c0001t0011g0245 | 2 | HG01106.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.763+61C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80169274 | ||||||
| chr5:80169309
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0004g0247 | 2 | HG02015.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.763+26G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 6/11 | chr5 | 80169309 | ||||||
| chr5:80169576
|
G | A | 1 | a0001c0001t0013g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.552-30C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80169576 | ||||||
| chr5:80169596
|
C | A | 4 | a0001c0001t0029g0102a0001c0001t0029g0144a0001c0001t0051g0236others(1): Show | 4 | HG02257.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.552-50G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80169596 | ||||||
| chr5:80169692
|
T | C | 2 | a0001c0001t0046g0260a0001c0001t0047g0261 | 2 | HG01167.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.552-146A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80169692 | ||||||
| chr5:80169748
|
C | T | 1 | a0001c0001t0055g0276 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.552-202G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80169748 | ||||||
| chr5:80169838
|
C | G | 2 | a0001c0001t0046g0260a0001c0001t0047g0261 | 2 | HG01167.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.552-292G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80169838 | ||||||
| chr5:80169840
|
A | C | 1 | a0001c0001t0002g0018 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.552-294T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80169840 | ||||||
| chr5:80169920
|
C | T | 2 | a0001c0001t0009g0126a0001c0001t0075g0284 | 2 | HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.552-374G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80169920 | ||||||
| chr5:80169945
|
T | C | 2 | a0001c0001t0020g0057a0001c0001t0041g0279 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.552-399A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80169945 | ||||||
| chr5:80170025
|
A | C | 4 | a0001c0001t0008g0125a0001c0001t0008g0129a0001c0001t0008g0241others(1): Show | 4 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.552-479T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80170025 | ||||||
| chr5:80170041
|
G | A | 1 | a0001c0001t0065g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.552-495C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80170041 | ||||||
| chr5:80170086
|
A | T | 1 | a0001c0001t0065g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.552-540T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80170086 | ||||||
| chr5:80170113
|
A | G | 2 | a0001c0001t0013g0067a0001c0002t0022g0272 | 2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.552-567T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80170113 | ||||||
| chr5:80170136
|
T | G | 1 | a0001c0001t0001g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.552-590A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80170136 | ||||||
| chr5:80170344
|
A | C | 1 | a0001c0001t0001g0213 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.552-798T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80170344 | ||||||
| chr5:80170380
|
C | T | 90 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0177others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.552-834G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80170380 | ||||||
| chr5:80170386
|
G | T | 2 | a0001c0001t0009g0126a0001c0001t0075g0284 | 2 | HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.552-840C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80170386 | ||||||
| chr5:80171141
|
C | T | 2 | a0001c0002t0068g0188a0001c0002t0070g0189 | 2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.552-1595G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80171141 | ||||||
| chr5:80171357
|
T | C | 7 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0013g0068others(4): Show | 7 | HG01243.hp2 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.552-1811A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80171357 | ||||||
| chr5:80171379
|
A | G | 1 | a0001c0001t0011g0245 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.552-1833T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80171379 | ||||||
| chr5:80171526
|
A | T | 2 | a0001c0001t0013g0067a0001c0002t0022g0272 | 2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.552-1980T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80171526 | ||||||
| chr5:80171536
|
A | C | 4 | a0001c0001t0001g0153a0001c0001t0004g0247a0001c0001t0004g0282others(1): Show | 4 | HG01943.hp2 HG01975.hp2 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.552-1990T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80171536 | ||||||
| chr5:80171608
|
T | C | 1 | a0001c0006t0020g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.552-2062A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80171608 | ||||||
| chr5:80171612
|
T | C | 1 | a0001c0002t0003g0193 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.552-2066A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80171612 | ||||||
| chr5:80171669
|
C | G | 1 | a0001c0001t0001g0029 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.552-2123G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80171669 | ||||||
| chr5:80171724
|
C | CA | 3 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0002g0252 | 3 | NA18952.hp1 NA19003.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.552-2179dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80171724 | ||||||
| chr5:80171895
|
C | A | 29 | a0001c0001t0001g0039a0001c0001t0001g0225a0001c0001t0001g0269others(26): Show | 29 | HG01167.hp2 HG01243.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.552-2349G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80171895 | ||||||
| chr5:80171980
|
A | T | 2 | a0001c0001t0009g0126a0001c0001t0075g0284 | 2 | HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.552-2434T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80171980 | ||||||
| chr5:80172032
|
A | C | 1 | a0001c0001t0015g0258 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.552-2486T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80172032 | ||||||
| chr5:80172036
|
C | T | 4 | a0001c0001t0029g0102a0001c0001t0029g0144a0001c0001t0051g0236others(1): Show | 4 | HG02257.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.552-2490G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80172036 | ||||||
| chr5:80172074
|
G | A | 31 | a0001c0001t0001g0177a0001c0001t0001g0194a0001c0001t0001g0271others(28): Show | 31 | HG00323.hp1 HG00609.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.552-2528C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80172074 | ||||||
| chr5:80172083
|
G | A | 1 | a0001c0001t0065g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.552-2537C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80172083 | ||||||
| chr5:80172162
|
T | C | 1 | a0001c0001t0002g0237 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.552-2616A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80172162 | ||||||
| chr5:80172186
|
C | T | 1 | a0001c0001t0034g0207 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.552-2640G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80172186 | ||||||
| chr5:80172225
|
G | C | 2 | a0001c0001t0013g0067a0001c0002t0022g0272 | 2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.552-2679C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80172225 | ||||||
| chr5:80172262
|
G | A | 2 | a0001c0001t0009g0126a0001c0001t0075g0284 | 2 | HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.551+2692C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80172262 | ||||||
| chr5:80172412
|
T | C | 5 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0040g0066others(2): Show | 5 | HG01243.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.551+2542A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80172412 | ||||||
| chr5:80172593
|
AATGATAA others(51): Show |
A | 4 | a0001c0001t0029g0102a0001c0001t0029g0144a0001c0001t0051g0236others(1): Show | 4 | HG02257.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.551+2303_551+2360d others(60): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80172593 | ||||||
| chr5:80172603
|
A | G | 2 | a0001c0001t0046g0260a0001c0001t0047g0261 | 2 | HG01167.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.551+2351T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80172603 | ||||||
| chr5:80172794
|
G | C | 44 | a0001c0001t0001g0153a0001c0001t0001g0177a0001c0001t0002g0094others(41): Show | 44 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.551+2160C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80172794 | ||||||
| chr5:80172798
|
G | A | 1 | a0001c0001t0065g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.551+2156C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80172798 | ||||||
| chr5:80172956
|
C | G | 1 | a0001c0002t0031g0001 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.551+1998G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80172956 | ||||||
| chr5:80172978
|
T | C | 7 | a0001c0001t0038g0111a0001c0001t0046g0260a0001c0001t0047g0261others(4): Show | 7 | HG01167.hp2 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.551+1976A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80172978 | ||||||
| chr5:80173225
|
A | AGAAG | 18 | a0001c0001t0001g0092a0001c0001t0002g0024a0001c0001t0002g0093others(15): Show | 18 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.551+1725_551+1728d others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173225 | ||||||
| chr5:80173225
|
A | AGAAGGAA others(1): Show |
9 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0151others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.551+1721_551+1728d others(10): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173225 | ||||||
| chr5:80173225
|
AGAAG | A | 108 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0043others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.551+1725_551+1728d others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173225 | ||||||
| chr5:80173225
|
AGAAGGAA others(1): Show |
A | 46 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0177others(43): Show | 46 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.551+1721_551+1728d others(10): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173225 | ||||||
| chr5:80173225
|
AGAAGGAA others(5): Show |
A | 25 | a0001c0001t0001g0133a0001c0001t0001g0190a0001c0001t0001g0194others(22): Show | 25 | HG00639.hp1 HG00735.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.551+1717_551+1728d others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173225 | ||||||
| chr5:80173225
|
AGAAGGAA others(9): Show |
A | 5 | a0001c0001t0002g0277a0001c0001t0007g0150a0001c0001t0040g0066others(2): Show | 5 | HG01243.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.551+1713_551+1728d others(18): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173225 | ||||||
| chr5:80173225
|
AGAAGGAA others(13): Show |
A | 11 | a0001c0001t0001g0039a0001c0001t0001g0225a0001c0001t0001g0269others(8): Show | 11 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.551+1709_551+1728d others(22): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173225 | ||||||
| chr5:80173255
|
A | G | 6 | a0001c0001t0001g0194a0001c0001t0001g0271a0001c0001t0010g0062others(3): Show | 6 | HG00735.hp2 HG01074.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.551+1699T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173255 | ||||||
| chr5:80173282
|
AAAATG | A | 6 | a0001c0001t0001g0121a0001c0001t0001g0200a0001c0001t0014g0019others(3): Show | 6 | HG02257.hp1 NA18955.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.551+1667_551+1671d others(7): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173282 | ||||||
| chr5:80173528
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.551+1426C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173528 | ||||||
| chr5:80173542
|
G | C | 1 | a0001c0001t0013g0068 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.551+1412C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173542 | ||||||
| chr5:80173544
|
C | A | 1 | a0001c0001t0001g0190 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.551+1410G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173544 | ||||||
| chr5:80173563
|
T | A | 1 | a0001c0001t0013g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.551+1391A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173563 | ||||||
| chr5:80173595
|
C | CAAAAG | 24 | a0001c0001t0001g0015a0001c0001t0001g0030a0001c0001t0001g0213others(21): Show | 24 | HG00323.hp2 HG00733.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.551+1354_551+1358d others(7): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173595 | ||||||
| chr5:80173595
|
C | CAAAAGAA others(3): Show |
1 | a0001c0001t0006g0023 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.551+1349_551+1358d others(12): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173595 | ||||||
| chr5:80173706
|
A | G | 64 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0213others(61): Show | 64 | HG00099.hp2 HG00323.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.551+1248T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173706 | ||||||
| chr5:80173725
|
C | T | 33 | a0001c0001t0001g0043a0001c0001t0001g0194a0001c0001t0001g0271others(30): Show | 33 | HG00140.hp2 HG00735.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.551+1229G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173725 | ||||||
| chr5:80173758
|
C | T | 4 | a0001c0001t0029g0102a0001c0001t0029g0144a0001c0001t0051g0236others(1): Show | 4 | HG02257.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.551+1196G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173758 | ||||||
| chr5:80173816
|
C | G | 34 | a0001c0001t0001g0043a0001c0001t0001g0194a0001c0001t0001g0271others(31): Show | 34 | HG00140.hp2 HG00735.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.551+1138G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173816 | ||||||
| chr5:80173825
|
C | A | 2 | a0001c0001t0009g0208a0001c0001t0048g0143 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.551+1129G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173825 | ||||||
| chr5:80173946
|
CTG | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0121a0001c0001t0014g0086 | 3 | HG00438.hp2 NA18990.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.551+1006_551+1007d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173946 | ||||||
| chr5:80173954
|
CACAAAAT others(7): Show |
C | 2 | a0001c0001t0002g0044a0001c0001t0002g0120 | 2 | HG00099.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.551+986_551+999del others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80173954 | ||||||
| chr5:80174067
|
A | G | 109 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0043others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.551+887T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174067 | ||||||
| chr5:80174168
|
C | A | 1 | a0001c0001t0001g0268 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.551+786G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174168 | ||||||
| chr5:80174188
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.551+766G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174188 | ||||||
| chr5:80174208
|
A | G | 34 | a0001c0001t0001g0043a0001c0001t0001g0194a0001c0001t0001g0271others(31): Show | 34 | HG00140.hp2 HG00735.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.551+746T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174208 | ||||||
| chr5:80174294
|
G | C | 2 | a0002c0004t0005g0110a0002c0004t0016g0231 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.551+660C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174294 | ||||||
| chr5:80174337
|
G | A | 35 | a0001c0001t0001g0043a0001c0001t0001g0194a0001c0001t0001g0271others(32): Show | 35 | HG00140.hp2 HG00735.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.551+617C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174337 | ||||||
| chr5:80174369
|
A | AAAT | 7 | a0001c0001t0002g0027a0001c0001t0007g0142a0001c0001t0009g0139others(4): Show | 7 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.551+582_551+584dup others(3): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174369 | ||||||
| chr5:80174369
|
A | AAATAAT | 27 | a0001c0001t0001g0232a0001c0001t0004g0247a0001c0001t0004g0282others(24): Show | 27 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.551+579_551+584dup others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174369 | ||||||
| chr5:80174369
|
A | AAATAATA others(2): Show |
43 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(40): Show | 43 | HG00621.hp2 HG00639.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.551+576_551+584dup others(9): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174369 | ||||||
| chr5:80174369
|
A | AAATAATA others(5): Show |
59 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.551+573_551+584dup others(12): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174369 | ||||||
| chr5:80174369
|
A | AAATAATA others(8): Show |
42 | a0001c0001t0001g0107a0001c0001t0001g0121a0001c0001t0001g0153others(39): Show | 42 | HG00323.hp1 HG00621.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.551+570_551+584dup others(15): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174369 | ||||||
| chr5:80174369
|
A | AAATAATA others(11): Show |
23 | a0001c0001t0001g0029a0001c0001t0001g0045a0001c0001t0001g0089others(20): Show | 23 | HG00438.hp2 HG00741.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.551+567_551+584dup others(18): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174369 | ||||||
| chr5:80174369
|
A | AAATAATA others(14): Show |
5 | a0001c0001t0001g0103a0001c0001t0001g0162a0001c0002t0003g0035others(2): Show | 5 | HG02129.hp1 NA18948.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.551+564_551+584dup others(21): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174369 | ||||||
| chr5:80174369
|
A | AAATAATA others(17): Show |
1 | a0001c0002t0003g0032 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.551+561_551+584dup others(24): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174369 | ||||||
| chr5:80174369
|
A | AATAATAA others(4): Show |
1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.551+584_551+585ins others(11): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174369 | ||||||
| chr5:80174369
|
AAAT | A | 37 | a0001c0001t0001g0043a0001c0001t0001g0194a0001c0001t0001g0271others(34): Show | 37 | HG00140.hp2 HG00735.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.551+582_551+584del others(3): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174369 | ||||||
| chr5:80174369
|
AAATAAT | A | 6 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0150others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.551+579_551+584del others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174369 | ||||||
| chr5:80174399
|
T | TAATAATA others(7): Show |
1 | a0001c0001t0002g0219 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.551+554_551+555ins others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174399 | ||||||
| chr5:80174404
|
A | ATAATAAT others(3): Show |
16 | a0001c0001t0001g0030a0001c0001t0001g0213a0001c0001t0006g0023others(13): Show | 16 | HG00099.hp2 HG00323.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.551+549_551+550ins others(10): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174404 | ||||||
| chr5:80174404
|
A | ATAATAAT others(6): Show |
4 | a0001c0001t0002g0157a0001c0001t0002g0248a0001c0001t0055g0276others(1): Show | 4 | HG02135.hp1 HG02135.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.551+549_551+550ins others(13): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174404 | ||||||
| chr5:80174404
|
A | ATAATAAT others(9): Show |
3 | a0001c0001t0009g0226a0001c0002t0068g0188a0001c0002t0070g0189 | 3 | HG03688.hp1 HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.551+549_551+550ins others(16): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174404 | ||||||
| chr5:80174405
|
A | T | 1 | a0001c0001t0002g0219 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.551+549T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174405 | ||||||
| chr5:80174407
|
G | T | 24 | a0001c0001t0001g0030a0001c0001t0001g0213a0001c0001t0006g0023others(21): Show | 24 | HG00099.hp2 HG00323.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.551+547C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174407 | ||||||
| chr5:80174425
|
G | T | 67 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0213others(64): Show | 67 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.551+529C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174425 | ||||||
| chr5:80174451
|
C | T | 3 | a0001c0001t0036g0254a0001c0006t0020g0127a0001c0006t0045g0128 | 3 | HG02451.hp2 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.551+503G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174451 | ||||||
| chr5:80174488
|
T | A | 7 | a0001c0001t0002g0278a0001c0001t0015g0063a0001c0001t0015g0256others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.551+466A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174488 | ||||||
| chr5:80174543
|
A | G | 1 | a0001c0001t0062g0283 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.551+411T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174543 | ||||||
| chr5:80174682
|
T | C | 1 | a0001c0002t0005g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.551+272A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 5/11 | chr5 | 80174682 | ||||||
| chr5:80175166
|
CCATATAA others(19): Show |
C | 1 | a0001c0001t0002g0248 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.458-145_458-120del others(26): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80175166 | ||||||
| chr5:80175319
|
TC | T | 3 | a0001c0001t0020g0057a0001c0001t0059g0059a0001c0002t0005g0058 | 3 | HG01243.hp1 HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.458-273delG | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80175319 | ||||||
| chr5:80175351
|
T | A | 2 | a0002c0005t0019g0042a0002c0005t0019g0273 | 2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.458-304A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80175351 | ||||||
| chr5:80175523
|
G | A | 82 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(79): Show | 82 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.458-476C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80175523 | ||||||
| chr5:80175560
|
A | G | 253 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(250): Show | 253 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.458-513T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80175560 | ||||||
| chr5:80175652
|
T | G | 1 | a0001c0001t0076g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.458-605A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80175652 | ||||||
| chr5:80175677
|
T | C | 1 | a0001c0001t0010g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.458-630A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80175677 | ||||||
| chr5:80175717
|
C | T | 59 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0213others(56): Show | 59 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.458-670G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80175717 | ||||||
| chr5:80175863
|
C | CA | 10 | a0001c0001t0001g0162a0001c0001t0001g0268a0001c0001t0002g0018others(7): Show | 10 | HG02027.hp2 HG02129.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.458-817dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80175863 | ||||||
| chr5:80175876
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0002g0120 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.458-839_458-830del others(10): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80175876 | ||||||
| chr5:80175882
|
AAAAG | A | 6 | a0001c0001t0008g0125a0001c0001t0008g0129a0001c0001t0008g0241others(3): Show | 6 | HG01891.hp1 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-839_458-836del others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80175882 | ||||||
| chr5:80175883
|
AAAG | A | 33 | a0001c0001t0002g0277a0001c0001t0002g0278a0001c0001t0007g0069others(30): Show | 33 | HG01109.hp1 HG01167.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.458-839_458-837del others(3): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80175883 | ||||||
| chr5:80175884
|
AAG | A | 70 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0028others(67): Show | 70 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.458-839_458-838del others(2): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80175884 | ||||||
| chr5:80175885
|
AG | A | 33 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0030others(30): Show | 33 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.458-839delC | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80175885 | ||||||
| chr5:80175886
|
G | A | 141 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0043others(138): Show | 141 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.458-839C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80175886 | ||||||
| chr5:80176056
|
A | G | 139 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(136): Show | 139 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.458-1009T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80176056 | ||||||
| chr5:80176066
|
C | A | 6 | a0001c0002t0003g0032a0001c0002t0003g0035a0001c0002t0003g0036others(3): Show | 6 | NA18942.hp2 NA18963.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.458-1019G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80176066 | ||||||
| chr5:80176125
|
G | A | 1 | a0001c0001t0002g0252 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.458-1078C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80176125 | ||||||
| chr5:80176128
|
G | A | 12 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0150others(9): Show | 12 | HG01167.hp2 HG01243.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.458-1081C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80176128 | ||||||
| chr5:80176185
|
G | A | 2 | a0001c0001t0037g0262a0001c0001t0043g0234 | 2 | HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.457+1130C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80176185 | ||||||
| chr5:80176307
|
G | A | 140 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(137): Show | 140 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.457+1008C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80176307 | ||||||
| chr5:80176527
|
G | T | 1 | a0001c0001t0002g0027 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.457+788C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80176527 | ||||||
| chr5:80176576
|
CA | C | 3 | a0001c0001t0051g0236a0001c0001t0052g0055a0001c0002t0031g0001 | 3 | HG02257.hp1 HG03471.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.457+738delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80176576 | ||||||
| chr5:80176712
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.457+603G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80176712 | ||||||
| chr5:80176800
|
C | A | 1 | a0001c0001t0008g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.457+515G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80176800 | ||||||
| chr5:80176891
|
A | G | 142 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(139): Show | 142 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.457+424T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80176891 | ||||||
| chr5:80176904
|
A | G | 2 | a0001c0001t0038g0111a0001c0001t0055g0276 | 2 | HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.457+411T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80176904 | ||||||
| chr5:80176939
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.457+376G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80176939 | ||||||
| chr5:80176940
|
G | A | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.457+375C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80176940 | ||||||
| chr5:80177032
|
C | A | 2 | a0002c0005t0019g0042a0002c0005t0019g0273 | 2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.457+283G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80177032 | ||||||
| chr5:80177065
|
G | A | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.457+250C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80177065 | ||||||
| chr5:80177112
|
G | A | 1 | a0001c0001t0021g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.457+203C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80177112 | ||||||
| chr5:80177124
|
G | A | 1 | a0001c0002t0022g0272 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.457+191C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80177124 | ||||||
| chr5:80177260
|
T | A | 5 | a0001c0001t0036g0254a0001c0001t0038g0111a0001c0001t0055g0276others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.457+55A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80177260 | ||||||
| chr5:80177294
|
C | G | 1 | a0001c0009t0035g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.457+21G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 4/11 | chr5 | 80177294 | ||||||
| chr5:80177464
|
G | T | 73 | a0001c0001t0001g0030a0001c0001t0001g0213a0001c0001t0002g0277others(70): Show | 73 | HG00639.hp2 HG00733.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.375-67C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 3/11 | chr5 | 80177464 | ||||||
| chr5:80177488
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.375-91T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 3/11 | chr5 | 80177488 | ||||||
| chr5:80177683
|
C | A | 10 | a0001c0001t0001g0268a0001c0001t0008g0125a0001c0001t0008g0241others(7): Show | 10 | HG01496.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.374+203G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 3/11 | chr5 | 80177683 | ||||||
| chr5:80177755
|
C | T | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.374+131G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 3/11 | chr5 | 80177755 | ||||||
| chr5:80177835
|
C | T | 1 | a0001c0001t0009g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.374+51G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 3/11 | chr5 | 80177835 | ||||||
| chr5:80177852
|
A | G | 4 | a0001c0001t0002g0109a0001c0001t0002g0280a0001c0001t0007g0281others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.374+34T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 3/11 | chr5 | 80177852 | ||||||
| chr5:80178128
|
G | A | 3 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0004g0233 | 3 | HG01099.hp2 HG01256.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196-64C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178128 | ||||||
| chr5:80178155
|
T | C | 3 | a0001c0001t0008g0129a0001c0001t0008g0240a0001c0001t0058g0243 | 3 | HG02647.hp2 HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.196-91A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178155 | ||||||
| chr5:80178329
|
CT | C | 5 | a0001c0001t0009g0139a0001c0001t0051g0236a0001c0001t0052g0055others(2): Show | 5 | HG02257.hp1 HG02280.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-266delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178329 | ||||||
| chr5:80178366
|
C | G | 127 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0045others(124): Show | 127 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.196-302G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178366 | ||||||
| chr5:80178381
|
C | G | 121 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0043others(118): Show | 121 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.196-317G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178381 | ||||||
| chr5:80178495
|
T | C | 199 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(196): Show | 199 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.196-431A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178495 | ||||||
| chr5:80178496
|
G | A | 194 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(191): Show | 194 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.196-432C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178496 | ||||||
| chr5:80178519
|
T | C | 2 | a0002c0004t0005g0110a0002c0004t0016g0231 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.196-455A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178519 | ||||||
| chr5:80178537
|
A | AT | 65 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(62): Show | 65 | HG00408.hp1 HG00438.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.196-474dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178537 | ||||||
| chr5:80178537
|
A | ATT | 12 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0002g0024others(9): Show | 12 | HG00099.hp2 HG01099.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.196-475_196-474dup others(2): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178537 | ||||||
| chr5:80178537
|
A | T | 5 | a0001c0001t0009g0126a0001c0001t0034g0207a0001c0001t0041g0279others(2): Show | 5 | HG01884.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-473T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178537 | ||||||
| chr5:80178537
|
AT | A | 58 | a0001c0001t0001g0015a0001c0001t0001g0030a0001c0001t0001g0039others(55): Show | 58 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.196-474delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178537 | ||||||
| chr5:80178537
|
ATT | A | 6 | a0001c0001t0007g0249a0001c0001t0010g0062a0001c0001t0048g0143others(3): Show | 6 | HG00140.hp1 HG02257.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-475_196-474del others(2): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178537 | ||||||
| chr5:80178537
|
ATTT | A | 9 | a0001c0001t0009g0139a0001c0001t0009g0208a0001c0001t0036g0254others(6): Show | 9 | HG02280.hp1 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.196-476_196-474del others(3): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178537 | ||||||
| chr5:80178537
|
ATTTT | A | 13 | a0001c0001t0002g0101a0001c0001t0002g0109a0001c0001t0008g0259others(10): Show | 13 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.196-477_196-474del others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178537 | ||||||
| chr5:80178537
|
ATTTTT | A | 95 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0045others(92): Show | 95 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.196-478_196-474del others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178537 | ||||||
| chr5:80178562
|
T | G | 1 | a0001c0001t0054g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.196-498A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178562 | ||||||
| chr5:80178653
|
C | T | 204 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(201): Show | 204 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.196-589G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178653 | ||||||
| chr5:80178753
|
G | C | 1 | a0001c0001t0043g0234 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.196-689C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178753 | ||||||
| chr5:80178808
|
A | AT | 285 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.196-745dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178808 | ||||||
| chr5:80178815
|
G | A | 5 | a0001c0001t0036g0254a0001c0001t0038g0111a0001c0001t0055g0276others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-751C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178815 | ||||||
| chr5:80178861
|
A | G | 1 | a0001c0001t0043g0234 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.196-797T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178861 | ||||||
| chr5:80178872
|
ACACT | A | 3 | a0001c0001t0013g0140a0001c0001t0046g0260a0001c0001t0047g0261 | 3 | HG01167.hp2 HG03486.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.196-812_196-809del others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178872 | ||||||
| chr5:80178933
|
A | G | 2 | a0001c0001t0029g0102a0001c0001t0029g0144 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.196-869T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178933 | ||||||
| chr5:80178992
|
A | AT | 66 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(63): Show | 66 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.196-929dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80178992 | ||||||
| chr5:80179014
|
G | A | 46 | a0001c0001t0001g0014a0001c0001t0001g0089a0001c0001t0001g0170others(43): Show | 46 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.196-950C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80179014 | ||||||
| chr5:80179157
|
G | A | 4 | a0001c0001t0004g0247a0001c0001t0004g0282a0001c0001t0062g0283others(1): Show | 4 | HG01943.hp2 HG01975.hp2 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-1093C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80179157 | ||||||
| chr5:80179196
|
G | A | 1 | a0001c0001t0010g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.196-1132C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80179196 | ||||||
| chr5:80179202
|
G | A | 16 | a0001c0001t0006g0114a0001c0001t0006g0167a0001c0001t0006g0173others(13): Show | 16 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.196-1138C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80179202 | ||||||
| chr5:80179248
|
G | A | 39 | a0001c0001t0001g0216a0001c0001t0001g0268a0001c0001t0006g0174others(36): Show | 39 | HG00323.hp2 HG00639.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.196-1184C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80179248 | ||||||
| chr5:80179252
|
T | C | 2 | a0002c0003t0004g0118a0002c0003t0011g0119 | 2 | HG00639.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.196-1188A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80179252 | ||||||
| chr5:80179268
|
T | C | 29 | a0001c0001t0001g0216a0001c0001t0006g0174a0001c0001t0008g0240others(26): Show | 29 | HG00323.hp2 HG00639.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.196-1204A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80179268 | ||||||
| chr5:80179331
|
T | C | 68 | a0001c0001t0001g0039a0001c0001t0001g0216a0001c0001t0001g0225others(65): Show | 68 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.196-1267A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80179331 | ||||||
| chr5:80179444
|
T | G | 68 | a0001c0001t0001g0015a0001c0001t0001g0039a0001c0001t0001g0133others(65): Show | 68 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.196-1380A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80179444 | ||||||
| chr5:80179467
|
A | C | 1 | a0001c0002t0003g0090 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.196-1403T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80179467 | ||||||
| chr5:80179647
|
G | C | 2 | a0001c0001t0051g0236a0001c0001t0052g0055 | 2 | HG02257.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.196-1583C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80179647 | ||||||
| chr5:80179709
|
T | C | 12 | a0001c0001t0001g0015a0001c0001t0001g0133a0001c0001t0002g0115others(9): Show | 12 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.196-1645A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80179709 | ||||||
| chr5:80179837
|
T | C | 2 | a0002c0005t0019g0042a0002c0005t0019g0273 | 2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.196-1773A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80179837 | ||||||
| chr5:80180138
|
A | G | 5 | a0001c0001t0008g0259a0001c0001t0010g0062a0001c0001t0013g0067others(2): Show | 5 | HG03209.hp1 HG03225.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-2074T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80180138 | ||||||
| chr5:80180191
|
A | T | 4 | a0001c0001t0010g0235a0001c0001t0055g0276a0001c0002t0027g0148others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-2127T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80180191 | ||||||
| chr5:80180278
|
A | G | 10 | a0001c0001t0007g0069a0001c0001t0007g0158a0001c0001t0007g0275others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-2214T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80180278 | ||||||
| chr5:80180306
|
A | C | 2 | a0001c0002t0003g0078a0001c0002t0003g0081 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.196-2242T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80180306 | ||||||
| chr5:80180418
|
C | T | 3 | a0001c0001t0013g0140a0001c0001t0046g0260a0001c0001t0047g0261 | 3 | HG01167.hp2 HG03486.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.196-2354G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80180418 | ||||||
| chr5:80180511
|
T | C | 1 | a0001c0001t0004g0138 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.196-2447A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80180511 | ||||||
| chr5:80180588
|
C | A | 71 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(68): Show | 71 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.196-2524G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80180588 | ||||||
| chr5:80180588
|
C | T | 1 | a0001c0001t0007g0158 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.196-2524G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80180588 | ||||||
| chr5:80180589
|
G | A | 2 | a0002c0005t0019g0042a0002c0005t0019g0273 | 2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.196-2525C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80180589 | ||||||
| chr5:80180750
|
G | T | 3 | a0001c0001t0036g0254a0001c0006t0020g0127a0001c0006t0045g0128 | 3 | HG02451.hp2 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.196-2686C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80180750 | ||||||
| chr5:80180850
|
T | C | 1 | a0001c0001t0065g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.196-2786A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80180850 | ||||||
| chr5:80180882
|
C | T | 4 | a0001c0001t0029g0102a0001c0001t0029g0144a0002c0004t0005g0110others(1): Show | 4 | HG02965.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-2818G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80180882 | ||||||
| chr5:80180915
|
T | G | 76 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(73): Show | 76 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.196-2851A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80180915 | ||||||
| chr5:80180977
|
C | A | 14 | a0001c0001t0001g0015a0001c0001t0001g0133a0001c0001t0002g0115others(11): Show | 14 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.196-2913G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80180977 | ||||||
| chr5:80181019
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.196-2955C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181019 | ||||||
| chr5:80181028
|
G | C | 126 | a0001c0001t0001g0015a0001c0001t0001g0039a0001c0001t0001g0043others(123): Show | 126 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.196-2964C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181028 | ||||||
| chr5:80181045
|
C | T | 1 | a0002c0003t0009g0228 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.196-2981G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181045 | ||||||
| chr5:80181146
|
C | T | 1 | a0001c0002t0031g0001 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.196-3082G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181146 | ||||||
| chr5:80181329
|
C | A | 6 | a0001c0001t0036g0254a0001c0001t0041g0279a0001c0001t0075g0284others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-3265G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181329 | ||||||
| chr5:80181390
|
G | A | 1 | a0001c0001t0013g0140 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.196-3326C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181390 | ||||||
| chr5:80181414
|
T | TATTGTGT others(13): Show |
2 | a0001c0001t0001g0006a0001c0001t0024g0005 | 2 | HG01943.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.196-3351_196-3350i others(22): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181414 | ||||||
| chr5:80181414
|
T | TATTGTGT others(15): Show |
9 | a0001c0001t0001g0166a0001c0001t0002g0027a0001c0001t0002g0071others(6): Show | 9 | HG02145.hp2 HG02683.hp1 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.196-3351_196-3350i others(24): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181414 | ||||||
| chr5:80181414
|
T | TATTGTGT others(17): Show |
16 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0028others(13): Show | 16 | HG00099.hp2 HG01168.hp1 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.196-3351_196-3350i others(26): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181414 | ||||||
| chr5:80181414
|
T | TATTGTGT others(19): Show |
11 | a0001c0001t0001g0100a0001c0001t0001g0190a0001c0001t0001g0195others(8): Show | 11 | HG00438.hp2 HG00642.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-3351_196-3350i others(28): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181414 | ||||||
| chr5:80181414
|
T | TATTGTGT others(21): Show |
18 | a0001c0001t0001g0046a0001c0001t0001g0107a0001c0001t0001g0181others(15): Show | 18 | HG00408.hp1 HG01169.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.196-3351_196-3350i others(30): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181414 | ||||||
| chr5:80181414
|
T | TATTGTGT others(23): Show |
10 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0002g0024others(7): Show | 10 | HG01099.hp1 HG01978.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-3351_196-3350i others(32): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181414 | ||||||
| chr5:80181414
|
T | TATTGTGT others(25): Show |
4 | a0001c0001t0002g0025a0001c0001t0002g0239a0001c0002t0003g0035others(1): Show | 4 | HG01433.hp2 HG01993.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-3351_196-3350i others(34): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181414 | ||||||
| chr5:80181414
|
T | TATTGTGT others(27): Show |
1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.196-3351_196-3350i others(36): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181414 | ||||||
| chr5:80181414
|
T | TATTGTGT others(29): Show |
2 | a0001c0002t0071g0037a0001c0010t0005g0223 | 2 | HG04199.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.196-3351_196-3350i others(38): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181414 | ||||||
| chr5:80181414
|
T | TATTGTGT others(35): Show |
1 | a0001c0001t0001g0007 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.196-3351_196-3350i others(44): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181414 | ||||||
| chr5:80181416
|
T | G | 75 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(72): Show | 75 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.196-3352A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181416 | ||||||
| chr5:80181416
|
T | TTG | 5 | a0001c0001t0002g0237a0001c0001t0004g0049a0001c0001t0037g0262others(2): Show | 5 | HG00733.hp1 HG03139.hp2 NA20129.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-3354_196-3353d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181416 | ||||||
| chr5:80181416
|
T | TTGTG | 88 | a0001c0001t0001g0043a0001c0001t0001g0089a0001c0001t0001g0194others(85): Show | 88 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.196-3356_196-3353d others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181416 | ||||||
| chr5:80181416
|
T | TTGTGTG | 17 | a0001c0001t0001g0015a0001c0001t0001g0039a0001c0001t0002g0134others(14): Show | 17 | HG00741.hp2 HG01070.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.196-3358_196-3353d others(8): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181416 | ||||||
| chr5:80181416
|
T | TTGTGTGT others(1): Show |
8 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0006g0064others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-3360_196-3353d others(10): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181416 | ||||||
| chr5:80181416
|
T | TTGTGTGT others(3): Show |
3 | a0001c0001t0042g0065a0001c0001t0044g0149a0001c0001t0050g0265 | 3 | HG02818.hp2 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.196-3362_196-3353d others(12): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181416 | ||||||
| chr5:80181416
|
T | TTGTGTGT others(5): Show |
1 | a0001c0001t0013g0068 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.196-3364_196-3353d others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181416 | ||||||
| chr5:80181416
|
T | TTGTGTGT others(11): Show |
1 | a0001c0001t0046g0260 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.196-3370_196-3353d others(20): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181416 | ||||||
| chr5:80181416
|
T | TTGTGTGT others(15): Show |
1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.196-3374_196-3353d others(24): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181416 | ||||||
| chr5:80181416
|
T | TTGTGTGT others(19): Show |
1 | a0001c0001t0013g0140 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.196-3378_196-3353d others(28): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181416 | ||||||
| chr5:80181416
|
TTGTGTGT others(1): Show |
T | 4 | a0001c0001t0001g0133a0001c0001t0007g0249a0001c0002t0003g0096others(1): Show | 4 | HG00140.hp1 HG01261.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-3360_196-3353d others(10): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181416 | ||||||
| chr5:80181450
|
T | A | 101 | a0001c0001t0001g0015a0001c0001t0001g0039a0001c0001t0001g0043others(98): Show | 101 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.196-3386A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181450 | ||||||
| chr5:80181657
|
CT | C | 78 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(75): Show | 78 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.196-3594delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181657 | ||||||
| chr5:80181711
|
G | A | 4 | a0001c0001t0008g0259a0001c0001t0013g0067a0001c0001t0030g0255others(1): Show | 4 | HG03225.hp2 HG03471.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-3647C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80181711 | ||||||
| chr5:80182153
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.196-4089G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182153 | ||||||
| chr5:80182157
|
A | T | 14 | a0001c0001t0001g0103a0001c0001t0001g0177a0001c0001t0002g0104others(11): Show | 14 | HG00609.hp2 HG01496.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.196-4093T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182157 | ||||||
| chr5:80182175
|
G | A | 1 | a0001c0001t0007g0275 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.196-4111C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182175 | ||||||
| chr5:80182254
|
C | T | 2 | a0001c0001t0004g0052a0001c0001t0004g0138 | 2 | HG02145.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.196-4190G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182254 | ||||||
| chr5:80182324
|
G | A | 5 | a0001c0001t0008g0259a0001c0001t0009g0139a0001c0001t0013g0067others(2): Show | 5 | HG02280.hp1 HG03225.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-4260C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182324 | ||||||
| chr5:80182426
|
A | G | 1 | a0001c0001t0043g0234 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.196-4362T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182426 | ||||||
| chr5:80182433
|
A | G | 1 | a0001c0001t0010g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.196-4369T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182433 | ||||||
| chr5:80182541
|
ACCGC | A | 104 | a0001c0001t0001g0015a0001c0001t0001g0039a0001c0001t0001g0043others(101): Show | 104 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.196-4481_196-4478d others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182541 | ||||||
| chr5:80182541
|
ACCGCC | A | 15 | a0001c0001t0009g0126a0001c0001t0010g0235a0001c0001t0013g0140others(12): Show | 15 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.196-4482_196-4478d others(7): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182541 | ||||||
| chr5:80182544
|
G | A | 1 | a0002c0005t0019g0273 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.196-4480C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182544 | ||||||
| chr5:80182544
|
G | C | 4 | a0001c0001t0009g0139a0001c0001t0041g0279a0001c0001t0075g0284others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-4480C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182544 | ||||||
| chr5:80182544
|
G | GC | 49 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0107others(46): Show | 49 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.196-4481dupG | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182544 | ||||||
| chr5:80182544
|
G | GCC | 18 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0153others(15): Show | 18 | HG01978.hp1 HG02145.hp2 HG02273.hp1 others(15): Show |
intron_variant | MODIFIER | c.196-4482_196-4481d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182544 | ||||||
| chr5:80182546
|
C | A | 4 | a0001c0001t0009g0139a0001c0001t0041g0279a0001c0001t0075g0284others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-4482G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182546 | ||||||
| chr5:80182547
|
C | G | 1 | a0001c0001t0002g0237 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.196-4483G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182547 | ||||||
| chr5:80182550
|
C | A | 1 | a0001c0001t0008g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196-4486G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182550 | ||||||
| chr5:80182550
|
C | T | 1 | a0001c0001t0059g0059 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.196-4486G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182550 | ||||||
| chr5:80182551
|
C | A | 12 | a0001c0001t0009g0126a0001c0001t0010g0235a0001c0001t0013g0140others(9): Show | 12 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.196-4487G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182551 | ||||||
| chr5:80182551
|
C | T | 100 | a0001c0001t0001g0015a0001c0001t0001g0039a0001c0001t0001g0043others(97): Show | 100 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.196-4487G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182551 | ||||||
| chr5:80182552
|
C | A | 1 | a0001c0001t0006g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.196-4488G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182552 | ||||||
| chr5:80182553
|
C | A | 1 | a0001c0001t0043g0234 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.196-4489G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182553 | ||||||
| chr5:80182554
|
C | A | 2 | a0001c0001t0043g0234a0001c0002t0031g0001 | 2 | HG02258.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.196-4490G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182554 | ||||||
| chr5:80182555
|
CT | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0187others(4): Show | 7 | HG02135.hp2 NA18955.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.196-4492delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182555 | ||||||
| chr5:80182556
|
T | C | 194 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0028others(191): Show | 194 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.196-4492A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182556 | ||||||
| chr5:80182605
|
G | A | 170 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(167): Show | 170 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.196-4541C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182605 | ||||||
| chr5:80182788
|
C | T | 6 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0150others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-4724G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182788 | ||||||
| chr5:80182789
|
G | A | 1 | a0002c0005t0019g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.196-4725C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182789 | ||||||
| chr5:80182851
|
G | A | 1 | a0001c0001t0011g0245 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.196-4787C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182851 | ||||||
| chr5:80182854
|
C | G | 9 | a0001c0001t0007g0158a0001c0001t0009g0139a0001c0001t0010g0062others(6): Show | 9 | HG02280.hp1 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.196-4790G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182854 | ||||||
| chr5:80182914
|
A | G | 1 | a0001c0001t0002g0215 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.196-4850T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80182914 | ||||||
| chr5:80183107
|
G | A | 2 | a0001c0001t0006g0175a0001c0001t0006g0179 | 2 | HG00733.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.196-5043C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183107 | ||||||
| chr5:80183135
|
G | T | 10 | a0001c0001t0008g0259a0001c0001t0009g0126a0001c0001t0010g0235others(7): Show | 10 | HG01884.hp1 HG02486.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-5071C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183135 | ||||||
| chr5:80183136
|
G | GCTTC | 10 | a0001c0001t0008g0259a0001c0001t0009g0126a0001c0001t0010g0235others(7): Show | 10 | HG01884.hp1 HG02486.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-5073_196-5072i others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183136 | ||||||
| chr5:80183139
|
C | CTTGAAGC others(9): Show |
10 | a0001c0001t0008g0259a0001c0001t0009g0126a0001c0001t0010g0235others(7): Show | 10 | HG01884.hp1 HG02486.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-5076_196-5075i others(18): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183139 | ||||||
| chr5:80183198
|
T | C | 105 | a0001c0001t0001g0015a0001c0001t0001g0039a0001c0001t0001g0043others(102): Show | 105 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.196-5134A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183198 | ||||||
| chr5:80183204
|
G | A | 2 | a0002c0005t0019g0042a0002c0005t0019g0273 | 2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.196-5140C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183204 | ||||||
| chr5:80183242
|
A | G | 2 | a0001c0001t0004g0282a0001c0001t0062g0283 | 2 | HG01943.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.196-5178T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183242 | ||||||
| chr5:80183243
|
C | T | 19 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0150others(16): Show | 19 | HG01243.hp2 HG02055.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.196-5179G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183243 | ||||||
| chr5:80183280
|
C | T | 4 | a0001c0001t0007g0158a0001c0001t0036g0254a0001c0001t0075g0284others(1): Show | 4 | HG02922.hp1 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-5216G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183280 | ||||||
| chr5:80183281
|
C | T | 10 | a0001c0001t0008g0259a0001c0001t0009g0126a0001c0001t0010g0235others(7): Show | 10 | HG01884.hp1 HG02486.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-5217G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183281 | ||||||
| chr5:80183431
|
G | C | 1 | a0002c0005t0019g0273 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.196-5367C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183431 | ||||||
| chr5:80183437
|
G | C | 1 | a0001c0001t0001g0200 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.196-5373C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183437 | ||||||
| chr5:80183444
|
G | C | 1 | a0001c0002t0031g0001 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.196-5380C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183444 | ||||||
| chr5:80183465
|
T | C | 37 | a0001c0001t0002g0277a0001c0001t0002g0278a0001c0001t0006g0064others(34): Show | 37 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.196-5401A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183465 | ||||||
| chr5:80183518
|
C | T | 10 | a0001c0001t0008g0259a0001c0001t0009g0126a0001c0001t0010g0235others(7): Show | 10 | HG01884.hp1 HG02486.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-5454G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183518 | ||||||
| chr5:80183545
|
C | G | 4 | a0001c0001t0007g0158a0001c0001t0036g0254a0001c0001t0075g0284others(1): Show | 4 | HG02922.hp1 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-5481G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183545 | ||||||
| chr5:80183701
|
C | T | 1 | a0002c0004t0005g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.196-5637G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183701 | ||||||
| chr5:80183705
|
C | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0271a0001c0002t0073g0204 | 3 | HG01070.hp1 HG01074.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.196-5641G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183705 | ||||||
| chr5:80183820
|
C | T | 5 | a0001c0001t0009g0139a0001c0001t0010g0062a0001c0001t0041g0279others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-5756G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183820 | ||||||
| chr5:80183894
|
G | GC | 13 | a0001c0001t0002g0278a0001c0001t0007g0142a0001c0001t0008g0129others(10): Show | 13 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.196-5831dupG | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183894 | ||||||
| chr5:80183984
|
A | G | 2 | a0002c0005t0019g0042a0002c0005t0019g0273 | 2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.196-5920T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80183984 | ||||||
| chr5:80184020
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0225 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.196-5956C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80184020 | ||||||
| chr5:80184097
|
G | A | 10 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0150others(7): Show | 10 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-6033C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80184097 | ||||||
| chr5:80184139
|
T | TA | 8 | a0001c0001t0002g0278a0001c0001t0007g0142a0001c0001t0008g0129others(5): Show | 8 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-6076dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80184139 | ||||||
| chr5:80184297
|
A | G | 3 | a0001c0001t0013g0140a0001c0001t0046g0260a0001c0001t0047g0261 | 3 | HG01167.hp2 HG03486.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.196-6233T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80184297 | ||||||
| chr5:80184363
|
G | A | 14 | a0001c0001t0002g0278a0001c0001t0007g0142a0001c0001t0008g0129others(11): Show | 14 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.196-6299C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80184363 | ||||||
| chr5:80184428
|
G | A | 2 | a0001c0001t0004g0020a0001c0001t0004g0021 | 2 | HG00639.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.196-6364C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80184428 | ||||||
| chr5:80184547
|
A | C | 1 | a0001c0001t0007g0249 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.196-6483T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80184547 | ||||||
| chr5:80184549
|
A | G | 1 | a0001c0001t0007g0249 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.196-6485T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80184549 | ||||||
| chr5:80184638
|
A | G | 14 | a0001c0001t0002g0278a0001c0001t0007g0142a0001c0001t0008g0129others(11): Show | 14 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.196-6574T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80184638 | ||||||
| chr5:80184768
|
T | C | 6 | a0001c0001t0009g0139a0001c0001t0010g0062a0001c0001t0041g0279others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-6704A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80184768 | ||||||
| chr5:80184798
|
T | C | 197 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.196-6734A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80184798 | ||||||
| chr5:80184841
|
C | T | 8 | a0001c0001t0002g0278a0001c0001t0007g0142a0001c0001t0008g0129others(5): Show | 8 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-6777G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80184841 | ||||||
| chr5:80185043
|
A | C | 15 | a0001c0001t0002g0278a0001c0001t0007g0142a0001c0001t0008g0129others(12): Show | 15 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.196-6979T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80185043 | ||||||
| chr5:80185100
|
C | G | 12 | a0001c0001t0001g0015a0001c0001t0001g0133a0001c0001t0002g0115others(9): Show | 12 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.196-7036G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80185100 | ||||||
| chr5:80185170
|
C | T | 6 | a0001c0001t0009g0139a0001c0001t0010g0062a0001c0001t0041g0279others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-7106G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80185170 | ||||||
| chr5:80185291
|
T | A | 6 | a0001c0001t0009g0139a0001c0001t0010g0062a0001c0001t0041g0279others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-7227A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80185291 | ||||||
| chr5:80185357
|
C | T | 1 | a0001c0001t0043g0234 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.196-7293G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80185357 | ||||||
| chr5:80185439
|
C | T | 1 | a0001c0001t0060g0017 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.196-7375G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80185439 | ||||||
| chr5:80185540
|
C | CT | 285 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.196-7477dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80185540 | ||||||
| chr5:80185679
|
C | T | 10 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0150others(7): Show | 10 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-7615G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80185679 | ||||||
| chr5:80185689
|
T | C | 6 | a0001c0001t0009g0139a0001c0001t0010g0062a0001c0001t0041g0279others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-7625A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80185689 | ||||||
| chr5:80185825
|
G | A | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.196-7761C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80185825 | ||||||
| chr5:80185902
|
C | T | 1 | a0001c0001t0038g0111 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.196-7838G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80185902 | ||||||
| chr5:80186091
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0225 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.196-8027G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80186091 | ||||||
| chr5:80186126
|
G | GA | 15 | a0001c0001t0001g0151a0001c0001t0001g0162a0001c0001t0002g0094others(12): Show | 15 | HG01109.hp2 HG01891.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.196-8063dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80186126 | ||||||
| chr5:80186126
|
GA | G | 29 | a0001c0001t0001g0045a0001c0001t0001g0213a0001c0001t0002g0134others(26): Show | 29 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.196-8063delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80186126 | ||||||
| chr5:80186126
|
GAA | G | 26 | a0001c0001t0001g0015a0001c0001t0001g0133a0001c0001t0002g0056others(23): Show | 26 | HG00140.hp1 HG00741.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.196-8064_196-8063d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80186126 | ||||||
| chr5:80186126
|
GAAA | G | 65 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0089others(62): Show | 65 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.196-8065_196-8063d others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80186126 | ||||||
| chr5:80186126
|
GAAAA | G | 71 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(68): Show | 71 | HG00408.hp1 HG00642.hp1 HG01167.hp1 others(68): Show |
intron_variant | MODIFIER | c.196-8066_196-8063d others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80186126 | ||||||
| chr5:80186126
|
GAAAAA | G | 10 | a0001c0001t0001g0269a0001c0001t0002g0277a0001c0001t0006g0064others(7): Show | 10 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-8067_196-8063d others(7): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80186126 | ||||||
| chr5:80186126
|
GAAAAAAA others(3): Show |
G | 2 | a0001c0001t0001g0216a0001c0002t0031g0001 | 2 | NA19009.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.196-8072_196-8063d others(12): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80186126 | ||||||
| chr5:80186126
|
GAAAAAAA others(4): Show |
G | 3 | a0001c0001t0013g0140a0001c0001t0046g0260a0001c0001t0047g0261 | 3 | HG01167.hp2 HG03486.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.196-8073_196-8063d others(13): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80186126 | ||||||
| chr5:80186126
|
GAAAAAAA others(6): Show |
G | 3 | a0001c0001t0007g0069a0001c0001t0007g0275a0001c0001t0008g0182 | 3 | HG02145.hp2 HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.196-8075_196-8063d others(15): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80186126 | ||||||
| chr5:80186126
|
GAAAAAAA others(7): Show |
G | 10 | a0001c0001t0002g0044a0001c0001t0006g0023a0001c0001t0008g0129others(7): Show | 10 | HG00099.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-8076_196-8063d others(16): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80186126 | ||||||
| chr5:80186258
|
T | C | 2 | a0002c0005t0019g0042a0002c0005t0019g0273 | 2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.196-8194A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80186258 | ||||||
| chr5:80186378
|
T | C | 6 | a0001c0001t0009g0139a0001c0001t0010g0062a0001c0001t0041g0279others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-8314A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80186378 | ||||||
| chr5:80186401
|
G | A | 6 | a0001c0001t0009g0139a0001c0001t0010g0062a0001c0001t0041g0279others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-8337C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80186401 | ||||||
| chr5:80186564
|
A | T | 172 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(169): Show | 172 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.196-8500T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80186564 | ||||||
| chr5:80186651
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.196-8587C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80186651 | ||||||
| chr5:80186981
|
C | T | 93 | a0001c0001t0001g0015a0001c0001t0001g0039a0001c0001t0001g0043others(90): Show | 93 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.196-8917G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80186981 | ||||||
| chr5:80187040
|
T | G | 1 | a0001c0001t0008g0259 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.196-8976A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80187040 | ||||||
| chr5:80187059
|
A | G | 6 | a0001c0001t0009g0139a0001c0001t0010g0062a0001c0001t0041g0279others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-8995T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80187059 | ||||||
| chr5:80187143
|
G | T | 32 | a0001c0001t0001g0089a0001c0001t0002g0056a0001c0001t0002g0101others(29): Show | 32 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.196-9079C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80187143 | ||||||
| chr5:80187165
|
C | T | 1 | a0001c0001t0008g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.196-9101G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80187165 | ||||||
| chr5:80187248
|
A | C | 1 | a0001c0001t0002g0197 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.196-9184T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80187248 | ||||||
| chr5:80187378
|
T | C | 210 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(207): Show | 210 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.196-9314A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80187378 | ||||||
| chr5:80187481
|
G | A | 8 | a0001c0001t0002g0278a0001c0001t0007g0142a0001c0001t0008g0129others(5): Show | 8 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-9417C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80187481 | ||||||
| chr5:80187619
|
A | G | 1 | a0001c0001t0038g0111 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.196-9555T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80187619 | ||||||
| chr5:80187881
|
G | A | 2 | a0001c0001t0009g0226a0001c0001t0066g0172 | 2 | HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.196-9817C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80187881 | ||||||
| chr5:80187941
|
C | T | 6 | a0001c0001t0009g0139a0001c0001t0010g0062a0001c0001t0041g0279others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-9877G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80187941 | ||||||
| chr5:80188004
|
G | T | 2 | a0001c0001t0004g0282a0001c0001t0062g0283 | 2 | HG01943.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.196-9940C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188004 | ||||||
| chr5:80188083
|
G | C | 4 | a0001c0001t0009g0139a0001c0001t0041g0279a0001c0006t0020g0127others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-10019C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188083 | ||||||
| chr5:80188152
|
G | A | 6 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0150others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-10088C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188152 | ||||||
| chr5:80188201
|
T | C | 1 | a0001c0001t0076g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.196-10137A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188201 | ||||||
| chr5:80188208
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0025g0050a0001c0001t0025g0051 | 3 | HG03195.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.196-10144C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188208 | ||||||
| chr5:80188282
|
C | CA | 12 | a0001c0001t0001g0121a0001c0001t0001g0216a0001c0001t0002g0044others(9): Show | 12 | HG00639.hp1 HG02622.hp1 HG03688.hp1 others(9): Show |
intron_variant | MODIFIER | c.196-10219dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188282 | ||||||
| chr5:80188282
|
CA | C | 163 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0014others(160): Show | 163 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.196-10219delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188282 | ||||||
| chr5:80188282
|
CAA | C | 17 | a0001c0001t0002g0115a0001c0001t0006g0064a0001c0001t0007g0150others(14): Show | 17 | HG01070.hp2 HG02055.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.196-10220_196-1021 others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188282 | ||||||
| chr5:80188282
|
CAAA | C | 9 | a0001c0001t0002g0278a0001c0001t0007g0142a0001c0001t0008g0129others(6): Show | 9 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-10221_196-1021 others(7): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188282 | ||||||
| chr5:80188326
|
C | T | 5 | a0001c0001t0009g0139a0001c0001t0010g0062a0001c0001t0041g0279others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-10262G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188326 | ||||||
| chr5:80188360
|
TTA | T | 5 | a0001c0001t0009g0139a0001c0001t0010g0062a0001c0001t0041g0279others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-10298_196-1029 others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188360 | ||||||
| chr5:80188437
|
A | G | 5 | a0001c0001t0009g0139a0001c0001t0010g0062a0001c0001t0041g0279others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-10373T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188437 | ||||||
| chr5:80188450
|
T | C | 3 | a0001c0001t0013g0068a0001c0001t0044g0149a0001c0001t0050g0265 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.196-10386A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188450 | ||||||
| chr5:80188720
|
T | G | 1 | a0001c0001t0001g0029 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.196-10656A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188720 | ||||||
| chr5:80188754
|
G | A | 72 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(69): Show | 72 | HG00408.hp1 HG00438.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.196-10690C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188754 | ||||||
| chr5:80188883
|
G | A | 4 | a0001c0001t0021g0053a0001c0001t0021g0141a0002c0005t0019g0042others(1): Show | 4 | HG02965.hp1 HG03139.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-10819C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188883 | ||||||
| chr5:80188935
|
T | C | 2 | a0001c0001t0021g0053a0001c0001t0021g0141 | 2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.196-10871A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188935 | ||||||
| chr5:80188996
|
T | C | 3 | a0001c0002t0003g0222a0001c0002t0072g0210a0001c0002t0077g0285 | 3 | HG03239.hp1 HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.196-10932A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80188996 | ||||||
| chr5:80189092
|
G | C | 2 | a0001c0002t0003g0040a0001c0002t0016g0033 | 2 | NA18942.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.196-11028C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80189092 | ||||||
| chr5:80189126
|
T | C | 6 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0150others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-11062A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80189126 | ||||||
| chr5:80189137
|
A | G | 93 | a0001c0001t0001g0015a0001c0001t0001g0039a0001c0001t0001g0043others(90): Show | 93 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.196-11073T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80189137 | ||||||
| chr5:80189184
|
A | G | 2 | a0001c0001t0021g0053a0001c0001t0021g0141 | 2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.196-11120T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80189184 | ||||||
| chr5:80189355
|
G | C | 2 | a0001c0002t0068g0188a0001c0002t0070g0189 | 2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.196-11291C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80189355 | ||||||
| chr5:80189494
|
C | T | 3 | a0001c0001t0020g0057a0001c0001t0059g0059a0001c0002t0005g0058 | 3 | HG01243.hp1 HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.196-11430G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80189494 | ||||||
| chr5:80189669
|
T | C | 1 | a0001c0001t0008g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196-11605A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80189669 | ||||||
| chr5:80189809
|
G | T | 156 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(153): Show | 156 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.196-11745C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80189809 | ||||||
| chr5:80190010
|
C | A | 1 | a0001c0001t0001g0170 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.196-11946G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80190010 | ||||||
| chr5:80190042
|
G | T | 10 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0150others(7): Show | 10 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-11978C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80190042 | ||||||
| chr5:80190106
|
C | CT | 20 | a0001c0001t0001g0022a0001c0001t0001g0216a0001c0001t0002g0024others(17): Show | 20 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.196-12043dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80190106 | ||||||
| chr5:80190106
|
C | CTT | 18 | a0001c0001t0002g0278a0001c0001t0006g0114a0001c0001t0006g0135others(15): Show | 18 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.196-12044_196-1204 others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80190106 | ||||||
| chr5:80190106
|
CT | C | 39 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0002g0163others(36): Show | 39 | HG00639.hp2 HG01071.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.196-12043delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80190106 | ||||||
| chr5:80190106
|
CTT | C | 154 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(151): Show | 154 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.196-12044_196-1204 others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80190106 | ||||||
| chr5:80190256
|
G | C | 1 | a0001c0001t0066g0172 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.196-12192C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80190256 | ||||||
| chr5:80190309
|
C | T | 2 | a0001c0001t0021g0053a0001c0001t0021g0141 | 2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.196-12245G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80190309 | ||||||
| chr5:80190310
|
G | A | 1 | a0001c0001t0043g0234 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.196-12246C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80190310 | ||||||
| chr5:80190382
|
G | C | 1 | a0001c0001t0010g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.196-12318C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80190382 | ||||||
| chr5:80190501
|
G | T | 154 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(151): Show | 154 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.195+12385C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80190501 | ||||||
| chr5:80190508
|
C | T | 5 | a0001c0001t0009g0139a0001c0001t0010g0062a0001c0001t0041g0279others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+12378G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80190508 | ||||||
| chr5:80190575
|
A | T | 1 | a0001c0002t0003g0193 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.195+12311T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80190575 | ||||||
| chr5:80190584
|
A | T | 27 | a0001c0001t0001g0216a0001c0001t0002g0094a0001c0001t0006g0114others(24): Show | 27 | HG00323.hp2 HG00733.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.195+12302T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80190584 | ||||||
| chr5:80190827
|
G | T | 3 | a0001c0001t0013g0140a0001c0001t0046g0260a0001c0001t0047g0261 | 3 | HG01167.hp2 HG03486.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.195+12059C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80190827 | ||||||
| chr5:80190946
|
C | T | 2 | a0001c0001t0018g0002a0001c0001t0018g0003 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.195+11940G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80190946 | ||||||
| chr5:80190959
|
C | CA | 285 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.195+11926dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80190959 | ||||||
| chr5:80191038
|
C | T | 4 | a0001c0001t0009g0139a0001c0001t0010g0062a0001c0001t0041g0279others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+11848G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191038 | ||||||
| chr5:80191166
|
CCT | C | 140 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(137): Show | 140 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.195+11718_195+1171 others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191166 | ||||||
| chr5:80191175
|
T | C | 1 | a0001c0001t0002g0248 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.195+11711A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191175 | ||||||
| chr5:80191275
|
T | C | 2 | a0001c0001t0004g0171a0001c0001t0004g0199 | 2 | HG01361.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.195+11611A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191275 | ||||||
| chr5:80191326
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.195+11560C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191326 | ||||||
| chr5:80191353
|
G | A | 151 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(148): Show | 151 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.195+11533C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191353 | ||||||
| chr5:80191428
|
A | G | 5 | a0001c0001t0009g0139a0001c0001t0010g0062a0001c0001t0041g0279others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+11458T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191428 | ||||||
| chr5:80191476
|
C | G | 2 | a0001c0006t0020g0127a0001c0006t0045g0128 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.195+11410G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191476 | ||||||
| chr5:80191493
|
A | G | 2 | a0001c0001t0009g0139a0001c0001t0041g0279 | 2 | HG02280.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.195+11393T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191493 | ||||||
| chr5:80191496
|
G | A | 15 | a0001c0001t0001g0089a0001c0001t0001g0200a0001c0001t0002g0027others(12): Show | 15 | HG01261.hp1 HG02015.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.195+11390C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191496 | ||||||
| chr5:80191496
|
GA | G | 165 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(162): Show | 165 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.195+11389delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191496 | ||||||
| chr5:80191497
|
A | G | 13 | a0001c0001t0001g0089a0001c0001t0001g0200a0001c0001t0002g0027others(10): Show | 13 | HG01261.hp1 HG02015.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.195+11389T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191497 | ||||||
| chr5:80191548
|
C | T | 1 | a0001c0002t0003g0108 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.195+11338G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191548 | ||||||
| chr5:80191599
|
C | T | 1 | a0001c0002t0003g0193 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.195+11287G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191599 | ||||||
| chr5:80191663
|
TA | T | 61 | a0001c0001t0001g0043a0001c0001t0001g0194a0001c0001t0001g0271others(58): Show | 61 | HG00735.hp2 HG01069.hp1 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.195+11222delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191663 | ||||||
| chr5:80191663
|
TAA | T | 8 | a0001c0001t0002g0278a0001c0001t0007g0142a0001c0001t0008g0129others(5): Show | 8 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.195+11221_195+1122 others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191663 | ||||||
| chr5:80191681
|
G | GA | 13 | a0001c0001t0002g0278a0001c0001t0007g0142a0001c0001t0008g0129others(10): Show | 13 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.195+11204dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191681 | ||||||
| chr5:80191695
|
C | CT | 6 | a0001c0001t0001g0177a0001c0002t0003g0168a0001c0002t0003g0186others(3): Show | 6 | HG01496.hp2 HG01975.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+11190dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191695 | ||||||
| chr5:80191695
|
CT | C | 17 | a0001c0001t0002g0109a0001c0001t0002g0278a0001c0001t0002g0280others(14): Show | 17 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.195+11190delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191695 | ||||||
| chr5:80191817
|
T | C | 3 | a0001c0001t0002g0219a0001c0001t0004g0073a0001c0001t0004g0221 | 3 | HG02071.hp1 NA19074.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.195+11069A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191817 | ||||||
| chr5:80191890
|
T | C | 163 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.195+10996A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80191890 | ||||||
| chr5:80192014
|
A | G | 8 | a0001c0001t0007g0069a0001c0001t0007g0275a0001c0001t0008g0182others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+10872T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80192014 | ||||||
| chr5:80192079
|
T | A | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.195+10807A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80192079 | ||||||
| chr5:80192099
|
G | A | 8 | a0001c0001t0007g0069a0001c0001t0007g0275a0001c0001t0008g0182others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+10787C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80192099 | ||||||
| chr5:80192154
|
A | G | 8 | a0001c0001t0007g0069a0001c0001t0007g0275a0001c0001t0008g0182others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+10732T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80192154 | ||||||
| chr5:80192203
|
T | C | 1 | a0001c0001t0041g0279 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.195+10683A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80192203 | ||||||
| chr5:80192345
|
C | T | 1 | a0001c0001t0065g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.195+10541G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80192345 | ||||||
| chr5:80192370
|
C | T | 159 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(156): Show | 159 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.195+10516G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80192370 | ||||||
| chr5:80192435
|
A | AT | 26 | a0001c0001t0001g0043a0001c0001t0001g0194a0001c0001t0001g0271others(23): Show | 26 | HG00735.hp2 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.195+10450dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80192435 | ||||||
| chr5:80192435
|
AT | A | 68 | a0001c0001t0001g0015a0001c0001t0001g0089a0001c0001t0001g0133others(65): Show | 68 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.195+10450delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80192435 | ||||||
| chr5:80192499
|
T | C | 2 | a0001c0001t0018g0002a0001c0001t0018g0003 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.195+10387A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80192499 | ||||||
| chr5:80192591
|
G | A | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.195+10295C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80192591 | ||||||
| chr5:80192645
|
C | A | 1 | a0001c0001t0012g0131 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.195+10241G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80192645 | ||||||
| chr5:80192654
|
G | A | 3 | a0001c0001t0013g0068a0001c0001t0044g0149a0001c0001t0050g0265 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.195+10232C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80192654 | ||||||
| chr5:80192752
|
T | C | 152 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(149): Show | 152 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.195+10134A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80192752 | ||||||
| chr5:80192790
|
C | G | 1 | a0001c0001t0010g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.195+10096G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80192790 | ||||||
| chr5:80192864
|
C | A | 16 | a0001c0001t0002g0278a0001c0001t0007g0069a0001c0001t0007g0142others(13): Show | 16 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.195+10022G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80192864 | ||||||
| chr5:80192886
|
G | C | 1 | a0001c0001t0009g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.195+10000C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80192886 | ||||||
| chr5:80193028
|
A | C | 1 | a0001c0001t0021g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.195+9858T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80193028 | ||||||
| chr5:80193319
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.195+9567G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80193319 | ||||||
| chr5:80193349
|
C | T | 4 | a0001c0001t0002g0109a0001c0001t0002g0280a0001c0001t0007g0281others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+9537G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80193349 | ||||||
| chr5:80193537
|
C | A | 1 | a0001c0002t0017g0075 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.195+9349G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80193537 | ||||||
| chr5:80193657
|
G | T | 15 | a0001c0001t0002g0278a0001c0001t0007g0069a0001c0001t0007g0142others(12): Show | 15 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.195+9229C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80193657 | ||||||
| chr5:80193693
|
A | G | 220 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(217): Show | 220 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.195+9193T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80193693 | ||||||
| chr5:80193774
|
G | T | 1 | a0001c0001t0009g0226 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.195+9112C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80193774 | ||||||
| chr5:80193863
|
C | T | 3 | a0001c0001t0013g0140a0001c0001t0046g0260a0001c0001t0047g0261 | 3 | HG01167.hp2 HG03486.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.195+9023G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80193863 | ||||||
| chr5:80194032
|
G | A | 16 | a0001c0001t0002g0278a0001c0001t0007g0069a0001c0001t0007g0142others(13): Show | 16 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.195+8854C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80194032 | ||||||
| chr5:80194091
|
G | C | 16 | a0001c0001t0002g0278a0001c0001t0007g0069a0001c0001t0007g0142others(13): Show | 16 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.195+8795C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80194091 | ||||||
| chr5:80194146
|
C | A | 1 | a0001c0001t0032g0004 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.195+8740G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80194146 | ||||||
| chr5:80194264
|
GGA | G | 16 | a0001c0001t0002g0278a0001c0001t0007g0069a0001c0001t0007g0142others(13): Show | 16 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.195+8620_195+8621d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80194264 | ||||||
| chr5:80194266
|
A | G | 1 | a0001c0001t0021g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.195+8620T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80194266 | ||||||
| chr5:80194278
|
T | C | 3 | a0001c0001t0001g0045a0001c0001t0025g0050a0001c0001t0025g0051 | 3 | HG03195.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.195+8608A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80194278 | ||||||
| chr5:80194303
|
G | A | 1 | a0001c0002t0003g0031 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.195+8583C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80194303 | ||||||
| chr5:80194306
|
CCT | C | 16 | a0001c0001t0002g0278a0001c0001t0007g0069a0001c0001t0007g0142others(13): Show | 16 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.195+8578_195+8579d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80194306 | ||||||
| chr5:80194323
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0216others(2): Show | 5 | NA18952.hp1 NA19003.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+8563C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80194323 | ||||||
| chr5:80194404
|
T | C | 1 | a0001c0002t0003g0186 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.195+8482A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80194404 | ||||||
| chr5:80194467
|
T | C | 4 | a0001c0001t0008g0259a0001c0001t0013g0067a0001c0001t0030g0255others(1): Show | 4 | HG03225.hp2 HG03471.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+8419A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80194467 | ||||||
| chr5:80194687
|
C | T | 11 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(8): Show | 11 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+8199G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80194687 | ||||||
| chr5:80194718
|
C | A | 9 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0150others(6): Show | 9 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.195+8168G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80194718 | ||||||
| chr5:80194718
|
C | T | 1 | a0001c0001t0012g0131 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.195+8168G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80194718 | ||||||
| chr5:80194799
|
C | G | 39 | a0001c0001t0001g0043a0001c0001t0001g0194a0001c0001t0001g0271others(36): Show | 39 | HG00735.hp2 HG01069.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.195+8087G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80194799 | ||||||
| chr5:80194868
|
C | T | 2 | a0001c0001t0009g0208a0001c0001t0048g0143 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.195+8018G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80194868 | ||||||
| chr5:80195143
|
G | C | 5 | a0001c0001t0013g0068a0001c0001t0044g0149a0001c0001t0050g0265others(2): Show | 5 | HG02257.hp1 HG02895.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+7743C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80195143 | ||||||
| chr5:80195285
|
G | A | 1 | a0001c0001t0001g0007 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.195+7601C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80195285 | ||||||
| chr5:80195285
|
G | T | 16 | a0001c0001t0002g0278a0001c0001t0007g0069a0001c0001t0007g0142others(13): Show | 16 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.195+7601C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80195285 | ||||||
| chr5:80195286
|
C | CA | 23 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0045others(20): Show | 23 | HG00099.hp2 HG00639.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.195+7599dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80195286 | ||||||
| chr5:80195286
|
C | CAA | 17 | a0001c0001t0002g0278a0001c0001t0007g0069a0001c0001t0007g0142others(14): Show | 17 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.195+7598_195+7599d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80195286 | ||||||
| chr5:80195383
|
A | T | 16 | a0001c0001t0002g0278a0001c0001t0007g0069a0001c0001t0007g0142others(13): Show | 16 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.195+7503T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80195383 | ||||||
| chr5:80195442
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.195+7444G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80195442 | ||||||
| chr5:80195530
|
C | T | 1 | a0001c0001t0015g0256 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.195+7356G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80195530 | ||||||
| chr5:80195643
|
T | G | 17 | a0001c0001t0002g0278a0001c0001t0007g0069a0001c0001t0007g0142others(14): Show | 17 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.195+7243A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80195643 | ||||||
| chr5:80195672
|
T | C | 2 | a0001c0001t0051g0236a0001c0001t0052g0055 | 2 | HG02257.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.195+7214A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80195672 | ||||||
| chr5:80195814
|
T | G | 17 | a0001c0001t0002g0278a0001c0001t0007g0069a0001c0001t0007g0142others(14): Show | 17 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.195+7072A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80195814 | ||||||
| chr5:80195830
|
T | C | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.195+7056A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80195830 | ||||||
| chr5:80195893
|
A | T | 9 | a0001c0001t0007g0158a0001c0001t0009g0126a0001c0001t0010g0235others(6): Show | 9 | HG01884.hp1 HG02486.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.195+6993T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80195893 | ||||||
| chr5:80195972
|
A | G | 17 | a0001c0001t0002g0278a0001c0001t0007g0069a0001c0001t0007g0142others(14): Show | 17 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.195+6914T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80195972 | ||||||
| chr5:80196010
|
T | G | 164 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.195+6876A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196010 | ||||||
| chr5:80196042
|
A | G | 162 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.195+6844T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196042 | ||||||
| chr5:80196059
|
T | C | 1 | a0001c0002t0003g0026 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.195+6827A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196059 | ||||||
| chr5:80196130
|
C | T | 1 | a0001c0001t0006g0114 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.195+6756G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196130 | ||||||
| chr5:80196218
|
GA | G | 6 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0150others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+6667delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196218 | ||||||
| chr5:80196224
|
A | T | 149 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(146): Show | 149 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.195+6662T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196224 | ||||||
| chr5:80196319
|
C | G | 11 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(8): Show | 11 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+6567G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196319 | ||||||
| chr5:80196378
|
G | A | 2 | a0002c0005t0019g0042a0002c0005t0019g0273 | 2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.195+6508C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196378 | ||||||
| chr5:80196479
|
T | C | 12 | a0001c0001t0001g0045a0001c0001t0001g0089a0001c0001t0002g0056others(9): Show | 12 | HG00639.hp1 HG01069.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.195+6407A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196479 | ||||||
| chr5:80196496
|
A | G | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.195+6390T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196496 | ||||||
| chr5:80196512
|
G | A | 74 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(71): Show | 74 | HG00408.hp1 HG00438.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.195+6374C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196512 | ||||||
| chr5:80196562
|
T | C | 1 | a0001c0001t0076g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.195+6324A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196562 | ||||||
| chr5:80196638
|
T | G | 6 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0150others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+6248A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196638 | ||||||
| chr5:80196686
|
C | T | 7 | a0001c0001t0009g0126a0001c0001t0010g0235a0001c0001t0037g0262others(4): Show | 7 | HG00741.hp2 HG01884.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+6200G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196686 | ||||||
| chr5:80196710
|
G | A | 1 | a0001c0002t0031g0001 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.195+6176C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196710 | ||||||
| chr5:80196840
|
C | T | 2 | a0002c0005t0019g0042a0002c0005t0019g0273 | 2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.195+6046G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196840 | ||||||
| chr5:80196854
|
C | T | 1 | a0001c0001t0021g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.195+6032G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196854 | ||||||
| chr5:80196917
|
G | C | 2 | a0002c0005t0019g0042a0002c0005t0019g0273 | 2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.195+5969C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196917 | ||||||
| chr5:80196994
|
A | AT | 141 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0015others(138): Show | 141 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.195+5891dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80196994 | ||||||
| chr5:80197124
|
A | G | 125 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0015others(122): Show | 125 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.195+5762T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197124 | ||||||
| chr5:80197282
|
A | G | 199 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0015others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.195+5604T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197282 | ||||||
| chr5:80197308
|
T | TGA | 4 | a0001c0001t0001g0089a0001c0001t0002g0120a0001c0001t0029g0102others(1): Show | 4 | HG00099.hp1 HG02015.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+5576_195+5577d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197308 | ||||||
| chr5:80197308
|
T | TGAGA | 6 | a0001c0001t0002g0056a0001c0001t0008g0125a0001c0001t0021g0053others(3): Show | 6 | HG02071.hp2 HG02622.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+5574_195+5577d others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197308 | ||||||
| chr5:80197308
|
TGA | T | 9 | a0001c0001t0001g0103a0001c0001t0001g0232a0001c0001t0002g0157others(6): Show | 9 | HG00741.hp1 HG01069.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.195+5576_195+5577d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197308 | ||||||
| chr5:80197308
|
TGAGA | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0092a0001c0001t0001g0216others(10): Show | 13 | HG00438.hp1 HG00735.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.195+5574_195+5577d others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197308 | ||||||
| chr5:80197308
|
TGAGAGA | T | 27 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0039others(24): Show | 27 | HG00323.hp1 HG00609.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.195+5572_195+5577d others(8): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197308 | ||||||
| chr5:80197308
|
TGAGAGAG others(1): Show |
T | 6 | a0001c0001t0004g0021a0001c0001t0026g0070a0001c0001t0026g0244others(3): Show | 6 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+5570_195+5577d others(10): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197308 | ||||||
| chr5:80197308
|
TGAGAGAG others(3): Show |
T | 12 | a0001c0001t0004g0171a0001c0001t0004g0199a0001c0001t0006g0178others(9): Show | 12 | HG00323.hp2 HG01175.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.195+5568_195+5577d others(12): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197308 | ||||||
| chr5:80197308
|
TGAGAGAG others(5): Show |
T | 3 | a0001c0001t0010g0062a0002c0005t0019g0042a0002c0005t0019g0273 | 3 | HG03139.hp1 HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.195+5566_195+5577d others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197308 | ||||||
| chr5:80197308
|
TGAGAGAG others(7): Show |
T | 1 | a0001c0001t0008g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.195+5564_195+5577d others(16): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197308 | ||||||
| chr5:80197308
|
TGAGAGAG others(9): Show |
T | 1 | a0001c0001t0008g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.195+5562_195+5577d others(18): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197308 | ||||||
| chr5:80197308
|
TGAGAGAG others(11): Show |
T | 5 | a0001c0001t0009g0139a0001c0001t0033g0060a0001c0002t0022g0272others(2): Show | 5 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+5560_195+5577d others(20): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197308 | ||||||
| chr5:80197308
|
TGAGAGAG others(13): Show |
T | 3 | a0001c0001t0013g0140a0001c0001t0021g0141a0001c0001t0047g0261 | 3 | HG01167.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.195+5558_195+5577d others(22): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197308 | ||||||
| chr5:80197308
|
TGAGAGAG others(15): Show |
T | 8 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0069others(5): Show | 8 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+5556_195+5577d others(24): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197308 | ||||||
| chr5:80197308
|
TGAGAGAG others(29): Show |
T | 1 | a0001c0002t0003g0041 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.195+5542_195+5577d others(38): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197308 | ||||||
| chr5:80197308
|
TGAGAGAG others(31): Show |
T | 180 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0015others(177): Show | 180 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.195+5540_195+5577d others(40): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197308 | ||||||
| chr5:80197310
|
A | T | 1 | a0001c0001t0002g0112 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.195+5576T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197310 | ||||||
| chr5:80197363
|
G | C | 1 | a0001c0001t0013g0140 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.195+5523C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197363 | ||||||
| chr5:80197366
|
C | T | 8 | a0001c0001t0007g0069a0001c0001t0007g0275a0001c0001t0008g0182others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+5520G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197366 | ||||||
| chr5:80197370
|
C | A | 2 | a0001c0001t0037g0262a0001c0001t0046g0260 | 2 | NA20129.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.195+5516G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197370 | ||||||
| chr5:80197407
|
A | T | 28 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0069others(25): Show | 28 | HG00741.hp2 HG01167.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.195+5479T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197407 | ||||||
| chr5:80197410
|
C | T | 1 | a0001c0002t0003g0087 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.195+5476G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197410 | ||||||
| chr5:80197458
|
C | T | 3 | a0001c0001t0013g0068a0001c0001t0044g0149a0001c0001t0050g0265 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.195+5428G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197458 | ||||||
| chr5:80197716
|
T | C | 1 | a0001c0001t0038g0111 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.195+5170A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197716 | ||||||
| chr5:80197781
|
G | A | 9 | a0001c0001t0007g0158a0001c0001t0009g0126a0001c0001t0010g0235others(6): Show | 9 | HG00741.hp2 HG01884.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.195+5105C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197781 | ||||||
| chr5:80197807
|
T | C | 82 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(79): Show | 82 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.195+5079A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197807 | ||||||
| chr5:80197853
|
C | T | 81 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(78): Show | 81 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.195+5033G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197853 | ||||||
| chr5:80197989
|
A | G | 209 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0015others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.195+4897T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80197989 | ||||||
| chr5:80198074
|
G | C | 76 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(73): Show | 76 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.195+4812C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80198074 | ||||||
| chr5:80198178
|
G | A | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.195+4708C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80198178 | ||||||
| chr5:80198200
|
T | C | 82 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(79): Show | 82 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.195+4686A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80198200 | ||||||
| chr5:80198329
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0007g0249 | 2 | HG00140.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.195+4557G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80198329 | ||||||
| chr5:80198367
|
G | A | 1 | a0001c0001t0021g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.195+4519C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80198367 | ||||||
| chr5:80198416
|
A | C | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.195+4470T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80198416 | ||||||
| chr5:80198438
|
C | T | 29 | a0001c0001t0001g0043a0001c0001t0001g0271a0001c0001t0002g0047others(26): Show | 29 | HG01070.hp1 HG01074.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.195+4448G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80198438 | ||||||
| chr5:80198564
|
T | C | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.195+4322A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80198564 | ||||||
| chr5:80198662
|
C | T | 2 | a0001c0001t0004g0020a0001c0001t0004g0021 | 2 | HG00639.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.195+4224G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80198662 | ||||||
| chr5:80198663
|
G | A | 1 | a0001c0001t0008g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.195+4223C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80198663 | ||||||
| chr5:80198738
|
C | T | 2 | a0001c0001t0038g0111a0002c0003t0009g0228 | 2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.195+4148G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80198738 | ||||||
| chr5:80198798
|
A | G | 9 | a0001c0001t0007g0158a0001c0001t0009g0126a0001c0001t0010g0235others(6): Show | 9 | HG00741.hp2 HG01884.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.195+4088T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80198798 | ||||||
| chr5:80198807
|
G | C | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.195+4079C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80198807 | ||||||
| chr5:80198813
|
A | G | 1 | a0001c0001t0041g0279 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.195+4073T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80198813 | ||||||
| chr5:80198976
|
C | A | 82 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(79): Show | 82 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.195+3910G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80198976 | ||||||
| chr5:80199243
|
T | C | 82 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(79): Show | 82 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.195+3643A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80199243 | ||||||
| chr5:80199363
|
C | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0133a0001c0001t0002g0115others(9): Show | 12 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.195+3523G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80199363 | ||||||
| chr5:80199529
|
C | T | 42 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0001g0269others(39): Show | 42 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.195+3357G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80199529 | ||||||
| chr5:80199636
|
C | T | 79 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(76): Show | 79 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.195+3250G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80199636 | ||||||
| chr5:80199774
|
T | C | 3 | a0001c0001t0002g0163a0001c0001t0037g0262a0001c0001t0063g0164 | 3 | HG01109.hp2 HG01515.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.195+3112A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80199774 | ||||||
| chr5:80199794
|
G | A | 1 | a0001c0002t0005g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.195+3092C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80199794 | ||||||
| chr5:80199818
|
G | C | 79 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(76): Show | 79 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.195+3068C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80199818 | ||||||
| chr5:80199863
|
A | C | 1 | a0001c0002t0003g0168 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.195+3023T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80199863 | ||||||
| chr5:80199992
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.195+2894G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80199992 | ||||||
| chr5:80200023
|
T | C | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.195+2863A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200023 | ||||||
| chr5:80200122
|
C | T | 71 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0028others(68): Show | 71 | HG00408.hp1 HG00438.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.195+2764G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200122 | ||||||
| chr5:80200139
|
C | T | 78 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(75): Show | 78 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.195+2747G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200139 | ||||||
| chr5:80200144
|
C | T | 79 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(76): Show | 79 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.195+2742G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200144 | ||||||
| chr5:80200151
|
C | CTTA | 79 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(76): Show | 79 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.195+2734_195+2735i others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200151 | ||||||
| chr5:80200260
|
G | T | 1 | a0001c0001t0002g0134 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.195+2626C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200260 | ||||||
| chr5:80200322
|
C | CA | 7 | a0001c0001t0002g0191a0001c0001t0009g0126a0001c0001t0038g0111others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+2563dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200322 | ||||||
| chr5:80200322
|
C | CAA | 32 | a0001c0001t0001g0043a0001c0001t0001g0271a0001c0001t0002g0047others(29): Show | 32 | HG01070.hp1 HG01074.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.195+2562_195+2563d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200322 | ||||||
| chr5:80200322
|
C | CAAA | 45 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0001g0269others(42): Show | 45 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.195+2561_195+2563d others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200322 | ||||||
| chr5:80200322
|
CA | C | 6 | a0001c0001t0007g0069a0001c0001t0007g0275a0001c0001t0008g0182others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+2563delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200322 | ||||||
| chr5:80200355
|
A | C | 79 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(76): Show | 79 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.195+2531T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200355 | ||||||
| chr5:80200355
|
A | G | 174 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(171): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.195+2531T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200355 | ||||||
| chr5:80200402
|
C | T | 79 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(76): Show | 79 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.195+2484G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200402 | ||||||
| chr5:80200435
|
G | T | 87 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0015others(84): Show | 87 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.195+2451C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200435 | ||||||
| chr5:80200451
|
G | A | 79 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(76): Show | 79 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.195+2435C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200451 | ||||||
| chr5:80200485
|
C | CA | 79 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(76): Show | 79 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.195+2400dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200485 | ||||||
| chr5:80200493
|
C | A | 79 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(76): Show | 79 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.195+2393G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200493 | ||||||
| chr5:80200602
|
A | G | 82 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(79): Show | 82 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.195+2284T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200602 | ||||||
| chr5:80200607
|
G | C | 79 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(76): Show | 79 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.195+2279C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200607 | ||||||
| chr5:80200651
|
T | C | 29 | a0001c0001t0001g0043a0001c0001t0001g0271a0001c0001t0002g0047others(26): Show | 29 | HG01070.hp1 HG01074.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.195+2235A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200651 | ||||||
| chr5:80200688
|
A | C | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.195+2198T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200688 | ||||||
| chr5:80200776
|
A | C | 3 | a0001c0001t0002g0163a0001c0001t0037g0262a0001c0001t0063g0164 | 3 | HG01109.hp2 HG01515.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.195+2110T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200776 | ||||||
| chr5:80200830
|
AC | A | 79 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(76): Show | 79 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.195+2055delG | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200830 | ||||||
| chr5:80200865
|
G | A | 30 | a0001c0001t0001g0043a0001c0001t0001g0271a0001c0001t0002g0047others(27): Show | 30 | HG01070.hp1 HG01074.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.195+2021C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200865 | ||||||
| chr5:80200935
|
G | T | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.195+1951C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200935 | ||||||
| chr5:80200943
|
C | T | 84 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0015others(81): Show | 84 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.195+1943G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200943 | ||||||
| chr5:80200960
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.195+1926T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200960 | ||||||
| chr5:80200970
|
G | A | 73 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0028others(70): Show | 73 | HG00408.hp1 HG00438.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.195+1916C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200970 | ||||||
| chr5:80200987
|
T | C | 78 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0151others(75): Show | 78 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.195+1899A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80200987 | ||||||
| chr5:80201054
|
G | A | 1 | a0001c0001t0021g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.195+1832C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201054 | ||||||
| chr5:80201056
|
G | A | 43 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0001g0269others(40): Show | 43 | HG00408.hp2 HG00621.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.195+1830C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201056 | ||||||
| chr5:80201119
|
C | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0028others(69): Show | 72 | HG00408.hp1 HG00438.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.195+1767G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201119 | ||||||
| chr5:80201195
|
G | A | 1 | a0001c0001t0021g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.195+1691C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201195 | ||||||
| chr5:80201201
|
T | C | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.195+1685A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201201 | ||||||
| chr5:80201241
|
G | A | 75 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0028others(72): Show | 75 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.195+1645C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201241 | ||||||
| chr5:80201337
|
T | C | 50 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0001g0269others(47): Show | 50 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.195+1549A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201337 | ||||||
| chr5:80201426
|
C | T | 3 | a0001c0001t0023g0220a0001c0001t0028g0159a0001c0001t0028g0160 | 3 | HG03490.hp1 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.195+1460G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201426 | ||||||
| chr5:80201443
|
T | C | 50 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0001g0269others(47): Show | 50 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.195+1443A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201443 | ||||||
| chr5:80201511
|
T | C | 53 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0001g0269others(50): Show | 53 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.195+1375A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201511 | ||||||
| chr5:80201514
|
A | G | 197 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0028others(194): Show | 197 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.195+1372T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201514 | ||||||
| chr5:80201596
|
C | T | 197 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0028others(194): Show | 197 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.195+1290G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201596 | ||||||
| chr5:80201635
|
C | G | 2 | a0001c0001t0051g0236a0001c0001t0052g0055 | 2 | HG02257.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.195+1251G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201635 | ||||||
| chr5:80201764
|
G | A | 50 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0001g0269others(47): Show | 50 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.195+1122C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201764 | ||||||
| chr5:80201819
|
C | A | 6 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0150others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+1067G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201819 | ||||||
| chr5:80201877
|
G | T | 50 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0001g0269others(47): Show | 50 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.195+1009C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201877 | ||||||
| chr5:80201882
|
A | G | 2 | a0001c0001t0038g0111a0002c0003t0009g0228 | 2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.195+1004T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201882 | ||||||
| chr5:80201885
|
A | G | 1 | a0001c0001t0002g0252 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.195+1001T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201885 | ||||||
| chr5:80201955
|
G | A | 3 | a0001c0001t0002g0163a0001c0001t0037g0262a0001c0001t0063g0164 | 3 | HG01109.hp2 HG01515.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.195+931C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201955 | ||||||
| chr5:80201975
|
G | A | 50 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0001g0269others(47): Show | 50 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.195+911C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80201975 | ||||||
| chr5:80202067
|
G | T | 3 | a0001c0001t0002g0163a0001c0001t0037g0262a0001c0001t0063g0164 | 3 | HG01109.hp2 HG01515.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.195+819C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80202067 | ||||||
| chr5:80202129
|
T | C | 1 | a0001c0001t0044g0149 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.195+757A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80202129 | ||||||
| chr5:80202217
|
A | G | 50 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0001g0269others(47): Show | 50 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.195+669T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80202217 | ||||||
| chr5:80202238
|
C | T | 1 | a0001c0001t0001g0006 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.195+648G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80202238 | ||||||
| chr5:80202361
|
C | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0028others(69): Show | 72 | HG00408.hp1 HG00438.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.195+525G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80202361 | ||||||
| chr5:80202383
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.195+503C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80202383 | ||||||
| chr5:80202461
|
G | A | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.195+425C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80202461 | ||||||
| chr5:80202579
|
T | C | 50 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0001g0269others(47): Show | 50 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.195+307A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80202579 | ||||||
| chr5:80202784
|
A | G | 2 | a0001c0001t0001g0271a0001c0002t0073g0204 | 2 | HG01070.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.195+102T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80202784 | ||||||
| chr5:80202804
|
A | G | 37 | a0001c0001t0001g0121a0001c0001t0002g0094a0001c0001t0002g0163others(34): Show | 37 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.195+82T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80202804 | ||||||
| chr5:80202863
|
G | A | 1 | a0001c0001t0006g0167 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.195+23C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 2/11 | chr5 | 80202863 | ||||||
| chr5:80203206
|
T | C | 2 | a0001c0002t0003g0146a0001c0002t0003g0147 | 2 | NA18942.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.28-153A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80203206 | ||||||
| chr5:80203257
|
C | CAT | 31 | a0001c0001t0001g0121a0001c0001t0002g0094a0001c0001t0002g0219others(28): Show | 31 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.28-206_28-205dupAT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80203257 | ||||||
| chr5:80203257
|
C | CATAT | 90 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.28-208_28-205dupAT others(2): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80203257 | ||||||
| chr5:80203257
|
C | CATATAT | 6 | a0001c0001t0002g0136a0001c0001t0002g0191a0001c0001t0002g0239others(3): Show | 6 | HG02135.hp2 HG03209.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-210_28-205dupAT others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80203257 | ||||||
| chr5:80203257
|
C | CATATATA others(3): Show |
2 | a0001c0006t0020g0127a0001c0006t0045g0128 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.28-214_28-205dupAT others(8): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80203257 | ||||||
| chr5:80203257
|
CAT | C | 6 | a0001c0001t0001g0216a0001c0001t0002g0278a0001c0001t0006g0178others(3): Show | 6 | HG01175.hp2 HG01243.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-206_28-205delAT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80203257 | ||||||
| chr5:80203259
|
T | C | 3 | a0001c0001t0002g0163a0001c0001t0037g0262a0001c0001t0063g0164 | 3 | HG01109.hp2 HG01515.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.28-206A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80203259 | ||||||
| chr5:80203344
|
C | T | 3 | a0001c0001t0013g0068a0001c0001t0044g0149a0001c0001t0050g0265 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.28-291G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80203344 | ||||||
| chr5:80203348
|
T | C | 200 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.28-295A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80203348 | ||||||
| chr5:80203364
|
C | A | 2 | a0001c0001t0013g0140a0001c0001t0047g0261 | 2 | HG01167.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.28-311G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80203364 | ||||||
| chr5:80203459
|
C | T | 1 | a0001c0001t0057g0196 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.28-406G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80203459 | ||||||
| chr5:80203659
|
C | T | 2 | a0001c0001t0002g0155a0001c0001t0002g0156 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.28-606G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80203659 | ||||||
| chr5:80203676
|
C | T | 37 | a0001c0001t0001g0121a0001c0001t0002g0094a0001c0001t0002g0163others(34): Show | 37 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.28-623G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80203676 | ||||||
| chr5:80203706
|
AAACTTCT others(24): Show |
A | 2 | a0001c0001t0025g0050a0001c0001t0025g0051 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.28-684_28-654delAA others(29): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80203706 | ||||||
| chr5:80203723
|
T | A | 1 | a0001c0001t0002g0027 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.28-670A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80203723 | ||||||
| chr5:80203842
|
G | C | 37 | a0001c0001t0001g0043a0001c0001t0002g0047a0001c0001t0002g0097others(34): Show | 37 | HG00735.hp2 HG00741.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.28-789C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80203842 | ||||||
| chr5:80204078
|
C | T | 2 | a0001c0002t0068g0188a0001c0002t0070g0189 | 2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.28-1025G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80204078 | ||||||
| chr5:80204126
|
G | T | 5 | a0001c0001t0007g0069a0001c0001t0007g0275a0001c0001t0008g0182others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-1073C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80204126 | ||||||
| chr5:80204205
|
T | C | 3 | a0001c0001t0020g0057a0001c0001t0059g0059a0001c0002t0005g0058 | 3 | HG01243.hp1 HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.28-1152A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80204205 | ||||||
| chr5:80204387
|
A | T | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-1334T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80204387 | ||||||
| chr5:80204430
|
C | T | 1 | a0001c0001t0002g0169 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.28-1377G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80204430 | ||||||
| chr5:80204545
|
A | G | 7 | a0001c0001t0007g0069a0001c0001t0007g0275a0001c0001t0008g0182others(4): Show | 7 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-1492T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80204545 | ||||||
| chr5:80204571
|
A | G | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.28-1518T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80204571 | ||||||
| chr5:80204585
|
A | G | 3 | a0001c0001t0002g0163a0001c0001t0037g0262a0001c0001t0063g0164 | 3 | HG01109.hp2 HG01515.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.28-1532T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80204585 | ||||||
| chr5:80204675
|
A | C | 1 | a0001c0002t0003g0168 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.28-1622T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80204675 | ||||||
| chr5:80204685
|
G | C | 4 | a0001c0001t0038g0111a0001c0006t0020g0127a0001c0006t0045g0128others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-1632C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80204685 | ||||||
| chr5:80204745
|
T | G | 6 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0150others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-1692A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80204745 | ||||||
| chr5:80204886
|
C | T | 1 | a0001c0002t0027g0274 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.28-1833G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80204886 | ||||||
| chr5:80204927
|
C | A | 1 | a0001c0001t0002g0134 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.28-1874G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80204927 | ||||||
| chr5:80204986
|
G | A | 20 | a0001c0001t0001g0043a0001c0001t0002g0047a0001c0001t0002g0097others(17): Show | 20 | HG00735.hp2 HG01074.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.28-1933C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80204986 | ||||||
| chr5:80205056
|
A | C | 11 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(8): Show | 11 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-2003T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205056 | ||||||
| chr5:80205099
|
T | C | 16 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(13): Show | 16 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-2046A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205099 | ||||||
| chr5:80205322
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.28-2269G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205322 | ||||||
| chr5:80205331
|
A | T | 16 | a0001c0001t0001g0151a0001c0001t0001g0269a0001c0001t0002g0109others(13): Show | 16 | HG01891.hp2 HG02559.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-2278T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205331 | ||||||
| chr5:80205341
|
G | A | 30 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0002g0094others(27): Show | 30 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.28-2288C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205341 | ||||||
| chr5:80205347
|
C | G | 1 | a0001c0001t0010g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.28-2294G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205347 | ||||||
| chr5:80205737
|
T | C | 5 | a0001c0001t0007g0069a0001c0001t0007g0275a0001c0001t0008g0182others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-2684A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205737 | ||||||
| chr5:80205910
|
A | AAAAAC | 14 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(11): Show | 14 | HG00140.hp1 HG00621.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.28-2858_28-2857ins others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205910 | ||||||
| chr5:80205913
|
T | A | 47 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0133others(44): Show | 47 | HG00140.hp1 HG00408.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.28-2860A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205913 | ||||||
| chr5:80205913
|
TACAAAAC others(3): Show |
T | 5 | a0001c0001t0007g0069a0001c0001t0007g0275a0001c0001t0008g0182others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-2870_28-2861del others(10): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205913 | ||||||
| chr5:80205975
|
C | CA | 16 | a0001c0001t0001g0271a0001c0001t0002g0056a0001c0001t0007g0150others(13): Show | 16 | HG00438.hp1 HG00609.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-2923dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205975 | ||||||
| chr5:80205975
|
C | CAA | 47 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0043others(44): Show | 47 | HG00621.hp2 HG00735.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.28-2924_28-2923dup others(2): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205975 | ||||||
| chr5:80205975
|
C | CAAA | 60 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0029others(57): Show | 60 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.28-2925_28-2923dup others(3): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205975 | ||||||
| chr5:80205975
|
C | CAAAA | 9 | a0001c0001t0001g0162a0001c0001t0001g0190a0001c0001t0001g0213others(6): Show | 9 | HG01975.hp2 HG02129.hp1 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.28-2926_28-2923dup others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205975 | ||||||
| chr5:80205975
|
CA | C | 8 | a0001c0001t0001g0014a0001c0001t0002g0163a0001c0001t0013g0140others(5): Show | 8 | HG01109.hp2 HG01167.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-2923delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205975 | ||||||
| chr5:80205975
|
CAA | C | 14 | a0001c0001t0001g0151a0001c0001t0001g0269a0001c0001t0002g0270others(11): Show | 14 | HG01891.hp2 HG02559.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.28-2924_28-2923del others(2): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205975 | ||||||
| chr5:80205996
|
C | A | 1 | a0001c0001t0010g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.28-2943G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205996 | ||||||
| chr5:80205996
|
C | T | 33 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0002g0094others(30): Show | 33 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.28-2943G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80205996 | ||||||
| chr5:80206053
|
A | G | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.28-3000T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80206053 | ||||||
| chr5:80206104
|
C | T | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.28-3051G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80206104 | ||||||
| chr5:80206260
|
A | G | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.28-3207T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80206260 | ||||||
| chr5:80206285
|
C | T | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.28-3232G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80206285 | ||||||
| chr5:80206449
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.28-3396T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80206449 | ||||||
| chr5:80206494
|
C | T | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.28-3441G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80206494 | ||||||
| chr5:80206811
|
C | CT | 131 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(128): Show | 131 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.28-3759dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80206811 | ||||||
| chr5:80206811
|
C | CTT | 81 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(78): Show | 81 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.28-3760_28-3759dup others(2): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80206811 | ||||||
| chr5:80206811
|
C | CTTT | 6 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0092others(3): Show | 6 | HG00438.hp2 HG01993.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-3761_28-3759dup others(3): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80206811 | ||||||
| chr5:80206831
|
A | G | 114 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(111): Show | 114 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.28-3778T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80206831 | ||||||
| chr5:80206847
|
T | C | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.28-3794A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80206847 | ||||||
| chr5:80206906
|
T | C | 1 | a0001c0001t0004g0171 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.28-3853A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80206906 | ||||||
| chr5:80206911
|
G | A | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.28-3858C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80206911 | ||||||
| chr5:80206995
|
C | CTA | 5 | a0001c0001t0006g0114a0001c0001t0006g0178a0001c0001t0013g0140others(2): Show | 5 | HG00741.hp1 HG01167.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-3944_28-3943dup others(2): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80206995 | ||||||
| chr5:80206995
|
C | CTATA | 4 | a0001c0001t0008g0259a0001c0001t0030g0255a0001c0001t0030g0257others(1): Show | 4 | HG02486.hp2 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-3946_28-3943dup others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80206995 | ||||||
| chr5:80207011
|
A | T | 5 | a0001c0001t0013g0068a0001c0001t0044g0149a0001c0001t0050g0265others(2): Show | 5 | HG00438.hp1 HG00609.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-3958T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80207011 | ||||||
| chr5:80207013
|
T | A | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.28-3960A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80207013 | ||||||
| chr5:80207102
|
C | A | 1 | a0001c0001t0006g0064 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.28-4049G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80207102 | ||||||
| chr5:80207117
|
GCCTCCCG others(7): Show |
G | 1 | a0001c0001t0010g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.28-4078_28-4065del others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80207117 | ||||||
| chr5:80207243
|
C | T | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.28-4190G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80207243 | ||||||
| chr5:80207244
|
G | A | 6 | a0001c0001t0013g0068a0001c0001t0044g0149a0001c0001t0046g0260others(3): Show | 6 | HG02257.hp1 HG02895.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-4191C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80207244 | ||||||
| chr5:80207384
|
C | T | 2 | a0001c0001t0001g0107a0001c0002t0003g0106 | 2 | NA18977.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.28-4331G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80207384 | ||||||
| chr5:80207472
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.28-4419G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80207472 | ||||||
| chr5:80207518
|
C | T | 10 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(7): Show | 10 | HG00140.hp1 HG00642.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.28-4465G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80207518 | ||||||
| chr5:80207532
|
T | A | 114 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(111): Show | 114 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.28-4479A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80207532 | ||||||
| chr5:80207629
|
T | C | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.28-4576A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80207629 | ||||||
| chr5:80207792
|
T | C | 35 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0002g0094others(32): Show | 35 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.28-4739A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80207792 | ||||||
| chr5:80207846
|
G | A | 2 | a0001c0006t0020g0127a0001c0006t0045g0128 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.28-4793C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80207846 | ||||||
| chr5:80207928
|
T | C | 10 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(7): Show | 10 | HG00140.hp1 HG00642.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.28-4875A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80207928 | ||||||
| chr5:80208023
|
C | T | 35 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0002g0094others(32): Show | 35 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.28-4970G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208023 | ||||||
| chr5:80208050
|
T | C | 17 | a0001c0001t0001g0151a0001c0001t0001g0269a0001c0001t0002g0109others(14): Show | 17 | HG01891.hp2 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.28-4997A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208050 | ||||||
| chr5:80208058
|
C | T | 2 | a0002c0005t0019g0042a0002c0005t0019g0273 | 2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.28-5005G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208058 | ||||||
| chr5:80208155
|
A | C | 2 | a0001c0001t0004g0154a0001c0001t0004g0203 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.28-5102T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208155 | ||||||
| chr5:80208192
|
A | C | 1 | a0001c0001t0015g0256 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.28-5139T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208192 | ||||||
| chr5:80208371
|
T | TA | 6 | a0001c0001t0001g0103a0001c0001t0002g0018a0001c0001t0002g0104others(3): Show | 6 | HG00140.hp2 HG00609.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-5319dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208371 | ||||||
| chr5:80208371
|
TA | T | 157 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0028others(154): Show | 157 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.28-5319delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208371 | ||||||
| chr5:80208371
|
TAA | T | 12 | a0001c0001t0001g0121a0001c0001t0001g0133a0001c0001t0002g0115others(9): Show | 12 | HG00140.hp1 HG00642.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.28-5320_28-5319del others(2): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208371 | ||||||
| chr5:80208393
|
C | A | 16 | a0001c0001t0007g0069a0001c0001t0007g0275a0001c0001t0008g0182others(13): Show | 16 | HG01167.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-5340G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208393 | ||||||
| chr5:80208439
|
GC | G | 37 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0002g0094others(34): Show | 37 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.28-5387delG | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208439 | ||||||
| chr5:80208445
|
C | G | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-5392G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208445 | ||||||
| chr5:80208446
|
C | A | 5 | a0001c0001t0007g0069a0001c0001t0007g0275a0001c0001t0008g0182others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-5393G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208446 | ||||||
| chr5:80208471
|
G | A | 5 | a0001c0001t0007g0069a0001c0001t0007g0275a0001c0001t0008g0182others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-5418C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208471 | ||||||
| chr5:80208492
|
T | C | 5 | a0001c0001t0007g0069a0001c0001t0007g0275a0001c0001t0008g0182others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-5439A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208492 | ||||||
| chr5:80208517
|
C | G | 32 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0002g0094others(29): Show | 32 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.28-5464G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208517 | ||||||
| chr5:80208556
|
T | G | 3 | a0001c0001t0001g0269a0001c0001t0002g0270a0001c0001t0002g0280 | 3 | HG02896.hp2 HG02897.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.28-5503A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208556 | ||||||
| chr5:80208652
|
A | G | 1 | a0001c0001t0041g0279 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.28-5599T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208652 | ||||||
| chr5:80208668
|
G | A | 35 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0002g0094others(32): Show | 35 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.28-5615C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208668 | ||||||
| chr5:80208870
|
G | A | 10 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(7): Show | 10 | HG00140.hp1 HG00642.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.28-5817C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208870 | ||||||
| chr5:80208960
|
T | C | 36 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0002g0094others(33): Show | 36 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.28-5907A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80208960 | ||||||
| chr5:80209012
|
T | C | 6 | a0001c0001t0013g0068a0001c0001t0044g0149a0001c0001t0046g0260others(3): Show | 6 | HG02257.hp1 HG02895.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-5959A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80209012 | ||||||
| chr5:80209040
|
C | T | 204 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0028others(201): Show | 204 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.28-5987G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80209040 | ||||||
| chr5:80209059
|
C | A | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.28-6006G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80209059 | ||||||
| chr5:80209087
|
A | G | 1 | a0001c0001t0021g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28-6034T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80209087 | ||||||
| chr5:80209105
|
T | C | 20 | a0001c0001t0001g0043a0001c0001t0002g0047a0001c0001t0002g0097others(17): Show | 20 | HG00735.hp2 HG01074.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.28-6052A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80209105 | ||||||
| chr5:80209113
|
A | G | 3 | a0001c0001t0002g0219a0001c0001t0004g0073a0001c0001t0004g0221 | 3 | HG02071.hp1 NA19074.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.28-6060T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80209113 | ||||||
| chr5:80209163
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0014g0152a0001c0001t0024g0165others(1): Show | 4 | NA18747.hp2 NA18948.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-6110C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80209163 | ||||||
| chr5:80209274
|
G | A | 1 | a0001c0001t0012g0251 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.28-6221C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80209274 | ||||||
| chr5:80209349
|
G | A | 2 | a0001c0001t0004g0282a0001c0001t0062g0283 | 2 | HG01943.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.28-6296C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80209349 | ||||||
| chr5:80209350
|
G | GAC | 37 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0002g0094others(34): Show | 37 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.28-6299_28-6298dup others(2): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80209350 | ||||||
| chr5:80209449
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.28-6396G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80209449 | ||||||
| chr5:80209599
|
C | T | 1 | a0001c0001t0010g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.28-6546G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80209599 | ||||||
| chr5:80209764
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0181 | 2 | NA18977.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.28-6711C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80209764 | ||||||
| chr5:80209793
|
A | C | 37 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0225others(34): Show | 37 | HG00408.hp2 HG00733.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.28-6740T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80209793 | ||||||
| chr5:80209986
|
G | A | 201 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(198): Show | 201 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.28-6933C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80209986 | ||||||
| chr5:80210049
|
A | G | 116 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(113): Show | 116 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.28-6996T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80210049 | ||||||
| chr5:80210060
|
G | GAAATA | 199 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(196): Show | 199 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.28-7012_28-7008dup others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80210060 | ||||||
| chr5:80210062
|
A | T | 1 | a0001c0001t0001g0006 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.28-7009T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80210062 | ||||||
| chr5:80210148
|
T | C | 8 | a0001c0001t0007g0275a0001c0001t0008g0182a0001c0001t0008g0240others(5): Show | 8 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-7095A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80210148 | ||||||
| chr5:80210166
|
C | T | 2 | a0001c0001t0001g0271a0001c0002t0073g0204 | 2 | HG01070.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.28-7113G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80210166 | ||||||
| chr5:80210167
|
G | A | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.28-7114C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80210167 | ||||||
| chr5:80210177
|
T | C | 50 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0039others(47): Show | 50 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.28-7124A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80210177 | ||||||
| chr5:80210238
|
G | A | 12 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(9): Show | 12 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.28-7185C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80210238 | ||||||
| chr5:80210297
|
T | C | 1 | a0001c0001t0010g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.28-7244A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80210297 | ||||||
| chr5:80210300
|
G | A | 1 | a0002c0003t0009g0228 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.28-7247C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80210300 | ||||||
| chr5:80210565
|
A | C | 1 | a0001c0001t0001g0045 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.28-7512T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80210565 | ||||||
| chr5:80210599
|
C | A | 1 | a0001c0002t0003g0082 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.28-7546G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80210599 | ||||||
| chr5:80210874
|
T | C | 9 | a0001c0001t0013g0068a0001c0001t0013g0140a0001c0001t0021g0141others(6): Show | 9 | HG01167.hp2 HG02895.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.28-7821A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80210874 | ||||||
| chr5:80210901
|
G | A | 2 | a0001c0001t0001g0271a0001c0002t0073g0204 | 2 | HG01070.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.28-7848C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80210901 | ||||||
| chr5:80211003
|
G | A | 7 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0069others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-7950C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80211003 | ||||||
| chr5:80211154
|
A | C | 86 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(83): Show | 86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.28-8101T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80211154 | ||||||
| chr5:80211334
|
A | G | 1 | a0001c0001t0065g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.28-8281T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80211334 | ||||||
| chr5:80211375
|
G | A | 53 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0133others(50): Show | 53 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.28-8322C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80211375 | ||||||
| chr5:80211395
|
GT | G | 204 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.28-8343delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80211395 | ||||||
| chr5:80211594
|
T | A | 1 | a0001c0002t0016g0033 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.28-8541A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80211594 | ||||||
| chr5:80211688
|
T | C | 1 | a0001c0009t0035g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.28-8635A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80211688 | ||||||
| chr5:80211807
|
G | A | 1 | a0001c0002t0003g0041 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.28-8754C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80211807 | ||||||
| chr5:80212025
|
G | A | 2 | a0001c0001t0038g0111a0002c0003t0009g0228 | 2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28-8972C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212025 | ||||||
| chr5:80212167
|
G | T | 8 | a0001c0001t0007g0275a0001c0001t0008g0182a0001c0001t0008g0240others(5): Show | 8 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-9114C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212167 | ||||||
| chr5:80212168
|
T | C | 8 | a0001c0001t0007g0275a0001c0001t0008g0182a0001c0001t0008g0240others(5): Show | 8 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-9115A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212168 | ||||||
| chr5:80212194
|
C | A | 26 | a0001c0001t0001g0043a0001c0001t0002g0047a0001c0001t0002g0097others(23): Show | 26 | HG00735.hp2 HG01074.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.28-9141G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212194 | ||||||
| chr5:80212217
|
G | A | 4 | a0001c0001t0013g0140a0001c0001t0047g0261a0002c0005t0019g0042others(1): Show | 4 | HG01167.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-9164C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212217 | ||||||
| chr5:80212256
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.28-9203T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212256 | ||||||
| chr5:80212425
|
C | T | 15 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(12): Show | 15 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.28-9372G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212425 | ||||||
| chr5:80212433
|
G | A | 32 | a0001c0001t0001g0151a0001c0001t0001g0269a0001c0001t0002g0109others(29): Show | 32 | HG00741.hp2 HG01109.hp2 HG01515.hp1 others(29): Show |
intron_variant | MODIFIER | c.28-9380C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212433 | ||||||
| chr5:80212509
|
A | C | 1 | a0001c0001t0065g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.28-9456T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212509 | ||||||
| chr5:80212565
|
C | T | 2 | a0001c0006t0020g0127a0001c0006t0045g0128 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.28-9512G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212565 | ||||||
| chr5:80212662
|
GGGT | G | 23 | a0001c0001t0001g0043a0001c0001t0002g0047a0001c0001t0002g0097others(20): Show | 23 | HG00735.hp2 HG01074.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.28-9612_28-9610del others(3): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212662 | ||||||
| chr5:80212663
|
GGT | G | 69 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0028others(66): Show | 69 | HG00408.hp1 HG00438.hp2 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.28-9612_28-9611del others(2): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212663 | ||||||
| chr5:80212664
|
GT | G | 13 | a0001c0001t0001g0029a0001c0001t0002g0156a0001c0001t0002g0197others(10): Show | 13 | HG01071.hp2 HG01169.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.28-9612delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212664 | ||||||
| chr5:80212665
|
T | G | 5 | a0001c0001t0007g0142a0001c0001t0033g0060a0001c0001t0059g0059others(2): Show | 5 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-9612A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212665 | ||||||
| chr5:80212668
|
G | C | 2 | a0001c0002t0003g0085a0001c0002t0003g0087 | 2 | HG00438.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.28-9615C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212668 | ||||||
| chr5:80212670
|
G | GGA | 18 | a0001c0001t0001g0151a0001c0001t0001g0269a0001c0001t0002g0109others(15): Show | 18 | HG00741.hp2 HG01891.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.28-9618_28-9617ins others(2): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212670 | ||||||
| chr5:80212672
|
G | T | 17 | a0001c0001t0001g0043a0001c0001t0002g0047a0001c0001t0002g0097others(14): Show | 17 | HG00735.hp2 HG01074.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.28-9619C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212672 | ||||||
| chr5:80212844
|
A | G | 2 | a0001c0001t0038g0111a0002c0003t0009g0228 | 2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28-9791T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212844 | ||||||
| chr5:80212884
|
C | T | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.28-9831G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212884 | ||||||
| chr5:80212954
|
T | C | 4 | a0001c0001t0001g0029a0001c0001t0014g0152a0001c0001t0024g0165others(1): Show | 4 | NA18747.hp2 NA18948.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-9901A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80212954 | ||||||
| chr5:80213200
|
C | T | 117 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0028others(114): Show | 117 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(114): Show |
intron_variant | MODIFIER | c.28-10147G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80213200 | ||||||
| chr5:80213210
|
T | G | 4 | a0001c0001t0013g0140a0001c0001t0047g0261a0002c0005t0019g0042others(1): Show | 4 | HG01167.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-10157A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80213210 | ||||||
| chr5:80213245
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0043a0001c0002t0003g0205 | 2 | HG02027.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.28-10193_28-10192i others(16): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80213245 | ||||||
| chr5:80213245
|
C | CAAAAAAA others(8): Show |
53 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0166others(50): Show | 53 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.28-10193_28-10192i others(17): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80213245 | ||||||
| chr5:80213245
|
C | CAAAAAAA others(9): Show |
105 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(102): Show | 105 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.28-10193_28-10192i others(18): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80213245 | ||||||
| chr5:80213245
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0028g0160a0001c0001t0037g0262 | 2 | HG03490.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.28-10193_28-10192i others(19): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80213245 | ||||||
| chr5:80213245
|
C | CAAAAAAA others(9): Show |
15 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(12): Show | 15 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.28-10193_28-10192i others(18): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80213245 | ||||||
| chr5:80213245
|
C | CAAAAAAA others(8): Show |
33 | a0001c0001t0001g0151a0001c0001t0001g0269a0001c0001t0002g0109others(30): Show | 33 | HG00741.hp2 HG01109.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.28-10193_28-10192i others(17): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80213245 | ||||||
| chr5:80213245
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0063g0164 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.28-10193_28-10192i others(16): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80213245 | ||||||
| chr5:80213326
|
A | G | 1 | a0001c0001t0002g0109 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.28-10273T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80213326 | ||||||
| chr5:80213386
|
C | A | 1 | a0001c0002t0003g0106 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.28-10333G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80213386 | ||||||
| chr5:80213436
|
G | A | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.28-10383C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80213436 | ||||||
| chr5:80213476
|
C | T | 27 | a0001c0001t0001g0043a0001c0001t0002g0047a0001c0001t0002g0097others(24): Show | 27 | HG00735.hp2 HG01074.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.28-10423G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80213476 | ||||||
| chr5:80213615
|
C | T | 1 | a0001c0002t0016g0034 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.28-10562G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80213615 | ||||||
| chr5:80213846
|
A | T | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.28-10793T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80213846 | ||||||
| chr5:80213907
|
G | A | 1 | a0002c0003t0009g0228 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.28-10854C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80213907 | ||||||
| chr5:80214072
|
A | G | 204 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.28-11019T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214072 | ||||||
| chr5:80214155
|
G | A | 116 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(113): Show | 116 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.28-11102C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214155 | ||||||
| chr5:80214173
|
G | A | 20 | a0001c0001t0001g0043a0001c0001t0002g0047a0001c0001t0002g0097others(17): Show | 20 | HG00735.hp2 HG01074.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.28-11120C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214173 | ||||||
| chr5:80214366
|
A | G | 2 | a0001c0006t0020g0127a0001c0006t0045g0128 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.28-11313T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214366 | ||||||
| chr5:80214374
|
T | G | 1 | a0001c0001t0001g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.28-11321A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214374 | ||||||
| chr5:80214538
|
C | T | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.28-11485G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214538 | ||||||
| chr5:80214552
|
T | TA | 62 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(59): Show | 62 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.28-11500dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214552 | ||||||
| chr5:80214559
|
A | G | 1 | a0002c0004t0005g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.28-11506T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214559 | ||||||
| chr5:80214560
|
C | A | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.28-11507G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214560 | ||||||
| chr5:80214560
|
C | CA | 128 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(125): Show | 128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.28-11508dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214560 | ||||||
| chr5:80214568
|
A | AAAT | 61 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(58): Show | 61 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.28-11516_28-11515i others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214568 | ||||||
| chr5:80214572
|
G | A | 64 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.28-11519C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214572 | ||||||
| chr5:80214594
|
C | T | 1 | a0004c0008t0001g0008 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.28-11541G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214594 | ||||||
| chr5:80214627
|
T | C | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-11574A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214627 | ||||||
| chr5:80214651
|
C | T | 64 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.28-11598G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214651 | ||||||
| chr5:80214686
|
T | C | 64 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.28-11633A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214686 | ||||||
| chr5:80214691
|
G | A | 64 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.28-11638C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214691 | ||||||
| chr5:80214879
|
G | A | 111 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0028others(108): Show | 111 | HG00408.hp1 HG00438.hp2 HG00735.hp2 others(108): Show |
intron_variant | MODIFIER | c.28-11826C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214879 | ||||||
| chr5:80214883
|
C | G | 64 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.28-11830G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214883 | ||||||
| chr5:80214894
|
T | C | 15 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(12): Show | 15 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.28-11841A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214894 | ||||||
| chr5:80214983
|
A | T | 187 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(184): Show | 187 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.28-11930T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80214983 | ||||||
| chr5:80215004
|
T | C | 1 | a0001c0002t0031g0001 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.28-11951A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80215004 | ||||||
| chr5:80215148
|
A | G | 64 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.28-12095T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80215148 | ||||||
| chr5:80215216
|
A | ACAGGGAG others(3): Show |
1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.28-12173_28-12164d others(12): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80215216 | ||||||
| chr5:80215269
|
A | T | 2 | a0001c0001t0038g0111a0002c0003t0009g0228 | 2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28-12216T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80215269 | ||||||
| chr5:80215270
|
C | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0218 | 2 | HG02040.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.28-12217G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80215270 | ||||||
| chr5:80215440
|
T | C | 64 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.28-12387A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80215440 | ||||||
| chr5:80215463
|
T | C | 64 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.28-12410A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80215463 | ||||||
| chr5:80215609
|
C | T | 1 | a0001c0001t0041g0279 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.28-12556G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80215609 | ||||||
| chr5:80215650
|
T | G | 64 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.28-12597A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80215650 | ||||||
| chr5:80215653
|
T | G | 64 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.28-12600A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80215653 | ||||||
| chr5:80215718
|
C | T | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.28-12665G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80215718 | ||||||
| chr5:80215719
|
G | A | 2 | a0001c0006t0020g0127a0001c0006t0045g0128 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.28-12666C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80215719 | ||||||
| chr5:80215827
|
C | T | 111 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0028others(108): Show | 111 | HG00408.hp1 HG00438.hp2 HG00735.hp2 others(108): Show |
intron_variant | MODIFIER | c.28-12774G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80215827 | ||||||
| chr5:80215828
|
G | A | 1 | a0001c0001t0046g0260 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.28-12775C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80215828 | ||||||
| chr5:80215862
|
G | A | 204 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.28-12809C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80215862 | ||||||
| chr5:80215911
|
G | A | 1 | a0001c0001t0004g0247 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.28-12858C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80215911 | ||||||
| chr5:80216034
|
A | G | 64 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.28-12981T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80216034 | ||||||
| chr5:80216035
|
T | G | 64 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.28-12982A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80216035 | ||||||
| chr5:80216060
|
G | C | 2 | a0001c0006t0020g0127a0001c0006t0045g0128 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.28-13007C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80216060 | ||||||
| chr5:80216101
|
A | T | 2 | a0001c0001t0013g0140a0001c0001t0047g0261 | 2 | HG01167.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.28-13048T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80216101 | ||||||
| chr5:80216174
|
C | G | 3 | a0001c0001t0013g0068a0001c0001t0044g0149a0001c0001t0050g0265 | 3 | HG02895.hp1 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.28-13121G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80216174 | ||||||
| chr5:80216203
|
C | A | 1 | a0001c0001t0015g0063 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.28-13150G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80216203 | ||||||
| chr5:80216449
|
A | C | 7 | a0001c0001t0007g0275a0001c0001t0008g0182a0001c0001t0008g0240others(4): Show | 7 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-13396T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80216449 | ||||||
| chr5:80216487
|
C | T | 29 | a0001c0001t0001g0043a0001c0001t0002g0047a0001c0001t0002g0097others(26): Show | 29 | HG00735.hp2 HG01074.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.28-13434G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80216487 | ||||||
| chr5:80216489
|
G | A | 15 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(12): Show | 15 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.28-13436C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80216489 | ||||||
| chr5:80216533
|
G | A | 64 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(61): Show | 64 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.28-13480C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80216533 | ||||||
| chr5:80216664
|
T | G | 204 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.28-13611A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80216664 | ||||||
| chr5:80216683
|
A | G | 65 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(62): Show | 65 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.28-13630T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80216683 | ||||||
| chr5:80216707
|
A | AT | 29 | a0001c0001t0001g0043a0001c0001t0002g0047a0001c0001t0002g0097others(26): Show | 29 | HG00735.hp2 HG01074.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.28-13655dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80216707 | ||||||
| chr5:80216798
|
T | C | 66 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(63): Show | 66 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.28-13745A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80216798 | ||||||
| chr5:80216837
|
A | G | 1 | a0001c0002t0016g0034 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.28-13784T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80216837 | ||||||
| chr5:80217045
|
T | G | 6 | a0001c0001t0001g0103a0001c0001t0002g0104a0001c0001t0004g0229others(3): Show | 6 | HG00609.hp2 HG02129.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-13992A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80217045 | ||||||
| chr5:80217104
|
ATTT | A | 50 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(47): Show | 50 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.28-14054_28-14052d others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80217104 | ||||||
| chr5:80217135
|
A | G | 1 | a0001c0001t0011g0009 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.28-14082T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80217135 | ||||||
| chr5:80217186
|
T | TAA | 65 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(62): Show | 65 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.28-14134_28-14133i others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80217186 | ||||||
| chr5:80217233
|
C | T | 65 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(62): Show | 65 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.28-14180G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80217233 | ||||||
| chr5:80217235
|
G | A | 2 | a0001c0001t0033g0060a0001c0002t0022g0272 | 2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.28-14182C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80217235 | ||||||
| chr5:80217242
|
C | G | 1 | a0001c0010t0005g0223 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.28-14189G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80217242 | ||||||
| chr5:80217248
|
T | C | 15 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(12): Show | 15 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.28-14195A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80217248 | ||||||
| chr5:80217585
|
C | T | 3 | a0001c0001t0004g0154a0001c0001t0004g0203a0001c0001t0057g0196 | 3 | HG01069.hp1 HG01071.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.28-14532G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80217585 | ||||||
| chr5:80218081
|
C | T | 3 | a0001c0001t0002g0163a0001c0001t0063g0164a0001c0002t0031g0001 | 3 | HG01109.hp2 HG01515.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.28-15028G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80218081 | ||||||
| chr5:80218203
|
C | T | 88 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0133others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.28-15150G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80218203 | ||||||
| chr5:80218412
|
T | C | 1 | a0001c0009t0035g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.28-15359A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80218412 | ||||||
| chr5:80218474
|
A | G | 1 | a0001c0001t0007g0142 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.28-15421T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80218474 | ||||||
| chr5:80218512
|
C | G | 65 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(62): Show | 65 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.28-15459G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80218512 | ||||||
| chr5:80218548
|
G | A | 65 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0151others(62): Show | 65 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.28-15495C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80218548 | ||||||
| chr5:80218624
|
G | A | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.28-15571C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80218624 | ||||||
| chr5:80218673
|
C | CA | 10 | a0001c0001t0001g0268a0001c0001t0002g0093a0001c0001t0008g0267others(7): Show | 10 | HG00639.hp2 HG00642.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.28-15621dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80218673 | ||||||
| chr5:80218723
|
A | G | 3 | a0001c0001t0002g0169a0001c0001t0011g0123a0001c0001t0011g0245 | 3 | HG01106.hp1 HG02004.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.28-15670T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80218723 | ||||||
| chr5:80218744
|
T | C | 1 | a0001c0001t0004g0073 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.28-15691A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80218744 | ||||||
| chr5:80218758
|
C | T | 2 | a0001c0002t0068g0188a0001c0002t0070g0189 | 2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.28-15705G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80218758 | ||||||
| chr5:80218759
|
G | A | 3 | a0001c0001t0037g0262a0001c0006t0020g0127a0001c0006t0045g0128 | 3 | HG02451.hp2 HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.28-15706C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80218759 | ||||||
| chr5:80218798
|
G | A | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-15745C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80218798 | ||||||
| chr5:80218856
|
G | A | 205 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(202): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.28-15803C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80218856 | ||||||
| chr5:80218914
|
A | G | 205 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(202): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.28-15861T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80218914 | ||||||
| chr5:80218961
|
C | T | 2 | a0001c0001t0013g0140a0001c0001t0047g0261 | 2 | HG01167.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.28-15908G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80218961 | ||||||
| chr5:80219060
|
T | A | 7 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0069others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-16007A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80219060 | ||||||
| chr5:80219062
|
C | A | 7 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0069others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-16009G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80219062 | ||||||
| chr5:80219116
|
G | A | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-16063C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80219116 | ||||||
| chr5:80219469
|
C | T | 128 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(125): Show | 128 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.28-16416G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80219469 | ||||||
| chr5:80219496
|
C | T | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.28-16443G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80219496 | ||||||
| chr5:80219639
|
G | A | 1 | a0002c0003t0009g0228 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.28-16586C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80219639 | ||||||
| chr5:80219801
|
T | C | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.28-16748A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80219801 | ||||||
| chr5:80219833
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.28-16780G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80219833 | ||||||
| chr5:80219857
|
GT | G | 19 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(16): Show | 19 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.28-16805delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80219857 | ||||||
| chr5:80219974
|
G | A | 3 | a0001c0001t0020g0057a0001c0001t0059g0059a0001c0002t0005g0058 | 3 | HG01243.hp1 HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.28-16921C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80219974 | ||||||
| chr5:80220011
|
C | A | 1 | a0001c0006t0020g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.28-16958G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80220011 | ||||||
| chr5:80220064
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.28-17011G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80220064 | ||||||
| chr5:80220165
|
G | A | 2 | a0001c0006t0020g0127a0001c0006t0045g0128 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.28-17112C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80220165 | ||||||
| chr5:80220187
|
G | A | 21 | a0001c0001t0001g0043a0001c0001t0002g0047a0001c0001t0002g0093others(18): Show | 21 | HG00642.hp1 HG00735.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.28-17134C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80220187 | ||||||
| chr5:80220226
|
A | T | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.28-17173T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80220226 | ||||||
| chr5:80220231
|
AAGAG | A | 15 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(12): Show | 15 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.28-17182_28-17179d others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80220231 | ||||||
| chr5:80220232
|
AG | A | 174 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(171): Show | 174 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.28-17180delC | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80220232 | ||||||
| chr5:80220233
|
G | A | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.28-17180C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80220233 | ||||||
| chr5:80220255
|
T | C | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.28-17202A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80220255 | ||||||
| chr5:80220260
|
T | G | 4 | a0001c0001t0013g0068a0001c0001t0044g0149a0001c0001t0046g0260others(1): Show | 4 | HG02895.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-17207A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80220260 | ||||||
| chr5:80220318
|
T | C | 1 | a0001c0001t0004g0138 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.28-17265A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80220318 | ||||||
| chr5:80220439
|
G | T | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.28-17386C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80220439 | ||||||
| chr5:80220467
|
G | T | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.28-17414C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80220467 | ||||||
| chr5:80220631
|
G | A | 1 | a0001c0010t0005g0223 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.28-17578C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80220631 | ||||||
| chr5:80220669
|
C | G | 18 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(15): Show | 18 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.28-17616G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80220669 | ||||||
| chr5:80220757
|
T | C | 18 | a0001c0001t0001g0133a0001c0001t0001g0151a0001c0001t0002g0115others(15): Show | 18 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.28-17704A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80220757 | ||||||
| chr5:80220941
|
G | T | 2 | a0001c0001t0038g0111a0002c0003t0009g0228 | 2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28-17888C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80220941 | ||||||
| chr5:80221107
|
G | A | 54 | a0001c0001t0001g0039a0001c0001t0001g0151a0001c0001t0001g0225others(51): Show | 54 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.28-18054C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80221107 | ||||||
| chr5:80221246
|
A | G | 1 | a0001c0001t0002g0104 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.28-18193T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80221246 | ||||||
| chr5:80221277
|
G | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0225a0001c0001t0010g0183others(1): Show | 4 | HG02109.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-18224C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80221277 | ||||||
| chr5:80221343
|
G | A | 4 | a0001c0002t0003g0078a0001c0002t0003g0079a0001c0002t0003g0080others(1): Show | 4 | HG01255.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-18290C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80221343 | ||||||
| chr5:80221456
|
A | G | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-18403T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80221456 | ||||||
| chr5:80221493
|
A | C | 2 | a0001c0001t0038g0111a0002c0003t0009g0228 | 2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28-18440T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80221493 | ||||||
| chr5:80221508
|
CA | C | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-18456delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80221508 | ||||||
| chr5:80221553
|
G | C | 2 | a0001c0001t0009g0139a0001c0001t0021g0141 | 2 | HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.28-18500C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80221553 | ||||||
| chr5:80221760
|
T | C | 16 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-18707A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80221760 | ||||||
| chr5:80221769
|
A | G | 1 | a0001c0001t0001g0006 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.28-18716T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80221769 | ||||||
| chr5:80221792
|
C | CA | 159 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(156): Show | 159 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.28-18740dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80221792 | ||||||
| chr5:80221792
|
C | CAA | 9 | a0001c0001t0001g0268a0001c0001t0002g0163a0001c0001t0008g0267others(6): Show | 9 | HG00639.hp2 HG01106.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.28-18741_28-18740d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80221792 | ||||||
| chr5:80222047
|
C | T | 16 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-18994G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222047 | ||||||
| chr5:80222094
|
G | A | 1 | a0001c0001t0013g0140 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.28-19041C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222094 | ||||||
| chr5:80222111
|
A | G | 3 | a0001c0001t0002g0239a0001c0001t0002g0252a0001c0002t0005g0214 | 3 | NA18952.hp1 NA18971.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.28-19058T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222111 | ||||||
| chr5:80222260
|
G | A | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-19207C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222260 | ||||||
| chr5:80222358
|
C | G | 1 | a0001c0001t0006g0114 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.28-19305G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222358 | ||||||
| chr5:80222381
|
C | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(63): Show | 66 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.28-19328G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222381 | ||||||
| chr5:80222459
|
T | C | 179 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.28-19406A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222459 | ||||||
| chr5:80222468
|
C | T | 2 | a0002c0005t0019g0042a0002c0005t0019g0273 | 2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.28-19415G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222468 | ||||||
| chr5:80222479
|
C | CA | 16 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-19427dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222479 | ||||||
| chr5:80222549
|
G | GGTGAGTA others(1): Show |
4 | a0001c0001t0002g0219a0001c0001t0002g0239a0001c0001t0004g0073others(1): Show | 4 | HG02071.hp1 NA19074.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-19497_28-19496i others(10): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222549 | ||||||
| chr5:80222549
|
GGTGAGTG others(1): Show |
G | 8 | a0001c0001t0006g0114a0001c0001t0006g0173a0001c0001t0006g0174others(5): Show | 8 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-19504_28-19497d others(10): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222549 | ||||||
| chr5:80222553
|
A | AGTATGTG others(3): Show |
82 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(79): Show | 82 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.28-19501_28-19500i others(12): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222553 | ||||||
| chr5:80222553
|
A | AGTATGTG others(5): Show |
7 | a0001c0001t0002g0215a0001c0001t0004g0076a0001c0001t0004g0077others(4): Show | 7 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.28-19501_28-19500i others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222553 | ||||||
| chr5:80222556
|
G | A | 3 | a0001c0001t0002g0278a0001c0001t0021g0053a0001c0001t0061g0206 | 3 | HG02559.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.28-19503C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222556 | ||||||
| chr5:80222561
|
A | AGTGT | 4 | a0001c0001t0002g0278a0001c0001t0021g0053a0001c0002t0003g0090others(1): Show | 4 | HG00408.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-19512_28-19509d others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222561 | ||||||
| chr5:80222561
|
A | AGTGTGTG others(1): Show |
24 | a0001c0001t0001g0039a0001c0001t0001g0225a0001c0001t0002g0094others(21): Show | 24 | HG00621.hp1 HG00733.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.28-19509_28-19508i others(10): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222561 | ||||||
| chr5:80222561
|
A | AGTGTGTG others(3): Show |
7 | a0001c0001t0008g0240a0001c0001t0009g0139a0001c0001t0010g0235others(4): Show | 7 | HG01884.hp1 HG01934.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.28-19509_28-19508i others(12): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222561 | ||||||
| chr5:80222561
|
A | AGTGTGTG others(5): Show |
17 | a0001c0001t0007g0275a0001c0001t0007g0281a0001c0001t0008g0129others(14): Show | 17 | HG00741.hp2 HG01167.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.28-19509_28-19508i others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222561 | ||||||
| chr5:80222561
|
A | AGTGTGTG others(7): Show |
1 | a0001c0001t0002g0280 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.28-19509_28-19508i others(16): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222561 | ||||||
| chr5:80222561
|
A | AGTGTGTG others(9): Show |
9 | a0001c0001t0001g0151a0001c0001t0001g0269a0001c0001t0002g0270others(6): Show | 9 | HG02559.hp1 HG02895.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.28-19509_28-19508i others(18): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222561 | ||||||
| chr5:80222561
|
A | AGTGTGTG others(11): Show |
2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.28-19509_28-19508i others(20): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222561 | ||||||
| chr5:80222561
|
A | T | 94 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(91): Show | 94 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.28-19508T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222561 | ||||||
| chr5:80222567
|
TGA | T | 14 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.28-19516_28-19515d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222567 | ||||||
| chr5:80222569
|
A | AGT | 6 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(3): Show | 6 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-19518_28-19517d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222569 | ||||||
| chr5:80222569
|
A | T | 165 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(162): Show | 165 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.28-19516T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222569 | ||||||
| chr5:80222587
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0055g0276 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.28-19535_28-19534i others(13): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222587 | ||||||
| chr5:80222604
|
C | T | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-19551G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222604 | ||||||
| chr5:80222622
|
G | T | 101 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(98): Show | 101 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.28-19569C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222622 | ||||||
| chr5:80222630
|
T | C | 162 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(159): Show | 162 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.28-19577A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222630 | ||||||
| chr5:80222641
|
C | T | 16 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-19588G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222641 | ||||||
| chr5:80222673
|
A | G | 1 | a0001c0001t0051g0236 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.28-19620T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222673 | ||||||
| chr5:80222746
|
G | A | 179 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.28-19693C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222746 | ||||||
| chr5:80222784
|
G | A | 16 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-19731C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222784 | ||||||
| chr5:80222883
|
A | G | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-19830T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80222883 | ||||||
| chr5:80223150
|
C | G | 1 | a0001c0001t0041g0279 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.28-20097G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80223150 | ||||||
| chr5:80223202
|
A | T | 16 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-20149T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80223202 | ||||||
| chr5:80223223
|
T | C | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.28-20170A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80223223 | ||||||
| chr5:80223384
|
T | C | 12 | a0001c0001t0002g0109a0001c0001t0002g0280a0001c0001t0007g0281others(9): Show | 12 | HG00741.hp2 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.28-20331A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80223384 | ||||||
| chr5:80223491
|
C | T | 1 | a0001c0002t0005g0214 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.28-20438G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80223491 | ||||||
| chr5:80223736
|
T | C | 1 | a0001c0001t0039g0264 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.28-20683A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80223736 | ||||||
| chr5:80223783
|
T | G | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.28-20730A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80223783 | ||||||
| chr5:80223950
|
A | AC | 8 | a0001c0001t0002g0109a0001c0001t0002g0280a0001c0001t0007g0281others(5): Show | 8 | HG01891.hp2 HG02572.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-20898dupG | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80223950 | ||||||
| chr5:80223971
|
C | CA | 6 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(3): Show | 6 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-20919dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80223971 | ||||||
| chr5:80223993
|
C | T | 2 | a0001c0002t0005g0105a0001c0002t0005g0122 | 2 | NA18955.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.28-20940G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80223993 | ||||||
| chr5:80224002
|
G | A | 16 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-20949C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224002 | ||||||
| chr5:80224026
|
G | A | 2 | a0001c0002t0003g0085a0001c0002t0003g0087 | 2 | HG00438.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.28-20973C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224026 | ||||||
| chr5:80224133
|
C | CA | 78 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(75): Show | 78 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.28-21081dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224133 | ||||||
| chr5:80224133
|
C | CAA | 115 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(112): Show | 115 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.28-21082_28-21081d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224133 | ||||||
| chr5:80224133
|
C | CAAA | 6 | a0001c0001t0001g0092a0001c0001t0001g0107a0001c0001t0014g0152others(3): Show | 6 | HG03139.hp2 NA18747.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-21083_28-21081d others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224133 | ||||||
| chr5:80224133
|
CA | C | 16 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-21081delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224133 | ||||||
| chr5:80224292
|
A | T | 185 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.28-21239T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224292 | ||||||
| chr5:80224350
|
G | C | 4 | a0001c0001t0013g0068a0001c0001t0044g0149a0001c0001t0046g0260others(1): Show | 4 | HG02895.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-21297C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224350 | ||||||
| chr5:80224378
|
GAAGTGAG others(5): Show |
G | 16 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-21337_28-21326d others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224378 | ||||||
| chr5:80224383
|
G | A | 162 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(159): Show | 162 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.28-21330C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224383 | ||||||
| chr5:80224403
|
G | A | 6 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(3): Show | 6 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-21350C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224403 | ||||||
| chr5:80224409
|
C | T | 4 | a0001c0001t0013g0140a0001c0001t0047g0261a0001c0006t0020g0127others(1): Show | 4 | HG01167.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-21356G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224409 | ||||||
| chr5:80224421
|
G | A | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.28-21368C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224421 | ||||||
| chr5:80224713
|
A | T | 13 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.28-21660T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224713 | ||||||
| chr5:80224814
|
C | T | 163 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(160): Show | 163 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.28-21761G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224814 | ||||||
| chr5:80224835
|
G | A | 179 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.28-21782C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224835 | ||||||
| chr5:80224923
|
G | GT | 12 | a0001c0001t0001g0187a0001c0001t0001g0227a0001c0001t0001g0268others(9): Show | 12 | HG00639.hp2 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.28-21871dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224923 | ||||||
| chr5:80224923
|
GT | G | 19 | a0001c0001t0001g0092a0001c0001t0001g0100a0001c0001t0001g0218others(16): Show | 19 | HG00438.hp2 HG00621.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.28-21871delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224923 | ||||||
| chr5:80224923
|
GTT | G | 142 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(139): Show | 142 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.28-21872_28-21871d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224923 | ||||||
| chr5:80224926
|
TTTTTTTT others(2): Show |
T | 11 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0002g0134others(8): Show | 11 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-21882_28-21874d others(11): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224926 | ||||||
| chr5:80224936
|
T | G | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0037g0262others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-21883A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224936 | ||||||
| chr5:80224940
|
T | G | 163 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(160): Show | 163 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.28-21887A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224940 | ||||||
| chr5:80224941
|
T | G | 16 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-21888A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224941 | ||||||
| chr5:80224945
|
G | GT | 6 | a0001c0001t0001g0014a0001c0001t0004g0199a0001c0001t0025g0051others(3): Show | 6 | HG01361.hp1 HG01934.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-21893dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224945 | ||||||
| chr5:80224945
|
G | T | 6 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(3): Show | 6 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-21892C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224945 | ||||||
| chr5:80224945
|
GTTTTTT | G | 162 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(159): Show | 162 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.28-21898_28-21893d others(8): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224945 | ||||||
| chr5:80224949
|
T | G | 16 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-21896A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224949 | ||||||
| chr5:80224950
|
T | G | 1 | a0001c0001t0011g0009 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.28-21897A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224950 | ||||||
| chr5:80224953
|
T | G | 16 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-21900A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224953 | ||||||
| chr5:80224959
|
T | G | 179 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.28-21906A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224959 | ||||||
| chr5:80224974
|
C | T | 34 | a0001c0001t0001g0039a0001c0001t0001g0225a0001c0001t0002g0094others(31): Show | 34 | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.28-21921G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80224974 | ||||||
| chr5:80225001
|
C | T | 1 | a0001c0002t0003g0026 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.28-21948G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80225001 | ||||||
| chr5:80225156
|
G | A | 2 | a0001c0001t0038g0111a0002c0003t0009g0228 | 2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28-22103C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80225156 | ||||||
| chr5:80225171
|
C | G | 2 | a0001c0001t0001g0271a0001c0002t0073g0204 | 2 | HG01070.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.28-22118G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80225171 | ||||||
| chr5:80225265
|
C | G | 2 | a0001c0001t0007g0142a0001c0001t0058g0243 | 2 | HG01109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.28-22212G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80225265 | ||||||
| chr5:80225439
|
A | C | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.28-22386T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80225439 | ||||||
| chr5:80225687
|
A | G | 179 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.28-22634T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80225687 | ||||||
| chr5:80225724
|
C | T | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-22671G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80225724 | ||||||
| chr5:80225780
|
G | A | 179 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.28-22727C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80225780 | ||||||
| chr5:80225884
|
C | T | 2 | a0001c0001t0002g0219a0001c0001t0004g0221 | 2 | HG02071.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.28-22831G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80225884 | ||||||
| chr5:80225885
|
A | G | 163 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(160): Show | 163 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.28-22832T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80225885 | ||||||
| chr5:80225905
|
T | C | 179 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.28-22852A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80225905 | ||||||
| chr5:80225938
|
G | A | 20 | a0001c0001t0001g0043a0001c0001t0002g0047a0001c0001t0002g0093others(17): Show | 20 | HG00642.hp1 HG00735.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.28-22885C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80225938 | ||||||
| chr5:80225948
|
T | C | 97 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(94): Show | 97 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.28-22895A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80225948 | ||||||
| chr5:80226043
|
G | GA | 177 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(174): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.28-22991dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226043 | ||||||
| chr5:80226083
|
T | A | 2 | a0001c0001t0038g0111a0002c0003t0009g0228 | 2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28-23030A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226083 | ||||||
| chr5:80226105
|
T | C | 186 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(183): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.28-23052A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226105 | ||||||
| chr5:80226167
|
C | T | 2 | a0002c0004t0005g0110a0002c0004t0016g0231 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.28-23114G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226167 | ||||||
| chr5:80226184
|
A | T | 163 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(160): Show | 163 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.28-23131T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226184 | ||||||
| chr5:80226247
|
C | T | 163 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(160): Show | 163 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.28-23194G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226247 | ||||||
| chr5:80226268
|
G | T | 1 | a0001c0001t0021g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.28-23215C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226268 | ||||||
| chr5:80226373
|
G | A | 179 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.28-23320C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226373 | ||||||
| chr5:80226380
|
C | T | 16 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-23327G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226380 | ||||||
| chr5:80226468
|
T | C | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-23415A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226468 | ||||||
| chr5:80226578
|
G | C | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.28-23525C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226578 | ||||||
| chr5:80226590
|
T | C | 179 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.28-23537A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226590 | ||||||
| chr5:80226639
|
C | T | 185 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.28-23586G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226639 | ||||||
| chr5:80226678
|
C | T | 179 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.28-23625G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226678 | ||||||
| chr5:80226786
|
C | T | 20 | a0001c0001t0001g0043a0001c0001t0002g0047a0001c0001t0002g0093others(17): Show | 20 | HG00642.hp1 HG00735.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.28-23733G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226786 | ||||||
| chr5:80226801
|
G | A | 16 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-23748C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226801 | ||||||
| chr5:80226808
|
C | T | 179 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.28-23755G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226808 | ||||||
| chr5:80226876
|
A | T | 179 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.28-23823T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80226876 | ||||||
| chr5:80227040
|
T | C | 179 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.28-23987A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227040 | ||||||
| chr5:80227054
|
C | A | 97 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(94): Show | 97 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.28-24001G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227054 | ||||||
| chr5:80227086
|
A | G | 179 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.28-24033T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227086 | ||||||
| chr5:80227140
|
C | T | 101 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(98): Show | 101 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.28-24087G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227140 | ||||||
| chr5:80227201
|
C | T | 14 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.28-24148G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227201 | ||||||
| chr5:80227254
|
G | A | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-24201C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227254 | ||||||
| chr5:80227469
|
C | T | 2 | a0001c0001t0038g0111a0002c0003t0009g0228 | 2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28-24416G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227469 | ||||||
| chr5:80227549
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.28-24496G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227549 | ||||||
| chr5:80227559
|
G | A | 2 | a0001c0001t0013g0140a0001c0001t0047g0261 | 2 | HG01167.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.28-24506C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227559 | ||||||
| chr5:80227590
|
G | A | 2 | a0001c0001t0002g0112a0001c0001t0002g0113 | 2 | HG01099.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.28-24537C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227590 | ||||||
| chr5:80227606
|
C | CAAA | 13 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.28-24556_28-24554d others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227606 | ||||||
| chr5:80227619
|
AG | A | 129 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(126): Show | 129 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.28-24567delC | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227619 | ||||||
| chr5:80227620
|
G | A | 48 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0133others(45): Show | 48 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.28-24567C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227620 | ||||||
| chr5:80227624
|
C | T | 179 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.28-24571G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227624 | ||||||
| chr5:80227827
|
C | A | 2 | a0001c0001t0056g0198a0001c0002t0005g0038 | 2 | HG02040.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.28-24774G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227827 | ||||||
| chr5:80227886
|
A | C | 1 | a0001c0001t0002g0094 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.28-24833T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227886 | ||||||
| chr5:80227945
|
T | G | 177 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(174): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.28-24892A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227945 | ||||||
| chr5:80227971
|
CA | C | 16 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-24919delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80227971 | ||||||
| chr5:80228034
|
C | A | 16 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(13): Show | 16 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.28-24981G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80228034 | ||||||
| chr5:80228068
|
G | GA | 22 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(19): Show | 22 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.28-25016dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80228068 | ||||||
| chr5:80228261
|
A | AGGAAAGG others(18): Show |
1 | a0001c0002t0005g0201 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.28-25233_28-25209d others(27): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80228261 | ||||||
| chr5:80228274
|
G | GGGAGGGA others(6): Show |
1 | a0001c0001t0001g0153 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.28-25222_28-25221i others(15): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80228274 | ||||||
| chr5:80228310
|
G | A | 1 | a0001c0001t0002g0169 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.28-25257C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80228310 | ||||||
| chr5:80228459
|
A | AT | 170 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(167): Show | 170 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.28-25407dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80228459 | ||||||
| chr5:80228565
|
C | T | 1 | a0001c0001t0021g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.28-25512G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80228565 | ||||||
| chr5:80228722
|
C | T | 173 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(170): Show | 173 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.28-25669G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80228722 | ||||||
| chr5:80228778
|
C | A | 2 | a0001c0006t0020g0127a0001c0006t0045g0128 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.28-25725G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80228778 | ||||||
| chr5:80229021
|
C | CT | 19 | a0001c0001t0001g0089a0001c0001t0001g0107a0001c0001t0001g0177others(16): Show | 19 | HG00609.hp2 HG00741.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.28-25969dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229021 | ||||||
| chr5:80229021
|
CTTTTT | C | 14 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.28-25973_28-25969d others(7): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229021 | ||||||
| chr5:80229021
|
CTTTTTT | C | 6 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(3): Show | 6 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-25974_28-25969d others(8): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229021 | ||||||
| chr5:80229021
|
CTTTTTTT others(2): Show |
C | 17 | a0001c0001t0001g0166a0001c0001t0002g0024a0001c0001t0002g0211others(14): Show | 17 | HG00099.hp2 HG00609.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.28-25977_28-25969d others(11): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229021 | ||||||
| chr5:80229021
|
CTTTTTTT others(3): Show |
C | 58 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0029others(55): Show | 58 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.28-25978_28-25969d others(12): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229021 | ||||||
| chr5:80229021
|
CTTTTTTT others(4): Show |
C | 42 | a0001c0001t0001g0088a0001c0001t0001g0162a0001c0001t0002g0093others(39): Show | 42 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.28-25979_28-25969d others(13): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229021 | ||||||
| chr5:80229021
|
CTTTTTTT others(5): Show |
C | 40 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0225others(37): Show | 40 | HG00408.hp2 HG00733.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.28-25980_28-25969d others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229021 | ||||||
| chr5:80229021
|
CTTTTTTT others(6): Show |
C | 12 | a0001c0001t0008g0125a0001c0001t0008g0240a0001c0001t0009g0139others(9): Show | 12 | HG01884.hp1 HG02040.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.28-25981_28-25969d others(15): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229021 | ||||||
| chr5:80229021
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.28-25982_28-25969d others(16): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229021 | ||||||
| chr5:80229039
|
T | G | 5 | a0001c0001t0001g0022a0001c0001t0002g0025a0001c0001t0054g0253others(2): Show | 5 | HG01993.hp2 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-25986A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229039 | ||||||
| chr5:80229040
|
T | G | 25 | a0001c0001t0001g0022a0001c0001t0001g0166a0001c0001t0002g0024others(22): Show | 25 | HG00099.hp2 HG00609.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.28-25987A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229040 | ||||||
| chr5:80229041
|
T | G | 78 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(75): Show | 78 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.28-25988A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229041 | ||||||
| chr5:80229042
|
T | G | 121 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(118): Show | 121 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.28-25989A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229042 | ||||||
| chr5:80229043
|
T | G | 123 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(120): Show | 123 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.28-25990A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229043 | ||||||
| chr5:80229044
|
T | G | 164 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(161): Show | 164 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.28-25991A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229044 | ||||||
| chr5:80229045
|
T | G | 174 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(171): Show | 174 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.28-25992A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229045 | ||||||
| chr5:80229046
|
T | G | 174 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(171): Show | 174 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.28-25993A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229046 | ||||||
| chr5:80229047
|
T | A | 2 | a0001c0006t0020g0127a0001c0006t0045g0128 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.28-25994A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229047 | ||||||
| chr5:80229047
|
T | G | 173 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(170): Show | 173 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.28-25994A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229047 | ||||||
| chr5:80229048
|
T | G | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(172): Show | 175 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.28-25995A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229048 | ||||||
| chr5:80229049
|
T | G | 176 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(173): Show | 176 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.28-25996A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229049 | ||||||
| chr5:80229050
|
T | C | 1 | a0001c0002t0003g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.28-25997A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229050 | ||||||
| chr5:80229050
|
T | G | 187 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.28-25997A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229050 | ||||||
| chr5:80229052
|
G | C | 1 | a0001c0001t0002g0136 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.28-25999C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229052 | ||||||
| chr5:80229127
|
G | A | 95 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(92): Show | 95 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.28-26074C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229127 | ||||||
| chr5:80229130
|
T | A | 1 | a0001c0001t0024g0165 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.28-26077A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229130 | ||||||
| chr5:80229145
|
T | C | 18 | a0001c0001t0001g0151a0001c0001t0001g0269a0001c0001t0002g0109others(15): Show | 18 | HG00741.hp2 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.28-26092A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229145 | ||||||
| chr5:80229184
|
C | G | 1 | a0001c0001t0032g0004 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.28-26131G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229184 | ||||||
| chr5:80229254
|
C | A | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(172): Show | 175 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.28-26201G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229254 | ||||||
| chr5:80229270
|
T | C | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(172): Show | 175 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.28-26217A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229270 | ||||||
| chr5:80229279
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.28-26226G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229279 | ||||||
| chr5:80229285
|
A | T | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(172): Show | 175 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.28-26232T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229285 | ||||||
| chr5:80229317
|
C | A | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.28-26264G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229317 | ||||||
| chr5:80229341
|
A | AT | 64 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(61): Show | 64 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.28-26289dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229341 | ||||||
| chr5:80229341
|
A | ATT | 62 | a0001c0001t0001g0100a0001c0001t0001g0151a0001c0001t0001g0213others(59): Show | 62 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.28-26290_28-26289d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229341 | ||||||
| chr5:80229341
|
A | ATTT | 13 | a0001c0001t0001g0039a0001c0001t0002g0280a0001c0001t0007g0281others(10): Show | 13 | HG01884.hp1 HG02523.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.28-26291_28-26289d others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229341 | ||||||
| chr5:80229341
|
A | ATTTT | 10 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(7): Show | 10 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.28-26292_28-26289d others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229341 | ||||||
| chr5:80229341
|
AT | A | 11 | a0001c0001t0001g0232a0001c0001t0002g0012a0001c0001t0004g0076others(8): Show | 11 | HG00408.hp1 HG00733.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-26289delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229341 | ||||||
| chr5:80229390
|
T | A | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(172): Show | 175 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.28-26337A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229390 | ||||||
| chr5:80229441
|
G | C | 3 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0026g0244 | 3 | HG00140.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.28-26388C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229441 | ||||||
| chr5:80229486
|
A | G | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(172): Show | 175 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.27+26410T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229486 | ||||||
| chr5:80229545
|
A | G | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(172): Show | 175 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.27+26351T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229545 | ||||||
| chr5:80229549
|
A | C | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(172): Show | 175 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.27+26347T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229549 | ||||||
| chr5:80229641
|
G | GA | 173 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(170): Show | 173 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.27+26254dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229641 | ||||||
| chr5:80229750
|
G | A | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(172): Show | 175 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.27+26146C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229750 | ||||||
| chr5:80229758
|
T | G | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.27+26138A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229758 | ||||||
| chr5:80229764
|
T | G | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.27+26132A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229764 | ||||||
| chr5:80229778
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.27+26118A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229778 | ||||||
| chr5:80229859
|
T | C | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.27+26037A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229859 | ||||||
| chr5:80229898
|
C | T | 13 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.27+25998G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80229898 | ||||||
| chr5:80230185
|
T | A | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.27+25711A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230185 | ||||||
| chr5:80230193
|
A | G | 174 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(171): Show | 174 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.27+25703T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230193 | ||||||
| chr5:80230301
|
A | T | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(172): Show | 175 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.27+25595T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230301 | ||||||
| chr5:80230339
|
T | C | 119 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(116): Show | 119 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.27+25557A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230339 | ||||||
| chr5:80230365
|
T | C | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(172): Show | 175 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.27+25531A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230365 | ||||||
| chr5:80230390
|
G | A | 1 | a0001c0001t0010g0235 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.27+25506C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230390 | ||||||
| chr5:80230445
|
CA | C | 109 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.27+25450delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230445 | ||||||
| chr5:80230459
|
A | AAAAAAAA others(8): Show |
1 | a0002c0005t0019g0273 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.27+25436_27+25437i others(17): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230459 | ||||||
| chr5:80230459
|
A | AAAAAAAA others(7): Show |
1 | a0002c0005t0019g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.27+25436_27+25437i others(16): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230459 | ||||||
| chr5:80230459
|
A | AAAAAAAA others(5): Show |
3 | a0001c0001t0042g0065a0001c0006t0020g0127a0001c0006t0045g0128 | 3 | HG02451.hp2 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.27+25436_27+25437i others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230459 | ||||||
| chr5:80230459
|
A | AAAAAAAA others(4): Show |
8 | a0001c0001t0002g0277a0001c0001t0004g0138a0001c0001t0006g0064others(5): Show | 8 | HG01243.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.27+25436_27+25437i others(13): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230459 | ||||||
| chr5:80230459
|
A | AAAAAAAA others(3): Show |
31 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0153others(28): Show | 31 | HG00099.hp2 HG00642.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.27+25436_27+25437i others(12): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230459 | ||||||
| chr5:80230459
|
A | AAAAAAAA others(2): Show |
66 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(63): Show | 66 | HG01099.hp1 HG01168.hp1 HG01169.hp1 others(63): Show |
intron_variant | MODIFIER | c.27+25436_27+25437i others(11): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230459 | ||||||
| chr5:80230459
|
A | AAAAAAAA others(1): Show |
60 | a0001c0001t0001g0039a0001c0001t0001g0100a0001c0001t0001g0151others(57): Show | 60 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.27+25436_27+25437i others(10): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230459 | ||||||
| chr5:80230459
|
A | G | 1 | a0002c0003t0009g0228 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.27+25437T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230459 | ||||||
| chr5:80230473
|
C | T | 94 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(91): Show | 94 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.27+25423G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230473 | ||||||
| chr5:80230479
|
A | G | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(172): Show | 175 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.27+25417T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230479 | ||||||
| chr5:80230504
|
C | A | 2 | a0001c0002t0005g0105a0001c0002t0005g0122 | 2 | NA18955.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.27+25392G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230504 | ||||||
| chr5:80230527
|
G | A | 64 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(61): Show | 64 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.27+25369C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230527 | ||||||
| chr5:80230549
|
CAAAT | C | 30 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0002g0047others(27): Show | 30 | HG00642.hp1 HG00735.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.27+25343_27+25346d others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230549 | ||||||
| chr5:80230571
|
C | A | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(172): Show | 175 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.27+25325G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230571 | ||||||
| chr5:80230637
|
C | A | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.27+25259G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230637 | ||||||
| chr5:80230779
|
CTCTT | C | 123 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(120): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.27+25113_27+25116d others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230779 | ||||||
| chr5:80230795
|
TTC | T | 55 | a0001c0001t0001g0039a0001c0001t0001g0151a0001c0001t0001g0225others(52): Show | 55 | HG00408.hp2 HG00733.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.27+25099_27+25100d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230795 | ||||||
| chr5:80230842
|
A | C | 2 | a0001c0001t0007g0142a0001c0001t0058g0243 | 2 | HG01109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.27+25054T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230842 | ||||||
| chr5:80230885
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.27+25011A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230885 | ||||||
| chr5:80230915
|
C | T | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(172): Show | 175 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.27+24981G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230915 | ||||||
| chr5:80230938
|
G | A | 2 | a0001c0002t0068g0188a0001c0002t0070g0189 | 2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.27+24958C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80230938 | ||||||
| chr5:80231012
|
C | CA | 175 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(172): Show | 175 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.27+24883_27+24884i others(3): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80231012 | ||||||
| chr5:80231182
|
A | G | 174 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(171): Show | 174 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.27+24714T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80231182 | ||||||
| chr5:80231203
|
C | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(10): Show | 13 | HG01496.hp2 HG01975.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.27+24693G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80231203 | ||||||
| chr5:80231267
|
C | T | 7 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0069others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+24629G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80231267 | ||||||
| chr5:80231268
|
G | A | 13 | a0001c0001t0001g0133a0001c0001t0002g0115a0001c0001t0002g0116others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.27+24628C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80231268 | ||||||
| chr5:80231433
|
C | A | 1 | a0001c0001t0002g0018 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.27+24463G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80231433 | ||||||
| chr5:80231436
|
C | T | 6 | a0001c0001t0001g0022a0001c0001t0002g0024a0001c0001t0002g0025others(3): Show | 6 | HG00099.hp2 HG01099.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.27+24460G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80231436 | ||||||
| chr5:80231446
|
T | C | 3 | a0001c0001t0020g0057a0001c0001t0059g0059a0001c0002t0005g0058 | 3 | HG01243.hp1 HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.27+24450A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80231446 | ||||||
| chr5:80231513
|
T | A | 1 | a0001c0001t0002g0136 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.27+24383A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80231513 | ||||||
| chr5:80231565
|
C | T | 1 | a0001c0001t0014g0086 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.27+24331G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80231565 | ||||||
| chr5:80231623
|
TA | T | 8 | a0001c0001t0001g0227a0001c0001t0002g0270a0001c0001t0002g0278others(5): Show | 8 | HG01243.hp1 HG01517.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.27+24272delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80231623 | ||||||
| chr5:80232101
|
TAA | T | 51 | a0001c0001t0001g0039a0001c0001t0001g0133a0001c0001t0001g0225others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.27+23793_27+23794d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232101 | ||||||
| chr5:80232101
|
TAAA | T | 30 | a0001c0001t0001g0269a0001c0001t0002g0109a0001c0001t0002g0248others(27): Show | 30 | HG00741.hp2 HG01243.hp2 HG01515.hp1 others(27): Show |
intron_variant | MODIFIER | c.27+23792_27+23794d others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232101 | ||||||
| chr5:80232101
|
TAAAA | T | 109 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(106): Show | 109 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.27+23791_27+23794d others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232101 | ||||||
| chr5:80232102
|
A | T | 2 | a0001c0001t0022g0185a0001c0002t0003g0184 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.27+23794T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232102 | ||||||
| chr5:80232127
|
G | A | 3 | a0001c0001t0013g0068a0001c0001t0044g0149a0001c0002t0027g0148 | 3 | HG01884.hp2 HG02895.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.27+23769C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232127 | ||||||
| chr5:80232131
|
A | G | 2 | a0001c0001t0023g0130a0001c0001t0037g0262 | 2 | HG03704.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.27+23765T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232131 | ||||||
| chr5:80232132
|
A | C | 2 | a0001c0001t0023g0130a0001c0001t0037g0262 | 2 | HG03704.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.27+23764T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232132 | ||||||
| chr5:80232133
|
G | A | 1 | a0001c0001t0023g0130 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.27+23763C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232133 | ||||||
| chr5:80232136
|
G | C | 1 | a0001c0001t0011g0245 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.27+23760C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232136 | ||||||
| chr5:80232140
|
C | T | 2 | a0001c0001t0006g0064a0001c0001t0042g0065 | 2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.27+23756G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232140 | ||||||
| chr5:80232170
|
C | T | 7 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0069others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+23726G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232170 | ||||||
| chr5:80232171
|
A | G | 7 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0069others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+23725T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232171 | ||||||
| chr5:80232172
|
A | C | 7 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0069others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+23724T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232172 | ||||||
| chr5:80232175
|
C | T | 7 | a0001c0001t0002g0277a0001c0001t0006g0064a0001c0001t0007g0069others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+23721G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232175 | ||||||
| chr5:80232187
|
G | A | 1 | a0001c0001t0024g0165 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.27+23709C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232187 | ||||||
| chr5:80232201
|
A | G | 1 | a0001c0001t0002g0027 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.27+23695T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232201 | ||||||
| chr5:80232207
|
A | G | 8 | a0001c0001t0001g0043a0001c0001t0004g0048a0001c0001t0004g0049others(5): Show | 8 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.27+23689T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232207 | ||||||
| chr5:80232213
|
G | A | 1 | a0001c0002t0003g0193 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.27+23683C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232213 | ||||||
| chr5:80232220
|
C | A | 1 | a0001c0002t0016g0034 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.27+23676G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232220 | ||||||
| chr5:80232221
|
C | G | 6 | a0001c0001t0001g0022a0001c0001t0002g0024a0001c0001t0002g0025others(3): Show | 6 | HG00099.hp2 HG01099.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+23675G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232221 | ||||||
| chr5:80232222
|
G | A | 1 | a0001c0001t0010g0235 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.27+23674C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232222 | ||||||
| chr5:80232224
|
A | G | 6 | a0001c0001t0001g0022a0001c0001t0002g0024a0001c0001t0002g0025others(3): Show | 6 | HG00099.hp2 HG01099.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+23672T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232224 | ||||||
| chr5:80232241
|
A | G | 1 | a0001c0002t0016g0034 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.27+23655T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232241 | ||||||
| chr5:80232246
|
T | C | 152 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(149): Show | 152 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.27+23650A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232246 | ||||||
| chr5:80232248
|
C | CA | 6 | a0001c0001t0001g0227a0001c0001t0002g0071a0001c0001t0015g0256others(3): Show | 6 | HG02083.hp2 HG02818.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.27+23647dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232248 | ||||||
| chr5:80232250
|
A | C | 24 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0002g0047others(21): Show | 24 | HG00642.hp1 HG00735.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.27+23646T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232250 | ||||||
| chr5:80232255
|
A | T | 1 | a0001c0002t0016g0034 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.27+23641T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232255 | ||||||
| chr5:80232256
|
A | T | 1 | a0001c0002t0016g0034 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.27+23640T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232256 | ||||||
| chr5:80232261
|
G | A | 1 | a0001c0002t0016g0034 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.27+23635C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232261 | ||||||
| chr5:80232265
|
G | A | 146 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0022others(143): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.27+23631C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232265 | ||||||
| chr5:80232273
|
A | G | 1 | a0001c0002t0016g0034 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.27+23623T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232273 | ||||||
| chr5:80232277
|
C | G | 1 | a0001c0002t0016g0034 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.27+23619G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232277 | ||||||
| chr5:80232403
|
CA | C | 108 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(105): Show | 108 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.27+23492delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232403 | ||||||
| chr5:80232406
|
A | G | 6 | a0001c0001t0004g0099a0001c0001t0018g0002a0001c0001t0018g0003others(3): Show | 6 | HG01168.hp2 HG01169.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.27+23490T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232406 | ||||||
| chr5:80232407
|
G | GA | 11 | a0001c0001t0001g0269a0001c0001t0002g0191a0001c0001t0002g0270others(8): Show | 11 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.27+23488dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232407 | ||||||
| chr5:80232408
|
A | G | 108 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(105): Show | 108 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.27+23488T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232408 | ||||||
| chr5:80232599
|
C | T | 89 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(86): Show | 89 | HG00099.hp2 HG01099.hp1 HG01109.hp2 others(86): Show |
intron_variant | MODIFIER | c.27+23297G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232599 | ||||||
| chr5:80232671
|
A | G | 86 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(83): Show | 86 | HG00099.hp2 HG01099.hp1 HG01109.hp2 others(83): Show |
intron_variant | MODIFIER | c.27+23225T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232671 | ||||||
| chr5:80232709
|
A | G | 130 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.27+23187T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232709 | ||||||
| chr5:80232740
|
C | T | 7 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(4): Show | 7 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+23156G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232740 | ||||||
| chr5:80232772
|
A | G | 280 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(277): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.27+23124T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232772 | ||||||
| chr5:80232789
|
A | T | 99 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.27+23107T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232789 | ||||||
| chr5:80232790
|
A | T | 1 | a0001c0002t0005g0137 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.27+23106T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232790 | ||||||
| chr5:80232791
|
A | T | 3 | a0001c0001t0020g0057a0001c0001t0059g0059a0001c0002t0005g0058 | 3 | HG01243.hp1 HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.27+23105T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232791 | ||||||
| chr5:80232818
|
C | T | 2 | a0001c0001t0007g0249a0001c0002t0067g0250 | 2 | HG00140.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.27+23078G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232818 | ||||||
| chr5:80232820
|
T | A | 1 | a0001c0001t0012g0180 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.27+23076A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232820 | ||||||
| chr5:80232915
|
A | G | 85 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(82): Show | 85 | HG00099.hp2 HG01099.hp1 HG01109.hp2 others(82): Show |
intron_variant | MODIFIER | c.27+22981T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232915 | ||||||
| chr5:80232964
|
G | A | 5 | a0001c0001t0009g0139a0001c0001t0021g0141a0001c0001t0033g0060others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+22932C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80232964 | ||||||
| chr5:80233003
|
T | C | 2 | a0001c0002t0005g0105a0001c0002t0005g0122 | 2 | NA18955.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.27+22893A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233003 | ||||||
| chr5:80233153
|
C | T | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+22743G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233153 | ||||||
| chr5:80233154
|
A | G | 126 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(123): Show | 126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.27+22742T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233154 | ||||||
| chr5:80233182
|
T | A | 96 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.27+22714A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233182 | ||||||
| chr5:80233216
|
G | A | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+22680C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233216 | ||||||
| chr5:80233289
|
T | C | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(6): Show | 9 | HG02135.hp1 NA18955.hp2 NA18957.hp2 others(6): Show |
intron_variant | MODIFIER | c.27+22607A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233289 | ||||||
| chr5:80233323
|
AG | A | 106 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(103): Show | 106 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.27+22572delC | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233323 | ||||||
| chr5:80233351
|
C | G | 1 | a0001c0002t0073g0204 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.27+22545G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233351 | ||||||
| chr5:80233351
|
C | T | 4 | a0001c0001t0009g0139a0001c0001t0021g0141a0001c0001t0033g0060others(1): Show | 4 | HG02280.hp1 HG03098.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+22545G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233351 | ||||||
| chr5:80233367
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.27+22529G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233367 | ||||||
| chr5:80233430
|
A | AATATTAT others(27): Show |
1 | a0001c0001t0075g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.27+22465_27+22466i others(36): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233430 | ||||||
| chr5:80233435
|
C | T | 1 | a0001c0001t0075g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.27+22461G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233435 | ||||||
| chr5:80233474
|
T | C | 54 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(51): Show | 54 | HG00099.hp2 HG01099.hp1 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.27+22422A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233474 | ||||||
| chr5:80233499
|
C | CAAAT | 99 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.27+22396_27+22397i others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233499 | ||||||
| chr5:80233527
|
A | T | 2 | a0001c0001t0009g0208a0001c0001t0048g0143 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.27+22369T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233527 | ||||||
| chr5:80233541
|
G | A | 1 | a0001c0002t0017g0072 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.27+22355C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233541 | ||||||
| chr5:80233577
|
T | C | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+22319A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233577 | ||||||
| chr5:80233687
|
A | G | 99 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.27+22209T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233687 | ||||||
| chr5:80233751
|
G | A | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.27+22145C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233751 | ||||||
| chr5:80233757
|
T | C | 4 | a0001c0001t0002g0277a0001c0001t0007g0069a0001c0001t0053g0061others(1): Show | 4 | HG01243.hp2 HG01884.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+22139A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233757 | ||||||
| chr5:80233773
|
C | T | 2 | a0001c0002t0005g0105a0001c0002t0005g0122 | 2 | NA18955.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.27+22123G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233773 | ||||||
| chr5:80233776
|
G | A | 128 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(125): Show | 128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.27+22120C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233776 | ||||||
| chr5:80233804
|
A | AC | 63 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(60): Show | 63 | HG00099.hp2 HG01099.hp1 HG01168.hp1 others(60): Show |
intron_variant | MODIFIER | c.27+22091dupG | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233804 | ||||||
| chr5:80233805
|
C | CCT | 16 | a0001c0001t0002g0215a0001c0001t0002g0277a0001c0001t0004g0221others(13): Show | 16 | HG01243.hp2 HG01516.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.27+22090_27+22091i others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233805 | ||||||
| chr5:80233805
|
C | CCTT | 5 | a0001c0001t0001g0151a0001c0001t0002g0163a0001c0001t0046g0260others(2): Show | 5 | HG01109.hp2 HG01515.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+22090_27+22091i others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233805 | ||||||
| chr5:80233805
|
C | CT | 34 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0200others(31): Show | 34 | HG00323.hp2 HG00741.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.27+22090dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233805 | ||||||
| chr5:80233805
|
C | CTT | 8 | a0001c0001t0002g0047a0001c0001t0002g0093a0001c0001t0004g0048others(5): Show | 8 | HG00642.hp1 HG01255.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.27+22089_27+22090d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233805 | ||||||
| chr5:80233805
|
CT | C | 12 | a0001c0001t0001g0103a0001c0001t0001g0271a0001c0001t0002g0018others(9): Show | 12 | HG00140.hp1 HG01070.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.27+22090delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233805 | ||||||
| chr5:80233805
|
CTTT | C | 7 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(4): Show | 7 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+22088_27+22090d others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233805 | ||||||
| chr5:80233805
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0003g0168 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.27+22081_27+22090d others(12): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233805 | ||||||
| chr5:80233806
|
T | C | 11 | a0001c0001t0001g0187a0001c0001t0002g0134a0001c0001t0004g0020others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.27+22090A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233806 | ||||||
| chr5:80233807
|
T | C | 3 | a0001c0001t0007g0249a0001c0001t0012g0131a0001c0001t0047g0261 | 3 | HG00140.hp1 HG01167.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.27+22089A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233807 | ||||||
| chr5:80233816
|
T | C | 1 | a0001c0002t0003g0168 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.27+22080A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233816 | ||||||
| chr5:80233835
|
A | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(32): Show | 35 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.27+22061T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233835 | ||||||
| chr5:80233870
|
G | A | 1 | a0001c0001t0013g0140 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.27+22026C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233870 | ||||||
| chr5:80233881
|
G | T | 96 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.27+22015C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233881 | ||||||
| chr5:80233954
|
G | A | 107 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(104): Show | 107 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.27+21942C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233954 | ||||||
| chr5:80233962
|
C | A | 99 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.27+21934G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233962 | ||||||
| chr5:80233973
|
A | G | 99 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.27+21923T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80233973 | ||||||
| chr5:80234090
|
G | A | 4 | a0001c0001t0002g0277a0001c0001t0007g0069a0001c0001t0053g0061others(1): Show | 4 | HG01243.hp2 HG01884.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+21806C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80234090 | ||||||
| chr5:80234100
|
A | G | 98 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(95): Show | 98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.27+21796T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80234100 | ||||||
| chr5:80234173
|
T | C | 98 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(95): Show | 98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.27+21723A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80234173 | ||||||
| chr5:80234307
|
C | T | 2 | a0001c0006t0020g0127a0001c0006t0045g0128 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.27+21589G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80234307 | ||||||
| chr5:80234462
|
T | C | 3 | a0001c0001t0007g0142a0002c0005t0019g0042a0002c0005t0019g0273 | 3 | HG01109.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.27+21434A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80234462 | ||||||
| chr5:80234487
|
C | T | 65 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(62): Show | 65 | HG00099.hp2 HG01099.hp1 HG01168.hp1 others(62): Show |
intron_variant | MODIFIER | c.27+21409G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80234487 | ||||||
| chr5:80234572
|
A | G | 3 | a0001c0001t0007g0069a0001c0001t0053g0061a0001c0002t0027g0148 | 3 | HG01884.hp2 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.27+21324T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80234572 | ||||||
| chr5:80234651
|
C | T | 2 | a0001c0001t0007g0069a0001c0001t0053g0061 | 2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.27+21245G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80234651 | ||||||
| chr5:80234752
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.27+21144C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80234752 | ||||||
| chr5:80234766
|
C | A | 1 | a0001c0002t0017g0145 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.27+21130G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80234766 | ||||||
| chr5:80234890
|
C | A | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+21006G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80234890 | ||||||
| chr5:80235045
|
C | G | 1 | a0001c0001t0004g0171 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.27+20851G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80235045 | ||||||
| chr5:80235057
|
T | A | 25 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0002g0047others(22): Show | 25 | HG00642.hp1 HG01074.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.27+20839A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80235057 | ||||||
| chr5:80235474
|
T | C | 4 | a0001c0001t0001g0151a0001c0001t0007g0150a0001c0001t0013g0068others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+20422A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80235474 | ||||||
| chr5:80235610
|
G | A | 2 | a0001c0001t0002g0211a0001c0001t0064g0212 | 2 | HG01168.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.27+20286C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80235610 | ||||||
| chr5:80235707
|
G | A | 2 | a0001c0001t0008g0241a0001c0001t0049g0242 | 2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.27+20189C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80235707 | ||||||
| chr5:80235785
|
G | A | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+20111C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80235785 | ||||||
| chr5:80235874
|
TTC | T | 14 | a0001c0001t0001g0133a0001c0001t0002g0134a0001c0001t0004g0020others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.27+20020_27+20021d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80235874 | ||||||
| chr5:80235896
|
T | G | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.27+20000A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80235896 | ||||||
| chr5:80235920
|
C | T | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+19976G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80235920 | ||||||
| chr5:80235976
|
A | T | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+19920T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80235976 | ||||||
| chr5:80236042
|
G | A | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+19854C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236042 | ||||||
| chr5:80236043
|
G | A | 5 | a0001c0001t0009g0139a0001c0001t0021g0141a0001c0001t0033g0060others(2): Show | 5 | HG02280.hp1 HG03098.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+19853C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236043 | ||||||
| chr5:80236049
|
T | C | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+19847A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236049 | ||||||
| chr5:80236180
|
T | A | 1 | a0001c0001t0014g0019 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.27+19716A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236180 | ||||||
| chr5:80236203
|
G | A | 4 | a0001c0001t0001g0151a0001c0001t0007g0150a0001c0001t0013g0068others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+19693C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236203 | ||||||
| chr5:80236226
|
G | A | 1 | a0001c0001t0013g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27+19670C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236226 | ||||||
| chr5:80236233
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.27+19663G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236233 | ||||||
| chr5:80236263
|
T | A | 1 | a0001c0001t0014g0019 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.27+19633A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236263 | ||||||
| chr5:80236311
|
A | G | 22 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0002g0047others(19): Show | 22 | HG00642.hp1 HG01074.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.27+19585T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236311 | ||||||
| chr5:80236418
|
A | T | 10 | a0001c0001t0001g0268a0001c0001t0002g0163a0001c0001t0008g0267others(7): Show | 10 | HG00639.hp2 HG01106.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.27+19478T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236418 | ||||||
| chr5:80236420
|
A | G | 2 | a0001c0001t0002g0211a0001c0001t0064g0212 | 2 | HG01168.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.27+19476T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236420 | ||||||
| chr5:80236425
|
C | T | 22 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0002g0047others(19): Show | 22 | HG00642.hp1 HG01074.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.27+19471G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236425 | ||||||
| chr5:80236527
|
CT | C | 10 | a0001c0001t0001g0088a0001c0001t0002g0071a0001c0001t0002g0211others(7): Show | 10 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.27+19368delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236527 | ||||||
| chr5:80236542
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.27+19354A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236542 | ||||||
| chr5:80236633
|
C | A | 6 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(3): Show | 6 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.27+19263G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236633 | ||||||
| chr5:80236674
|
C | T | 45 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0153others(42): Show | 45 | HG01168.hp1 HG01496.hp2 HG01516.hp1 others(42): Show |
intron_variant | MODIFIER | c.27+19222G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236674 | ||||||
| chr5:80236780
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.27+19116C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236780 | ||||||
| chr5:80236937
|
T | C | 129 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(126): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.27+18959A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236937 | ||||||
| chr5:80236972
|
C | T | 3 | a0001c0001t0014g0019a0001c0002t0005g0105a0001c0002t0005g0122 | 3 | NA18955.hp1 NA18955.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.27+18924G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236972 | ||||||
| chr5:80236976
|
C | T | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.27+18920G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80236976 | ||||||
| chr5:80237078
|
C | T | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.27+18818G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237078 | ||||||
| chr5:80237090
|
G | A | 7 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(4): Show | 7 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+18806C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237090 | ||||||
| chr5:80237119
|
G | A | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.27+18777C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237119 | ||||||
| chr5:80237199
|
G | C | 98 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(95): Show | 98 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.27+18697C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237199 | ||||||
| chr5:80237345
|
C | CT | 94 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.27+18550dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237345 | ||||||
| chr5:80237345
|
C | CTT | 22 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0002g0047others(19): Show | 22 | HG00642.hp1 HG01074.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.27+18549_27+18550d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237345 | ||||||
| chr5:80237414
|
G | C | 11 | a0001c0001t0001g0269a0001c0001t0002g0270a0001c0001t0008g0259others(8): Show | 11 | HG02572.hp2 HG02818.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.27+18482C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237414 | ||||||
| chr5:80237461
|
G | A | 1 | a0001c0001t0009g0226 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.27+18435C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237461 | ||||||
| chr5:80237546
|
G | A | 1 | a0001c0001t0013g0140 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.27+18350C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237546 | ||||||
| chr5:80237564
|
G | A | 1 | a0001c0002t0003g0224 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.27+18332C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237564 | ||||||
| chr5:80237775
|
A | G | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+18121T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237775 | ||||||
| chr5:80237811
|
A | T | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+18085T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237811 | ||||||
| chr5:80237831
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.27+18065G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237831 | ||||||
| chr5:80237856
|
C | A | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.27+18040G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237856 | ||||||
| chr5:80237898
|
A | G | 2 | a0001c0001t0002g0280a0001c0001t0007g0281 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.27+17998T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237898 | ||||||
| chr5:80237905
|
C | G | 2 | a0001c0001t0012g0131a0001c0002t0005g0054 | 2 | HG02148.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.27+17991G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237905 | ||||||
| chr5:80237965
|
G | A | 2 | a0001c0001t0001g0029a0001c0002t0016g0033 | 2 | NA18948.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.27+17931C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237965 | ||||||
| chr5:80237974
|
C | T | 1 | a0001c0001t0013g0140 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.27+17922G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80237974 | ||||||
| chr5:80238059
|
G | A | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+17837C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238059 | ||||||
| chr5:80238103
|
C | CA | 75 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(72): Show | 75 | HG00099.hp2 HG01069.hp2 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.27+17792dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238103 | ||||||
| chr5:80238103
|
C | CAA | 14 | a0001c0001t0001g0133a0001c0001t0002g0134a0001c0001t0004g0021others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.27+17791_27+17792d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238103 | ||||||
| chr5:80238103
|
CA | C | 8 | a0001c0001t0001g0007a0001c0001t0004g0084a0001c0001t0009g0139others(5): Show | 8 | HG02280.hp1 HG02451.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.27+17792delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238103 | ||||||
| chr5:80238151
|
G | A | 15 | a0001c0001t0001g0133a0001c0001t0002g0134a0001c0001t0004g0020others(12): Show | 15 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.27+17745C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238151 | ||||||
| chr5:80238313
|
G | A | 1 | a0001c0002t0003g0026 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.27+17583C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238313 | ||||||
| chr5:80238342
|
C | G | 127 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(124): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.27+17554G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238342 | ||||||
| chr5:80238356
|
T | C | 14 | a0001c0001t0001g0133a0001c0001t0002g0134a0001c0001t0004g0020others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.27+17540A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238356 | ||||||
| chr5:80238405
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.27+17491A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238405 | ||||||
| chr5:80238427
|
G | A | 7 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(4): Show | 7 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+17469C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238427 | ||||||
| chr5:80238460
|
C | G | 7 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(4): Show | 7 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+17436G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238460 | ||||||
| chr5:80238620
|
C | T | 3 | a0001c0001t0007g0142a0002c0005t0019g0042a0002c0005t0019g0273 | 3 | HG01109.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.27+17276G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238620 | ||||||
| chr5:80238644
|
G | A | 3 | a0001c0001t0007g0142a0002c0005t0019g0042a0002c0005t0019g0273 | 3 | HG01109.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.27+17252C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238644 | ||||||
| chr5:80238665
|
C | A | 1 | a0001c0001t0013g0140 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.27+17231G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238665 | ||||||
| chr5:80238769
|
A | C | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+17127T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238769 | ||||||
| chr5:80238788
|
C | CA | 12 | a0001c0001t0001g0225a0001c0001t0002g0109a0001c0001t0004g0138others(9): Show | 12 | HG01175.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.27+17107dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238788 | ||||||
| chr5:80238788
|
CA | C | 24 | a0001c0001t0001g0103a0001c0001t0001g0133a0001c0001t0001g0151others(21): Show | 24 | HG00408.hp2 HG01099.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.27+17107delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238788 | ||||||
| chr5:80238788
|
CAA | C | 91 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0043others(88): Show | 91 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.27+17106_27+17107d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238788 | ||||||
| chr5:80238788
|
CAAA | C | 12 | a0001c0001t0001g0269a0001c0001t0002g0270a0001c0001t0008g0259others(9): Show | 12 | HG02572.hp2 HG02818.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.27+17105_27+17107d others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238788 | ||||||
| chr5:80238851
|
A | C | 1 | a0001c0001t0002g0044 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.27+17045T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238851 | ||||||
| chr5:80238944
|
G | C | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+16952C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80238944 | ||||||
| chr5:80239031
|
C | T | 122 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0043others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.27+16865G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239031 | ||||||
| chr5:80239035
|
C | T | 51 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0153others(48): Show | 51 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(48): Show |
intron_variant | MODIFIER | c.27+16861G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239035 | ||||||
| chr5:80239041
|
G | A | 1 | a0001c0001t0013g0140 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.27+16855C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239041 | ||||||
| chr5:80239075
|
T | C | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+16821A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239075 | ||||||
| chr5:80239146
|
G | A | 4 | a0001c0001t0001g0151a0001c0001t0007g0150a0001c0001t0013g0068others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+16750C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239146 | ||||||
| chr5:80239159
|
C | G | 11 | a0001c0001t0001g0269a0001c0001t0002g0270a0001c0001t0008g0259others(8): Show | 11 | HG02572.hp2 HG02818.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.27+16737G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239159 | ||||||
| chr5:80239213
|
G | A | 5 | a0001c0001t0002g0163a0001c0001t0007g0142a0001c0001t0063g0164others(2): Show | 5 | HG01109.hp1 HG01109.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+16683C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239213 | ||||||
| chr5:80239242
|
C | A | 10 | a0001c0001t0001g0268a0001c0001t0002g0163a0001c0001t0008g0267others(7): Show | 10 | HG00639.hp2 HG01106.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.27+16654G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239242 | ||||||
| chr5:80239282
|
A | C | 101 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.27+16614T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239282 | ||||||
| chr5:80239414
|
C | CT | 285 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.27+16481dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239414 | ||||||
| chr5:80239432
|
A | G | 19 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0002g0047others(16): Show | 19 | HG00642.hp1 HG01074.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.27+16464T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239432 | ||||||
| chr5:80239467
|
C | CT | 7 | a0001c0001t0001g0006a0001c0001t0004g0199a0001c0001t0006g0178others(4): Show | 7 | HG01109.hp1 HG01175.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+16428dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239467 | ||||||
| chr5:80239467
|
CT | C | 110 | a0001c0001t0001g0014a0001c0001t0001g0022a0001c0001t0001g0029others(107): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.27+16428delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239467 | ||||||
| chr5:80239467
|
CTT | C | 15 | a0001c0001t0001g0151a0001c0001t0002g0211a0001c0001t0007g0150others(12): Show | 15 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.27+16427_27+16428d others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239467 | ||||||
| chr5:80239615
|
G | A | 62 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0153others(59): Show | 62 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(59): Show |
intron_variant | MODIFIER | c.27+16281C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239615 | ||||||
| chr5:80239679
|
C | T | 1 | a0001c0001t0032g0004 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.27+16217G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239679 | ||||||
| chr5:80239700
|
A | G | 1 | a0001c0002t0003g0031 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.27+16196T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239700 | ||||||
| chr5:80239847
|
T | C | 3 | a0001c0001t0007g0142a0002c0005t0019g0042a0002c0005t0019g0273 | 3 | HG01109.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.27+16049A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239847 | ||||||
| chr5:80239880
|
G | C | 3 | a0001c0001t0007g0142a0002c0005t0019g0042a0002c0005t0019g0273 | 3 | HG01109.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.27+16016C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80239880 | ||||||
| chr5:80240192
|
A | C | 1 | a0001c0002t0067g0250 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.27+15704T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80240192 | ||||||
| chr5:80240249
|
T | A | 15 | a0001c0001t0001g0133a0001c0001t0002g0134a0001c0001t0004g0020others(12): Show | 15 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.27+15647A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80240249 | ||||||
| chr5:80240365
|
T | C | 1 | a0001c0002t0003g0108 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.27+15531A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80240365 | ||||||
| chr5:80240899
|
C | T | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+14997G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80240899 | ||||||
| chr5:80241197
|
A | G | 3 | a0001c0001t0008g0129a0001c0006t0020g0127a0001c0006t0045g0128 | 3 | HG02451.hp2 HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.27+14699T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80241197 | ||||||
| chr5:80241226
|
T | C | 66 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(63): Show | 66 | HG00099.hp2 HG01099.hp1 HG01168.hp1 others(63): Show |
intron_variant | MODIFIER | c.27+14670A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80241226 | ||||||
| chr5:80241252
|
CGAGGTCA others(1): Show |
C | 66 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(63): Show | 66 | HG00099.hp2 HG01099.hp1 HG01168.hp1 others(63): Show |
intron_variant | MODIFIER | c.27+14636_27+14643d others(10): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80241252 | ||||||
| chr5:80241253
|
G | A | 4 | a0001c0001t0001g0151a0001c0001t0007g0150a0001c0001t0013g0068others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+14643C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80241253 | ||||||
| chr5:80241281
|
C | T | 4 | a0001c0002t0003g0078a0001c0002t0003g0079a0001c0002t0003g0080others(1): Show | 4 | HG01255.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+14615G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80241281 | ||||||
| chr5:80241373
|
G | A | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+14523C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80241373 | ||||||
| chr5:80241426
|
G | A | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.27+14470C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80241426 | ||||||
| chr5:80241444
|
G | A | 4 | a0001c0001t0001g0151a0001c0001t0007g0150a0001c0001t0013g0068others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+14452C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80241444 | ||||||
| chr5:80241480
|
G | T | 14 | a0001c0001t0001g0089a0001c0001t0002g0163a0001c0001t0008g0259others(11): Show | 14 | HG01109.hp2 HG01167.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.27+14416C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80241480 | ||||||
| chr5:80241692
|
A | C | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+14204T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80241692 | ||||||
| chr5:80241698
|
C | T | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+14198G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80241698 | ||||||
| chr5:80241735
|
G | A | 24 | a0001c0001t0001g0133a0001c0001t0001g0268a0001c0001t0002g0134others(21): Show | 24 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.27+14161C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80241735 | ||||||
| chr5:80241809
|
T | C | 1 | a0001c0001t0004g0048 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.27+14087A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80241809 | ||||||
| chr5:80241810
|
G | A | 3 | a0001c0001t0008g0129a0001c0006t0020g0127a0001c0006t0045g0128 | 3 | HG02451.hp2 HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.27+14086C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80241810 | ||||||
| chr5:80241909
|
A | G | 1 | a0001c0002t0005g0214 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.27+13987T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80241909 | ||||||
| chr5:80241916
|
G | A | 1 | a0001c0002t0005g0214 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.27+13980C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80241916 | ||||||
| chr5:80242222
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.27+13674C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80242222 | ||||||
| chr5:80242240
|
T | G | 1 | a0001c0001t0004g0073 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.27+13656A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80242240 | ||||||
| chr5:80242401
|
T | C | 61 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0153others(58): Show | 61 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(58): Show |
intron_variant | MODIFIER | c.27+13495A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80242401 | ||||||
| chr5:80242507
|
A | AT | 285 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.27+13388dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80242507 | ||||||
| chr5:80242516
|
G | GC | 285 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.27+13379dupG | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80242516 | ||||||
| chr5:80242522
|
C | T | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.27+13374G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80242522 | ||||||
| chr5:80242613
|
A | G | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+13283T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80242613 | ||||||
| chr5:80242640
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.27+13256G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80242640 | ||||||
| chr5:80242682
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0010g0183 | 2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.27+13214C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80242682 | ||||||
| chr5:80242780
|
G | A | 23 | a0001c0001t0001g0133a0001c0001t0001g0268a0001c0001t0002g0134others(20): Show | 23 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.27+13116C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80242780 | ||||||
| chr5:80242881
|
C | A | 1 | a0001c0001t0002g0097 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.27+13015G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80242881 | ||||||
| chr5:80243015
|
C | A | 3 | a0001c0001t0008g0129a0001c0006t0020g0127a0001c0006t0045g0128 | 3 | HG02451.hp2 HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.27+12881G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243015 | ||||||
| chr5:80243031
|
C | T | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+12865G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243031 | ||||||
| chr5:80243043
|
T | G | 7 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(4): Show | 7 | HG00639.hp2 HG01106.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+12853A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243043 | ||||||
| chr5:80243109
|
G | C | 128 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0043others(125): Show | 128 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(125): Show |
intron_variant | MODIFIER | c.27+12787C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243109 | ||||||
| chr5:80243134
|
T | C | 1 | a0001c0001t0029g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.27+12762A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243134 | ||||||
| chr5:80243318
|
C | A | 1 | a0002c0003t0009g0228 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.27+12578G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243318 | ||||||
| chr5:80243362
|
A | G | 4 | a0001c0001t0001g0153a0001c0001t0001g0187a0001c0002t0003g0186others(1): Show | 4 | HG01496.hp2 HG01975.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+12534T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243362 | ||||||
| chr5:80243470
|
A | T | 2 | a0001c0001t0002g0109a0001c0001t0029g0102 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.27+12426T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243470 | ||||||
| chr5:80243671
|
C | T | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+12225G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243671 | ||||||
| chr5:80243684
|
T | C | 1 | a0001c0001t0008g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.27+12212A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243684 | ||||||
| chr5:80243743
|
T | TTAAA | 104 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(101): Show | 104 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.27+12149_27+12152d others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243743 | ||||||
| chr5:80243743
|
T | TTAAATAA others(1): Show |
41 | a0001c0001t0001g0011a0001c0001t0001g0166a0001c0001t0001g0177others(38): Show | 41 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.27+12145_27+12152d others(10): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243743 | ||||||
| chr5:80243743
|
T | TTAAATAA others(5): Show |
2 | a0001c0001t0006g0178a0001c0001t0048g0143 | 2 | HG01175.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.27+12141_27+12152d others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243743 | ||||||
| chr5:80243743
|
TTAAA | T | 7 | a0001c0001t0002g0169a0001c0001t0006g0167a0001c0001t0007g0142others(4): Show | 7 | HG01109.hp1 HG01255.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+12149_27+12152d others(6): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243743 | ||||||
| chr5:80243743
|
TTAAATAA others(1): Show |
T | 5 | a0001c0001t0002g0025a0001c0001t0002g0094a0001c0001t0011g0123others(2): Show | 5 | HG01978.hp2 HG01993.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+12145_27+12152d others(10): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243743 | ||||||
| chr5:80243743
|
TTAAATAA others(5): Show |
T | 3 | a0001c0001t0002g0230a0001c0001t0008g0182a0001c0002t0003g0205 | 3 | HG02027.hp1 HG02027.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.27+12141_27+12152d others(14): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243743 | ||||||
| chr5:80243784
|
T | A | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.27+12112A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243784 | ||||||
| chr5:80243875
|
T | TTGA | 13 | a0001c0001t0001g0269a0001c0001t0002g0094a0001c0001t0002g0270others(10): Show | 13 | HG01891.hp1 HG01978.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.27+12018_27+12020d others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80243875 | ||||||
| chr5:80244057
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.27+11839G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80244057 | ||||||
| chr5:80244219
|
C | CT | 7 | a0001c0001t0007g0142a0001c0001t0010g0062a0001c0001t0047g0261others(4): Show | 7 | HG01109.hp1 HG01167.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+11676dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80244219 | ||||||
| chr5:80244255
|
A | G | 1 | a0001c0001t0050g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.27+11641T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80244255 | ||||||
| chr5:80244284
|
C | T | 1 | a0001c0001t0029g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.27+11612G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80244284 | ||||||
| chr5:80244294
|
C | CA | 7 | a0001c0001t0008g0259a0001c0001t0015g0256a0001c0001t0015g0258others(4): Show | 7 | HG02572.hp2 HG02818.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+11601dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80244294 | ||||||
| chr5:80244418
|
G | A | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+11478C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80244418 | ||||||
| chr5:80244458
|
C | T | 4 | a0001c0001t0002g0094a0001c0001t0011g0123a0001c0002t0003g0096others(1): Show | 4 | HG01978.hp2 HG02004.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+11438G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80244458 | ||||||
| chr5:80244619
|
G | A | 1 | a0001c0002t0003g0036 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.27+11277C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80244619 | ||||||
| chr5:80244640
|
A | G | 129 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(126): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.27+11256T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80244640 | ||||||
| chr5:80244694
|
C | T | 1 | a0001c0001t0008g0241 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.27+11202G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80244694 | ||||||
| chr5:80244738
|
C | T | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.27+11158G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80244738 | ||||||
| chr5:80244957
|
A | G | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+10939T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80244957 | ||||||
| chr5:80244990
|
C | T | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+10906G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80244990 | ||||||
| chr5:80245023
|
G | C | 1 | a0001c0002t0073g0204 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.27+10873C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245023 | ||||||
| chr5:80245171
|
C | T | 1 | a0001c0001t0002g0025 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.27+10725G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245171 | ||||||
| chr5:80245188
|
G | GT | 4 | a0001c0001t0002g0094a0001c0001t0011g0123a0001c0002t0003g0096others(1): Show | 4 | HG01978.hp2 HG02004.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+10707dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245188 | ||||||
| chr5:80245342
|
C | T | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.27+10554G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245342 | ||||||
| chr5:80245436
|
T | C | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.27+10460A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245436 | ||||||
| chr5:80245600
|
T | A | 1 | a0001c0001t0002g0219 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.27+10296A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245600 | ||||||
| chr5:80245605
|
A | AT | 14 | a0001c0001t0001g0133a0001c0001t0002g0134a0001c0001t0004g0020others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.27+10290dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245605 | ||||||
| chr5:80245609
|
A | AT | 108 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0030others(105): Show | 108 | HG00099.hp2 HG00642.hp1 HG01074.hp2 others(105): Show |
intron_variant | MODIFIER | c.27+10286dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245609 | ||||||
| chr5:80245609
|
A | T | 15 | a0001c0001t0001g0133a0001c0001t0002g0134a0001c0001t0004g0020others(12): Show | 15 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.27+10287T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245609 | ||||||
| chr5:80245612
|
T | TA | 4 | a0001c0001t0002g0094a0001c0001t0011g0123a0001c0002t0003g0096others(1): Show | 4 | HG01978.hp2 HG02004.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+10283_27+10284i others(3): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245612 | ||||||
| chr5:80245725
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.27+10171C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245725 | ||||||
| chr5:80245871
|
C | T | 1 | a0001c0002t0073g0204 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.27+10025G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245871 | ||||||
| chr5:80245911
|
G | A | 1 | a0001c0001t0029g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.27+9985C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245911 | ||||||
| chr5:80245965
|
T | TA | 6 | a0001c0001t0002g0094a0001c0001t0002g0109a0001c0001t0010g0235others(3): Show | 6 | HG01884.hp1 HG01978.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+9930dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245965 | ||||||
| chr5:80245965
|
TA | T | 147 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.27+9930delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245965 | ||||||
| chr5:80245965
|
TAA | T | 27 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0190others(24): Show | 27 | HG00323.hp1 HG01069.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.27+9929_27+9930del others(2): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245965 | ||||||
| chr5:80245965
|
TAAA | T | 54 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0133others(51): Show | 54 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.27+9928_27+9930del others(3): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245965 | ||||||
| chr5:80245967
|
A | T | 1 | a0001c0002t0003g0184 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.27+9929T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80245967 | ||||||
| chr5:80246001
|
CAAAAT | C | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG01496.hp1 HG02258.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+9890_27+9894del others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80246001 | ||||||
| chr5:80246263
|
G | C | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG01496.hp1 HG02258.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+9633C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80246263 | ||||||
| chr5:80246376
|
T | A | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG01496.hp1 HG02258.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+9520A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80246376 | ||||||
| chr5:80246410
|
C | T | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.27+9486G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80246410 | ||||||
| chr5:80246991
|
C | A | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+8905G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80246991 | ||||||
| chr5:80247301
|
T | C | 1 | a0002c0004t0005g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.27+8595A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80247301 | ||||||
| chr5:80247305
|
G | A | 17 | a0001c0001t0001g0133a0001c0001t0002g0134a0001c0001t0002g0163others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.27+8591C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80247305 | ||||||
| chr5:80247335
|
A | G | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.27+8561T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80247335 | ||||||
| chr5:80247369
|
C | T | 29 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0002g0047others(26): Show | 29 | HG00642.hp1 HG01074.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.27+8527G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80247369 | ||||||
| chr5:80247480
|
G | A | 19 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0002g0047others(16): Show | 19 | HG00642.hp1 HG01074.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.27+8416C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80247480 | ||||||
| chr5:80247534
|
T | C | 1 | a0001c0001t0002g0120 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.27+8362A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80247534 | ||||||
| chr5:80247550
|
C | T | 2 | a0001c0001t0002g0211a0001c0001t0064g0212 | 2 | HG01168.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.27+8346G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80247550 | ||||||
| chr5:80247563
|
T | G | 1 | a0001c0001t0002g0239 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.27+8333A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80247563 | ||||||
| chr5:80247818
|
C | T | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.27+8078G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80247818 | ||||||
| chr5:80248006
|
C | G | 2 | a0001c0001t0009g0208a0001c0009t0035g0209 | 2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.27+7890G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80248006 | ||||||
| chr5:80248015
|
G | T | 3 | a0001c0001t0008g0129a0001c0006t0020g0127a0001c0006t0045g0128 | 3 | HG02451.hp2 HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.27+7881C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80248015 | ||||||
| chr5:80248065
|
T | C | 1 | a0001c0001t0038g0111 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.27+7831A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80248065 | ||||||
| chr5:80248233
|
C | T | 2 | a0001c0001t0002g0163a0001c0001t0063g0164 | 2 | HG01109.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.27+7663G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80248233 | ||||||
| chr5:80248259
|
G | A | 6 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(3): Show | 6 | HG01496.hp1 HG02258.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+7637C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80248259 | ||||||
| chr5:80248288
|
G | T | 15 | a0001c0001t0001g0133a0001c0001t0002g0134a0001c0001t0004g0020others(12): Show | 15 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.27+7608C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80248288 | ||||||
| chr5:80248679
|
A | T | 10 | a0001c0001t0001g0269a0001c0001t0002g0094a0001c0001t0002g0270others(7): Show | 10 | HG01978.hp2 HG02004.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.27+7217T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80248679 | ||||||
| chr5:80248698
|
T | C | 1 | a0001c0002t0022g0272 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.27+7198A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80248698 | ||||||
| chr5:80248769
|
C | G | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.27+7127G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80248769 | ||||||
| chr5:80249087
|
G | T | 1 | a0001c0001t0001g0170 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.27+6809C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80249087 | ||||||
| chr5:80249142
|
G | A | 6 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(3): Show | 6 | HG01496.hp1 HG02258.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+6754C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80249142 | ||||||
| chr5:80249172
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.27+6724C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80249172 | ||||||
| chr5:80249208
|
G | A | 3 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0023g0220 | 3 | HG01167.hp1 HG01169.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.27+6688C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80249208 | ||||||
| chr5:80249302
|
G | A | 6 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(3): Show | 6 | HG01496.hp1 HG02258.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+6594C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80249302 | ||||||
| chr5:80249451
|
C | T | 4 | a0001c0001t0009g0226a0001c0001t0023g0220a0001c0002t0068g0188others(1): Show | 4 | HG03688.hp1 HG04184.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+6445G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80249451 | ||||||
| chr5:80249530
|
C | T | 1 | a0001c0002t0022g0272 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.27+6366G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80249530 | ||||||
| chr5:80249623
|
G | T | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+6273C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80249623 | ||||||
| chr5:80249759
|
G | A | 8 | a0001c0001t0008g0259a0001c0001t0015g0256a0001c0001t0015g0258others(5): Show | 8 | HG01167.hp2 HG02572.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.27+6137C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80249759 | ||||||
| chr5:80249797
|
C | G | 12 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0100others(9): Show | 12 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.27+6099G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80249797 | ||||||
| chr5:80249997
|
T | C | 5 | a0001c0001t0008g0259a0001c0001t0015g0256a0001c0001t0015g0258others(2): Show | 5 | HG02818.hp1 HG03225.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+5899A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80249997 | ||||||
| chr5:80250208
|
G | A | 4 | a0001c0001t0008g0129a0001c0002t0027g0148a0001c0006t0020g0127others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+5688C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80250208 | ||||||
| chr5:80250243
|
G | GA | 4 | a0001c0001t0002g0094a0001c0001t0011g0123a0001c0002t0003g0096others(1): Show | 4 | HG01978.hp2 HG02004.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+5652dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80250243 | ||||||
| chr5:80250343
|
C | T | 110 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0043others(107): Show | 110 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.27+5553G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80250343 | ||||||
| chr5:80250353
|
A | G | 8 | a0001c0001t0008g0259a0001c0001t0015g0256a0001c0001t0015g0258others(5): Show | 8 | HG01167.hp2 HG02572.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.27+5543T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80250353 | ||||||
| chr5:80250562
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.27+5334C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80250562 | ||||||
| chr5:80250587
|
A | C | 2 | a0001c0001t0022g0185a0001c0002t0003g0184 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.27+5309T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80250587 | ||||||
| chr5:80250596
|
G | C | 7 | a0001c0001t0001g0271a0001c0001t0002g0277a0001c0001t0007g0275others(4): Show | 7 | HG01243.hp2 HG02258.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.27+5300C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80250596 | ||||||
| chr5:80250622
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.27+5274C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80250622 | ||||||
| chr5:80250899
|
G | T | 1 | a0001c0001t0023g0130 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.27+4997C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80250899 | ||||||
| chr5:80250943
|
C | T | 1 | a0001c0001t0024g0165 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.27+4953G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80250943 | ||||||
| chr5:80250966
|
G | GT | 206 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.27+4929dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80250966 | ||||||
| chr5:80251054
|
A | G | 1 | a0001c0002t0072g0210 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.27+4842T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251054 | ||||||
| chr5:80251083
|
G | C | 2 | a0001c0001t0009g0208a0001c0009t0035g0209 | 2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.27+4813C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251083 | ||||||
| chr5:80251279
|
AATACATA others(5): Show |
A | 35 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0001g0232others(32): Show | 35 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.27+4605_27+4616del others(12): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251279 | ||||||
| chr5:80251279
|
AATACATA others(13): Show |
A | 4 | a0001c0001t0001g0151a0001c0001t0007g0150a0001c0001t0013g0068others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+4597_27+4616del others(20): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251279 | ||||||
| chr5:80251279
|
AATACATA others(17): Show |
A | 3 | a0001c0001t0008g0241a0001c0001t0049g0242a0001c0001t0058g0243 | 3 | HG01891.hp1 HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.27+4593_27+4616del others(24): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251279 | ||||||
| chr5:80251279
|
AATACATA others(21): Show |
A | 1 | a0001c0001t0041g0279 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27+4589_27+4616del others(28): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251279 | ||||||
| chr5:80251279
|
AATACATA others(25): Show |
A | 18 | a0001c0001t0001g0271a0001c0001t0002g0277a0001c0001t0002g0280others(15): Show | 18 | HG01167.hp2 HG01243.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.27+4585_27+4616del others(32): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251279 | ||||||
| chr5:80251282
|
ACATACAT others(1): Show |
A | 52 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0107others(49): Show | 52 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.27+4606_27+4613del others(8): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251282 | ||||||
| chr5:80251286
|
ACATG | A | 27 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0088others(24): Show | 27 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.27+4606_27+4609del others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251286 | ||||||
| chr5:80251290
|
G | A | 2 | a0001c0001t0002g0056a0001c0001t0051g0236 | 2 | HG02071.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.27+4606C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251290 | ||||||
| chr5:80251290
|
G | GCATA | 12 | a0001c0001t0001g0227a0001c0001t0002g0237a0001c0001t0002g0248others(9): Show | 12 | HG00733.hp1 HG01255.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.27+4602_27+4605dup others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251290 | ||||||
| chr5:80251290
|
GCATA | G | 36 | a0001c0001t0001g0022a0001c0001t0001g0153a0001c0001t0001g0187others(33): Show | 36 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.27+4602_27+4605del others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251290 | ||||||
| chr5:80251290
|
GCATACAT others(1): Show |
G | 47 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0039others(44): Show | 47 | HG00140.hp2 HG00621.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.27+4598_27+4605del others(8): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251290 | ||||||
| chr5:80251290
|
GCATACAT others(5): Show |
G | 1 | a0001c0001t0007g0249 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.27+4594_27+4605del others(12): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251290 | ||||||
| chr5:80251291
|
C | T | 1 | a0001c0001t0051g0236 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.27+4605G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251291 | ||||||
| chr5:80251295
|
C | T | 1 | a0001c0001t0010g0235 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.27+4601G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251295 | ||||||
| chr5:80251298
|
A | ACATG | 12 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(9): Show | 12 | HG00408.hp1 HG01943.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.27+4597_27+4598ins others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251298 | ||||||
| chr5:80251302
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.27+4594T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251302 | ||||||
| chr5:80251625
|
G | C | 1 | a0001c0001t0001g0028 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.27+4271C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251625 | ||||||
| chr5:80251729
|
C | CA | 40 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(37): Show | 40 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.27+4166dupT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251729 | ||||||
| chr5:80251729
|
C | CAA | 6 | a0001c0001t0008g0259a0001c0001t0015g0256a0001c0001t0015g0258others(3): Show | 6 | HG02818.hp1 HG03225.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.27+4165_27+4166dup others(2): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251729 | ||||||
| chr5:80251729
|
CA | C | 7 | a0001c0001t0001g0162a0001c0001t0001g0269a0001c0001t0002g0163others(4): Show | 7 | HG01109.hp2 HG01515.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+4166delT | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251729 | ||||||
| chr5:80251738
|
A | T | 1 | a0001c0001t0002g0237 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.27+4158T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251738 | ||||||
| chr5:80251780
|
C | T | 117 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0039others(114): Show | 117 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.27+4116G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251780 | ||||||
| chr5:80251781
|
A | G | 180 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(177): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.27+4115T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251781 | ||||||
| chr5:80251860
|
C | T | 1 | a0001c0001t0002g0278 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.27+4036G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251860 | ||||||
| chr5:80251897
|
T | TATCAGAG others(485): Show |
1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.27+3998_27+3999ins others(492): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251897 | ||||||
| chr5:80251897
|
T | TATCAGAG others(486): Show |
108 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0039others(105): Show | 108 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.27+3998_27+3999ins others(493): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251897 | ||||||
| chr5:80251897
|
T | TATCAGAG others(486): Show |
9 | a0001c0001t0001g0151a0001c0001t0007g0150a0001c0001t0007g0249others(6): Show | 9 | HG00140.hp1 HG00642.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.27+3998_27+3999ins others(493): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251897 | ||||||
| chr5:80251897
|
T | TATCAGAG others(486): Show |
34 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(31): Show | 34 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.27+3998_27+3999ins others(493): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251897 | ||||||
| chr5:80251897
|
T | TATCAGAG others(486): Show |
1 | a0001c0001t0008g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.27+3998_27+3999ins others(493): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251897 | ||||||
| chr5:80251897
|
T | TATCAGAG others(486): Show |
1 | a0001c0001t0075g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.27+3998_27+3999ins others(493): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251897 | ||||||
| chr5:80251900
|
T | A | 154 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(151): Show | 154 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.27+3996A>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251900 | ||||||
| chr5:80251922
|
A | T | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.27+3974T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80251922 | ||||||
| chr5:80252058
|
C | CT | 6 | a0001c0001t0001g0271a0001c0001t0002g0056a0001c0001t0020g0057others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+3837dupA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80252058 | ||||||
| chr5:80252058
|
CT | C | 54 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(51): Show | 54 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.27+3837delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80252058 | ||||||
| chr5:80252058
|
CTT | C | 15 | a0001c0001t0001g0133a0001c0001t0002g0134a0001c0001t0002g0136others(12): Show | 15 | HG00140.hp2 HG00735.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.27+3836_27+3837del others(2): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80252058 | ||||||
| chr5:80252058
|
CTTT | C | 10 | a0001c0001t0002g0157a0001c0001t0004g0247a0001c0001t0007g0158others(7): Show | 10 | HG00609.hp2 HG01891.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.27+3835_27+3837del others(3): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80252058 | ||||||
| chr5:80252058
|
CTTTT | C | 105 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0039others(102): Show | 105 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.27+3834_27+3837del others(4): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80252058 | ||||||
| chr5:80252161
|
A | C | 1 | a0001c0002t0005g0054 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.27+3735T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80252161 | ||||||
| chr5:80252248
|
C | G | 1 | a0001c0001t0021g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.27+3648G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80252248 | ||||||
| chr5:80252248
|
C | T | 9 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(6): Show | 9 | HG01346.hp1 HG01433.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.27+3648G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80252248 | ||||||
| chr5:80252312
|
G | A | 2 | a0001c0001t0002g0237a0001c0001t0012g0238 | 2 | HG00733.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.27+3584C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80252312 | ||||||
| chr5:80252455
|
C | T | 109 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0039others(106): Show | 109 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.27+3441G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80252455 | ||||||
| chr5:80252541
|
A | G | 3 | a0001c0001t0007g0249a0001c0001t0012g0251a0001c0002t0067g0250 | 3 | HG00140.hp1 HG00642.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.27+3355T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80252541 | ||||||
| chr5:80252603
|
C | T | 1 | a0001c0001t0014g0152 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.27+3293G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80252603 | ||||||
| chr5:80252660
|
G | T | 117 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0039others(114): Show | 117 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.27+3236C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80252660 | ||||||
| chr5:80252697
|
T | C | 3 | a0001c0001t0001g0151a0001c0001t0007g0150a0001c0001t0044g0149 | 3 | HG02486.hp1 HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.27+3199A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80252697 | ||||||
| chr5:80252753
|
G | C | 1 | a0001c0001t0002g0278 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.27+3143C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80252753 | ||||||
| chr5:80252907
|
G | C | 1 | a0001c0001t0002g0278 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.27+2989C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80252907 | ||||||
| chr5:80252928
|
G | A | 1 | a0001c0001t0047g0261 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.27+2968C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80252928 | ||||||
| chr5:80253010
|
C | G | 4 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(1): Show | 4 | HG01496.hp1 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+2886G>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253010 | ||||||
| chr5:80253023
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.27+2873G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253023 | ||||||
| chr5:80253050
|
T | C | 16 | a0001c0001t0001g0268a0001c0001t0001g0271a0001c0001t0002g0277others(13): Show | 16 | HG01243.hp2 HG01496.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.27+2846A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253050 | ||||||
| chr5:80253205
|
C | T | 4 | a0001c0001t0001g0151a0001c0001t0007g0150a0001c0001t0044g0149others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+2691G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253205 | ||||||
| chr5:80253217
|
T | C | 3 | a0001c0001t0007g0249a0001c0001t0012g0251a0001c0002t0067g0250 | 3 | HG00140.hp1 HG00642.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.27+2679A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253217 | ||||||
| chr5:80253327
|
C | T | 118 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0039others(115): Show | 118 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.27+2569G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253327 | ||||||
| chr5:80253388
|
C | A | 118 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0039others(115): Show | 118 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.27+2508G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253388 | ||||||
| chr5:80253436
|
G | A | 1 | a0001c0001t0041g0279 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27+2460C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253436 | ||||||
| chr5:80253496
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.27+2400G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253496 | ||||||
| chr5:80253497
|
G | A | 9 | a0001c0001t0008g0259a0001c0001t0015g0256a0001c0001t0015g0258others(6): Show | 9 | HG01167.hp2 HG02572.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.27+2399C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253497 | ||||||
| chr5:80253548
|
C | A | 118 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0039others(115): Show | 118 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.27+2348G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253548 | ||||||
| chr5:80253660
|
A | C | 1 | a0001c0002t0027g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.27+2236T>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253660 | ||||||
| chr5:80253780
|
G | A | 118 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0039others(115): Show | 118 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.27+2116C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253780 | ||||||
| chr5:80253828
|
C | T | 2 | a0001c0002t0003g0146a0001c0002t0003g0147 | 2 | NA18942.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.27+2068G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253828 | ||||||
| chr5:80253865
|
C | T | 118 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0039others(115): Show | 118 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.27+2031G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253865 | ||||||
| chr5:80253868
|
G | A | 1 | a0001c0001t0008g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.27+2028C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253868 | ||||||
| chr5:80253895
|
T | C | 3 | a0001c0001t0008g0241a0001c0001t0049g0242a0001c0001t0058g0243 | 3 | HG01891.hp1 HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.27+2001A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253895 | ||||||
| chr5:80253905
|
C | T | 118 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0039others(115): Show | 118 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.27+1991G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253905 | ||||||
| chr5:80253979
|
T | G | 118 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0039others(115): Show | 118 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.27+1917A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253979 | ||||||
| chr5:80253992
|
G | A | 3 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266 | 3 | HG01496.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.27+1904C>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80253992 | ||||||
| chr5:80254191
|
T | C | 4 | a0001c0001t0007g0142a0001c0001t0029g0144a0001c0001t0048g0143others(1): Show | 4 | HG01109.hp1 HG02647.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+1705A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80254191 | ||||||
| chr5:80254229
|
GCTTTT | G | 119 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0039others(116): Show | 119 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.27+1662_27+1666del others(5): Show |
SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80254229 | ||||||
| chr5:80254271
|
C | T | 1 | a0002c0005t0019g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.27+1625G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80254271 | ||||||
| chr5:80254314
|
T | C | 2 | a0001c0001t0011g0245a0001c0001t0026g0244 | 2 | HG00140.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.27+1582A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80254314 | ||||||
| chr5:80254338
|
AG | A | 3 | a0001c0001t0002g0248a0001c0001t0004g0247a0001c0002t0069g0246 | 3 | HG00609.hp2 HG02015.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.27+1557delC | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80254338 | ||||||
| chr5:80254366
|
A | G | 1 | a0001c0002t0003g0041 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.27+1530T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80254366 | ||||||
| chr5:80254402
|
A | G | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(22): Show | 25 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.27+1494T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80254402 | ||||||
| chr5:80254423
|
CT | C | 3 | a0001c0001t0007g0249a0001c0001t0012g0251a0001c0002t0067g0250 | 3 | HG00140.hp1 HG00642.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.27+1472delA | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80254423 | ||||||
| chr5:80254889
|
C | T | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.27+1007G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80254889 | ||||||
| chr5:80254928
|
T | C | 3 | a0001c0001t0007g0249a0001c0001t0012g0251a0001c0002t0067g0250 | 3 | HG00140.hp1 HG00642.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.27+968A>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80254928 | ||||||
| chr5:80255123
|
G | C | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG01496.hp1 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+773C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80255123 | ||||||
| chr5:80255127
|
T | G | 34 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(31): Show | 34 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.27+769A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80255127 | ||||||
| chr5:80255215
|
G | C | 1 | a0001c0001t0037g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.27+681C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80255215 | ||||||
| chr5:80255233
|
G | T | 1 | a0001c0002t0003g0040 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.27+663C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80255233 | ||||||
| chr5:80255287
|
C | A | 1 | a0001c0002t0005g0263 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.27+609G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80255287 | ||||||
| chr5:80255339
|
G | T | 5 | a0001c0001t0001g0268a0001c0001t0008g0267a0001c0001t0010g0266others(2): Show | 5 | HG01496.hp1 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+557C>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80255339 | ||||||
| chr5:80255429
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.27+467T>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80255429 | ||||||
| chr5:80255466
|
T | G | 2 | a0001c0001t0002g0280a0001c0001t0007g0281 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.27+430A>C | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80255466 | ||||||
| chr5:80255556
|
C | T | 1 | a0001c0002t0005g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.27+340G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80255556 | ||||||
| chr5:80255590
|
C | T | 9 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0002t0003g0031others(6): Show | 9 | NA18948.hp2 NA18952.hp2 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.27+306G>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80255590 | ||||||
| chr5:80255592
|
A | T | 1 | a0001c0001t0024g0005 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.27+304T>A | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80255592 | ||||||
| chr5:80255653
|
G | C | 18 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0271others(15): Show | 18 | HG01243.hp2 HG01496.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.27+243C>G | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80255653 | ||||||
| chr5:80255756
|
C | CG | 24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(21): Show | 24 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.27+139dupC | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80255756 | ||||||
| chr5:80255778
|
C | A | 2 | a0001c0001t0004g0282a0001c0001t0062g0283 | 2 | HG01943.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.27+118G>T | SERINC5 | ENSG00000164300.17 | transcript | ENST00000507668.7 | protein_coding | 1/11 | chr5 | 80255778 |