Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 79096 |
|---|---|
| ensemblid | ENSG00000149179.14 |
| hgncid | 28720 |
| symbol | CSTPP1 |
| name | centriolar satellite-associated tubulin polyglutamylase complex regulator 1 |
| refseq_nuc | NM_024113.5 |
| refseq_prot | NP_077018.1 |
| ensembl_nuc | ENST00000278460.12 |
| ensembl_prot | ENSP00000278460.8 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 46936761 |
| end | 47162247 |
| strand | + |
| ver | v1.2 |
| region | chr11:46936761-47162247 |
| region5000 | chr11:46931761-47167247 |
| regionname0 | CSTPP1_chr11_46936761_47162247 |
| regionname5000 | CSTPP1_chr11_46931761_47167247 |
| 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 | 331 | 218 | 70 | 53 | 64 | 4 | 25 | 49 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0002 | 0/0 | 331 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0003 | 0/0 | 331 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0004 | 0/0 | 117 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0005 | 0/0 | 331 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0006 | 0/0 | 331 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| 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 | 996 | 215 | 69 | 52 | 63 | 4 | 25 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| c0002 | 0/0 | 996 | 2 | 1 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| c0003 | 0/0 | 996 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| c0004 | 0/0 | 996 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| c0005 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| c0006 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| c0007 | 0/0 | 996 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| c0008 | 0/0 | 996 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| c0009 | 0/0 | 996 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 655 | 208 | 63 | 48 | 66 | 4 | 25 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| t0002 | 0/0 | 655 | 10 | 8 | 2 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| t0003 | 0/0 | 655 | 5 | 0 | 4 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| t0004 | 0/0 | 655 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| 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 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0022 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0222 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| 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 | 996 | 215 | 69 | 52 | 63 | 4 | 25 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0001c0004 | 0/0 | 996 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0001c0005 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0001c0007 | 0/0 | 996 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0002c0002 | 0/0 | 996 | 2 | 1 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0003c0003 | 0/0 | 996 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0004c0008 | 0/0 | 996 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0005c0006 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0006c0009 | 0/0 | 996 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1650 | 199 | 60 | 46 | 63 | 4 | 24 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0001c0001t0002 | 0/0 | 1650 | 10 | 8 | 2 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0001c0001t0003 | 0/0 | 1650 | 5 | 0 | 4 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0001c0001t0004 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0001c0004t0001 | 0/0 | 1650 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0001c0005t0001 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0001c0007t0001 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0002c0002t0001 | 0/0 | 1650 | 2 | 1 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0003c0003t0001 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0004c0008t0001 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0005c0006t0001 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| a0006c0009t0001 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | copy fasta | chr11 | 46931761 | 47167247 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0022 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0222 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0004t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0005t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0001c0007t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0003c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0004c0008t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0005c0006t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| a0006c0009t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | FIN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | FIN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00609 | hp1 | a0006 | c0009 | t0001 | g0088 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01071 | hp1 | a0001 | c0004 | t0001 | g0111 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0126 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CDX | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02895 | hp2 | a0005 | c0006 | t0001 | g0200 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02965 | hp1 | a0001 | c0005 | t0001 | g0085 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0098 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | STU | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG04184 | hp1 | a0003 | c0003 | t0001 | g0113 | SAS | BEB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | YRI | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18951 | hp1 | a0004 | c0008 | t0001 | g0003 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18991 | hp2 | a0001 | c0007 | t0001 | g0063 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | LWK | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | YRI | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ASW | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ASW | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0087 | AFR | USA | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | USA | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0022 | REF | REF | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0222 | REF | REF | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47052476
|
C | T | 1 | a0006 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.238C>T | p.Arg80Trp | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/9 | 283/1650 | 238/996 | 80/331 | chr11 | 47052476 | ||
| chr11:47052477
|
G | A | 1 | a0003 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.239G>A | p.Arg80Gln | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/9 | 284/1650 | 239/996 | 80/331 | chr11 | 47052477 | ||
| chr11:47137716
|
C | T | 1 | a0004 | 1 | NA18951.hp1 | stop_gained | HIGH | c.352C>T | p.Gln118* | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/9 | 397/1650 | 352/996 | 118/331 | chr11 | 47137716 | ||
| chr11:47161161
|
C | A | 1 | a0002 | 2 | HG01243.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.792C>A | p.Asp264Glu | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 8/9 | 837/1650 | 792/996 | 264/331 | chr11 | 47161161 | ||
| chr11:47161501
|
G | A | 1 | a0005 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.859G>A | p.Ala287Thr | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 9/9 | 904/1650 | 859/996 | 287/331 | chr11 | 47161501 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47137703
|
G | A | 1 | a0001c0004 | 1 | HG01071.hp1 | synonymous_variant | LOW | c.339G>A | p.Pro113Pro | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/9 | 384/1650 | 339/996 | 113/331 | chr11 | 47137703 | ||
| chr11:47157129
|
T | C | 1 | a0001c0005 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.558T>C | p.Pro186Pro | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 6/9 | 603/1650 | 558/996 | 186/331 | chr11 | 47157129 | ||
| chr11:47161623
|
C | T | 1 | a0001c0007 | 1 | NA18991.hp2 | synonymous_variant | LOW | c.981C>T | p.Asp327Asp | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 9/9 | 1026/1650 | 981/996 | 327/331 | chr11 | 47161623 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47161825
|
G | A | 1 | a0001c0001t0003 | 5 | HG01081.hp1 HG01192.hp1 HG01496.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*187G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 9/9 | 187 | chr11 | 47161825 | |||||
| chr11:47162022
|
G | A | 1 | a0001c0001t0002 | 10 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*384G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 9/9 | 384 | chr11 | 47162022 | |||||
| chr11:47162032
|
G | A | 1 | a0001c0001t0004 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*394G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 9/9 | 394 | chr11 | 47162032 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:46937116
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.46+265T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46937116 | ||||||
| chr11:46937147
|
T | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(72): Show | 75 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.46+296T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46937147 | ||||||
| chr11:46937351
|
GT | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(216): Show | 219 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(216): Show |
intron_variant | MODIFIER | c.46+502delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46937351 | |||||
| chr11:46937738
|
C | T | 29 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(26): Show | 29 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.46+887C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46937738 | ||||||
| chr11:46937805
|
T | G | 1 | a0001c0001t0001g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.46+954T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46937805 | ||||||
| chr11:46937820
|
A | T | 1 | a0001c0001t0001g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.46+969A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46937820 | ||||||
| chr11:46937883
|
C | CGTTTT | 6 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(3): Show | 6 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.46+1053_46+1057dup others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46937883 | |||||
| chr11:46938015
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.46+1164C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46938015 | ||||||
| chr11:46938493
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.46+1642C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46938493 | ||||||
| chr11:46938508
|
TC | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(72): Show | 75 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.46+1661delC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46938508 | |||||
| chr11:46938761
|
C | CT | 19 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0173others(16): Show | 19 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.46+1922dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46938761 | |||||
| chr11:46938771
|
T | C | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+1920T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46938771 | ||||||
| chr11:46938771
|
T | TC | 29 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(26): Show | 29 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.46+1920_46+1921ins others(1): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46938771 | ||||||
| chr11:46938780
|
C | CT | 87 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(84): Show | 87 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.46+1944dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46938780 | |||||
| chr11:46938837
|
G | A | 2 | a0002c0002t0001g0086a0002c0002t0001g0087 | 2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.46+1986G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46938837 | ||||||
| chr11:46939011
|
A | C | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.46+2160A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46939011 | ||||||
| chr11:46939082
|
C | CT | 12 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(9): Show | 12 | HG00741.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.46+2256dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939082 | |||||
| chr11:46939082
|
CT | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0074others(7): Show | 10 | HG00609.hp1 HG01074.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+2256delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939082 | |||||
| chr11:46939259
|
T | C | 48 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0173others(45): Show | 48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.46+2408T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46939259 | ||||||
| chr11:46939282
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.46+2431T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46939282 | ||||||
| chr11:46939583
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.46+2732A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46939583 | ||||||
| chr11:46939631
|
C | CATAG | 34 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(31): Show | 34 | HG00609.hp1 HG00609.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.46+2821_46+2824dup others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939631 | |||||
| chr11:46939631
|
C | CATAGATA others(1): Show |
3 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0090 | 3 | HG00621.hp1 HG02165.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.46+2817_46+2824dup others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939631 | |||||
| chr11:46939631
|
CATAG | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0055others(32): Show | 35 | HG01071.hp2 HG01074.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.46+2821_46+2824del others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939631 | |||||
| chr11:46939631
|
CATAGATA others(1): Show |
C | 4 | a0001c0001t0001g0067a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG00735.hp2 HG03516.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+2817_46+2824del others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939631 | |||||
| chr11:46939631
|
CATAGATA others(5): Show |
C | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.46+2813_46+2824del others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939631 | |||||
| chr11:46939668
|
ATAGATAG others(1): Show |
A | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0002c0002t0001g0087 | 3 | HG01358.hp2 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.46+2823_46+2830del others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939668 | |||||
| chr11:46939672
|
ATAGG | A | 53 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(50): Show | 53 | HG00438.hp1 HG00597.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.46+2825_46+2828del others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939672 | |||||
| chr11:46939676
|
G | A | 41 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(38): Show | 41 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.46+2825G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46939676 | ||||||
| chr11:46939831
|
A | AT | 3 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.46+2983dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939831 | |||||
| chr11:46940208
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.46+3357G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46940208 | ||||||
| chr11:46940444
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(2): Show | 5 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+3593T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46940444 | ||||||
| chr11:46940635
|
C | CTA | 3 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.46+3793_46+3794dup others(2): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46940635 | |||||
| chr11:46940684
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.46+3833G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46940684 | ||||||
| chr11:46940736
|
T | G | 1 | a0001c0001t0001g0017 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.46+3885T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46940736 | ||||||
| chr11:46940900
|
T | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(64): Show | 67 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.46+4049T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46940900 | ||||||
| chr11:46940923
|
G | T | 53 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(50): Show | 53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.46+4072G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46940923 | ||||||
| chr11:46941485
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.46+4634A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46941485 | ||||||
| chr11:46941645
|
A | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(162): Show | 165 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.46+4794A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46941645 | ||||||
| chr11:46942496
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.46+5645G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46942496 | ||||||
| chr11:46942520
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.46+5669A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46942520 | ||||||
| chr11:46942609
|
C | T | 48 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0173others(45): Show | 48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.46+5758C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46942609 | ||||||
| chr11:46942800
|
T | C | 4 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 4 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+5949T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46942800 | ||||||
| chr11:46943283
|
C | G | 48 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0173others(45): Show | 48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.46+6432C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46943283 | ||||||
| chr11:46943760
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.46+6909C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46943760 | ||||||
| chr11:46943920
|
C | T | 29 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(26): Show | 29 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.46+7069C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46943920 | ||||||
| chr11:46943975
|
C | T | 90 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(87): Show | 90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.46+7124C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46943975 | ||||||
| chr11:46944179
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(72): Show | 75 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.46+7328G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46944179 | ||||||
| chr11:46944317
|
C | CA | 49 | a0001c0001t0001g0018a0001c0001t0001g0054a0001c0001t0001g0067others(46): Show | 49 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.46+7485dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46944317 | |||||
| chr11:46944405
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.46+7554A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46944405 | ||||||
| chr11:46944662
|
C | A | 1 | a0001c0005t0001g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.46+7811C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46944662 | ||||||
| chr11:46944800
|
T | C | 1 | a0001c0001t0002g0217 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.46+7949T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46944800 | ||||||
| chr11:46944942
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.46+8091A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46944942 | ||||||
| chr11:46945082
|
T | C | 3 | a0001c0001t0001g0055a0001c0001t0001g0067a0001c0001t0001g0074 | 3 | HG00735.hp2 HG01257.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.46+8231T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945082 | ||||||
| chr11:46945218
|
A | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0214 | 2 | HG01261.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.46+8367A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945218 | ||||||
| chr11:46945257
|
G | A | 14 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0108others(11): Show | 14 | HG00609.hp1 HG01071.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.46+8406G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945257 | ||||||
| chr11:46945353
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(72): Show | 75 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.46+8502G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945353 | ||||||
| chr11:46945354
|
C | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.46+8503C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945354 | ||||||
| chr11:46945412
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0165 | 2 | HG00738.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.46+8561C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945412 | ||||||
| chr11:46945530
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.46+8679G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945530 | ||||||
| chr11:46945593
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.46+8742C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945593 | ||||||
| chr11:46945864
|
T | G | 57 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(54): Show | 57 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.46+9013T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945864 | ||||||
| chr11:46946058
|
T | C | 29 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(26): Show | 29 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.46+9207T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46946058 | ||||||
| chr11:46946111
|
C | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.46+9260C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46946111 | ||||||
| chr11:46946128
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.46+9277C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46946128 | ||||||
| chr11:46946159
|
G | T | 1 | a0001c0001t0001g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.46+9308G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46946159 | ||||||
| chr11:46946336
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.46+9485C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46946336 | ||||||
| chr11:46946350
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.46+9499G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46946350 | ||||||
| chr11:46946455
|
G | A | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+9604G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46946455 | ||||||
| chr11:46947131
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(220): Show | 223 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.46+10280T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46947131 | ||||||
| chr11:46947272
|
C | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0006c0009t0001g0088 | 3 | HG00609.hp1 NA18971.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.46+10421C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46947272 | ||||||
| chr11:46947730
|
C | G | 57 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(54): Show | 57 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.46+10879C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46947730 | ||||||
| chr11:46947737
|
C | T | 29 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(26): Show | 29 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.46+10886C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46947737 | ||||||
| chr11:46947928
|
C | CT | 17 | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0001t0001g0043others(14): Show | 17 | HG00438.hp2 HG00597.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.46+11088dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46947928 | |||||
| chr11:46948065
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.46+11214T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46948065 | ||||||
| chr11:46948217
|
G | A | 3 | a0001c0001t0001g0089a0001c0001t0001g0131a0001c0001t0001g0163 | 3 | HG03942.hp1 NA18983.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.46+11366G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46948217 | ||||||
| chr11:46948348
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0064 | 2 | HG01261.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.46+11497G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46948348 | ||||||
| chr11:46948880
|
A | G | 1 | a0001c0001t0003g0126 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.46+12029A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46948880 | ||||||
| chr11:46948931
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.46+12080G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46948931 | ||||||
| chr11:46949025
|
A | T | 1 | a0001c0001t0001g0160 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.46+12174A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46949025 | ||||||
| chr11:46949343
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.46+12492C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46949343 | ||||||
| chr11:46949415
|
C | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.46+12564C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46949415 | ||||||
| chr11:46949669
|
C | CT | 49 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0075others(46): Show | 49 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.46+12834dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46949669 | |||||
| chr11:46949669
|
CT | C | 26 | a0001c0001t0001g0116a0001c0001t0001g0191a0001c0001t0001g0192others(23): Show | 26 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.46+12834delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46949669 | |||||
| chr11:46949888
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.46+13037G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46949888 | ||||||
| chr11:46949889
|
T | G | 1 | a0001c0001t0003g0126 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.46+13038T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46949889 | ||||||
| chr11:46949920
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46+13069G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46949920 | ||||||
| chr11:46949988
|
T | C | 90 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(87): Show | 90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.46+13137T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46949988 | ||||||
| chr11:46950176
|
C | CT | 49 | a0001c0001t0001g0076a0001c0001t0001g0157a0001c0001t0001g0158others(46): Show | 49 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.46+13340dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46950176 | |||||
| chr11:46950229
|
A | G | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+13378A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950229 | ||||||
| chr11:46950235
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.46+13384G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950235 | ||||||
| chr11:46950318
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.46+13467C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950318 | ||||||
| chr11:46950363
|
C | T | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0219 | 3 | HG03516.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.46+13512C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950363 | ||||||
| chr11:46950394
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.46+13543C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950394 | ||||||
| chr11:46950614
|
C | T | 53 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(50): Show | 53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.46+13763C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950614 | ||||||
| chr11:46950824
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.46+13973C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950824 | ||||||
| chr11:46950867
|
G | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.46+14016G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950867 | ||||||
| chr11:46950905
|
C | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.46+14054C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950905 | ||||||
| chr11:46951295
|
CT | C | 46 | a0001c0001t0001g0011a0001c0001t0001g0056a0001c0001t0001g0076others(43): Show | 46 | HG01109.hp1 HG01109.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.46+14463delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46951295 | |||||
| chr11:46951474
|
CTTTG | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0052a0001c0001t0001g0054others(2): Show | 5 | HG01074.hp1 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+14630_46+14633d others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46951474 | |||||
| chr11:46951564
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.46+14713C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46951564 | ||||||
| chr11:46951906
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.46+15055C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46951906 | ||||||
| chr11:46952250
|
G | A | 3 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.46+15399G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46952250 | ||||||
| chr11:46952794
|
C | T | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.46+15943C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46952794 | ||||||
| chr11:46953093
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.46+16242A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46953093 | ||||||
| chr11:46953558
|
A | C | 1 | a0001c0001t0001g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.46+16707A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46953558 | ||||||
| chr11:46953574
|
T | C | 90 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(87): Show | 90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.46+16723T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46953574 | ||||||
| chr11:46953836
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(162): Show | 165 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.46+16985G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46953836 | ||||||
| chr11:46954206
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46+17355T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46954206 | ||||||
| chr11:46954434
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.46+17583G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46954434 | ||||||
| chr11:46954497
|
C | T | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+17646C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46954497 | ||||||
| chr11:46954556
|
T | A | 1 | a0001c0001t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.46+17705T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46954556 | ||||||
| chr11:46954565
|
A | G | 90 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(87): Show | 90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.46+17714A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46954565 | ||||||
| chr11:46954798
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.46+17947C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46954798 | ||||||
| chr11:46954802
|
C | A | 1 | a0001c0001t0001g0166 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.46+17951C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46954802 | ||||||
| chr11:46955310
|
G | T | 58 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(55): Show | 58 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.46+18459G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955310 | ||||||
| chr11:46955347
|
G | GT | 5 | a0001c0001t0001g0061a0001c0001t0001g0081a0001c0001t0001g0128others(2): Show | 5 | HG00735.hp1 HG01981.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+18506dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46955347 | |||||
| chr11:46955369
|
G | T | 10 | a0001c0001t0002g0196a0001c0001t0002g0199a0001c0001t0002g0205others(7): Show | 10 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+18518G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955369 | ||||||
| chr11:46955390
|
G | A | 156 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(153): Show | 156 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(153): Show |
intron_variant | MODIFIER | c.46+18539G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955390 | ||||||
| chr11:46955450
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0186 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.46+18599G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955450 | ||||||
| chr11:46955475
|
C | T | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.46+18624C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955475 | ||||||
| chr11:46955516
|
A | C | 2 | a0001c0001t0001g0179a0001c0001t0001g0186 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.46+18665A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955516 | ||||||
| chr11:46955609
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.46+18758C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955609 | ||||||
| chr11:46955739
|
C | G | 1 | a0001c0001t0001g0103 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.46+18888C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955739 | ||||||
| chr11:46955857
|
C | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0052others(7): Show | 10 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.46+19006C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955857 | ||||||
| chr11:46955858
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.46+19007G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955858 | ||||||
| chr11:46955986
|
A | AC | 15 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(12): Show | 15 | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.46+19148dupC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46955986 | |||||
| chr11:46955986
|
AC | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(117): Show | 120 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.46+19148delC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46955986 | |||||
| chr11:46955986
|
ACC | A | 34 | a0001c0001t0001g0022a0001c0001t0001g0056a0001c0001t0001g0069others(31): Show | 34 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.46+19147_46+19148d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46955986 | |||||
| chr11:46955990
|
C | A | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0184others(1): Show | 4 | HG00609.hp1 HG01243.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+19139C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955990 | ||||||
| chr11:46955991
|
C | A | 2 | a0001c0001t0001g0042a0001c0001t0002g0217 | 2 | HG02145.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.46+19140C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955991 | ||||||
| chr11:46955994
|
C | A | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.46+19143C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955994 | ||||||
| chr11:46955994
|
C | G | 3 | a0001c0001t0001g0083a0001c0001t0001g0135a0001c0001t0001g0169 | 3 | HG03017.hp2 NA18960.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.46+19143C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955994 | ||||||
| chr11:46955995
|
C | A | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+19144C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955995 | ||||||
| chr11:46956118
|
A | C | 1 | a0001c0001t0001g0104 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.46+19267A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46956118 | ||||||
| chr11:46956144
|
T | G | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.46+19293T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46956144 | ||||||
| chr11:46956331
|
A | C | 58 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(55): Show | 58 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.46+19480A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46956331 | ||||||
| chr11:46956371
|
A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0052a0001c0001t0001g0054others(2): Show | 5 | HG01074.hp1 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+19520A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46956371 | ||||||
| chr11:46956553
|
A | G | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+19702A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46956553 | ||||||
| chr11:46956676
|
A | AT | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.46+19834dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46956676 | |||||
| chr11:46957024
|
G | T | 1 | a0001c0001t0001g0020 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.46+20173G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957024 | ||||||
| chr11:46957147
|
G | A | 148 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.46+20296G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957147 | ||||||
| chr11:46957344
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.46+20493C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957344 | ||||||
| chr11:46957472
|
A | G | 148 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.46+20621A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957472 | ||||||
| chr11:46957547
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.46+20696T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957547 | ||||||
| chr11:46957587
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.46+20736A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957587 | ||||||
| chr11:46957837
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.46+20986C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957837 | ||||||
| chr11:46957879
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0101 | 2 | NA18973.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.46+21028C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957879 | ||||||
| chr11:46957914
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.46+21063G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957914 | ||||||
| chr11:46957937
|
T | C | 48 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0173others(45): Show | 48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.46+21086T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957937 | ||||||
| chr11:46958143
|
G | C | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.46+21292G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46958143 | ||||||
| chr11:46958397
|
G | A | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+21546G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46958397 | ||||||
| chr11:46958535
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.46+21684C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46958535 | ||||||
| chr11:46958753
|
CT | C | 90 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(87): Show | 90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.46+21904delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46958753 | |||||
| chr11:46958885
|
C | T | 1 | a0001c0001t0004g0220 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.46+22034C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46958885 | ||||||
| chr11:46958952
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.46+22101A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46958952 | ||||||
| chr11:46959202
|
G | GT | 6 | a0001c0001t0001g0041a0001c0001t0001g0073a0001c0001t0001g0081others(3): Show | 6 | HG02293.hp1 HG02293.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.46+22362dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46959202 | |||||
| chr11:46959588
|
C | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0134 | 3 | NA18949.hp1 NA18977.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.46+22737C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46959588 | ||||||
| chr11:46959641
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.46+22790T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46959641 | ||||||
| chr11:46959865
|
A | AT | 50 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0119others(47): Show | 50 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(47): Show |
intron_variant | MODIFIER | c.46+23033dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46959865 | |||||
| chr11:46959865
|
AT | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0042a0001c0001t0001g0090others(2): Show | 5 | HG00738.hp1 NA18960.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+23033delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46959865 | |||||
| chr11:46960095
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(163): Show | 166 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.46+23244A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960095 | ||||||
| chr11:46960587
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.46+23736G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960587 | ||||||
| chr11:46960612
|
A | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0052others(7): Show | 10 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.46+23761A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960612 | ||||||
| chr11:46960724
|
T | C | 148 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.46+23873T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960724 | ||||||
| chr11:46960861
|
G | A | 10 | a0001c0001t0002g0196a0001c0001t0002g0199a0001c0001t0002g0205others(7): Show | 10 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+24010G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960861 | ||||||
| chr11:46960861
|
GA | G | 43 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(40): Show | 43 | HG01109.hp1 HG01243.hp1 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.46+24021delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46960861 | |||||
| chr11:46960862
|
A | G | 10 | a0001c0001t0002g0196a0001c0001t0002g0199a0001c0001t0002g0205others(7): Show | 10 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+24011A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960862 | ||||||
| chr11:46960911
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.46+24060C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960911 | ||||||
| chr11:46960930
|
G | A | 148 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.46+24079G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960930 | ||||||
| chr11:46960965
|
C | T | 4 | a0001c0001t0001g0039a0001c0001t0001g0056a0001c0001t0001g0059others(1): Show | 4 | HG00280.hp1 HG01071.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+24114C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960965 | ||||||
| chr11:46961009
|
T | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0135 | 2 | NA18960.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.46+24158T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46961009 | ||||||
| chr11:46961227
|
CTTG | C | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+24386_46+24388d others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46961227 | |||||
| chr11:46961687
|
A | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0052others(7): Show | 10 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.46+24836A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46961687 | ||||||
| chr11:46961708
|
T | C | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+24857T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46961708 | ||||||
| chr11:46962089
|
A | G | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-25119A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46962089 | ||||||
| chr11:46962130
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0135 | 2 | NA18960.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.47-25078C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46962130 | ||||||
| chr11:46962303
|
CT | C | 2 | a0001c0001t0002g0205a0001c0001t0002g0218 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.47-24903delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46962303 | |||||
| chr11:46962571
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.47-24637G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46962571 | ||||||
| chr11:46962616
|
C | G | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-24592C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46962616 | ||||||
| chr11:46962770
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.47-24438T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46962770 | ||||||
| chr11:46962935
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.47-24273C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46962935 | ||||||
| chr11:46963078
|
C | T | 90 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(87): Show | 90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.47-24130C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46963078 | ||||||
| chr11:46963106
|
AT | A | 17 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0102others(14): Show | 17 | HG00609.hp1 HG00738.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.47-24092delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46963106 | |||||
| chr11:46963252
|
A | G | 155 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(152): Show | 155 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.47-23956A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46963252 | ||||||
| chr11:46963324
|
CT | C | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-23869delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46963324 | |||||
| chr11:46963558
|
C | T | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.47-23650C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46963558 | ||||||
| chr11:46963628
|
C | CA | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-23572dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46963628 | |||||
| chr11:46963679
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.47-23529G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46963679 | ||||||
| chr11:46963724
|
G | C | 1 | a0001c0001t0001g0165 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.47-23484G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46963724 | ||||||
| chr11:46963784
|
C | CA | 35 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0001g0172others(32): Show | 35 | HG01109.hp1 HG01243.hp1 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.47-23408dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46963784 | |||||
| chr11:46964148
|
C | G | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.47-23060C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46964148 | ||||||
| chr11:46964289
|
CT | C | 50 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(47): Show | 50 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.47-22905delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46964289 | |||||
| chr11:46964291
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.47-22917T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46964291 | ||||||
| chr11:46964386
|
C | G | 29 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(26): Show | 29 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.47-22822C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46964386 | ||||||
| chr11:46964510
|
C | A | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.47-22698C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46964510 | ||||||
| chr11:46964576
|
C | T | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-22632C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46964576 | ||||||
| chr11:46964887
|
G | A | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.47-22321G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46964887 | ||||||
| chr11:46965220
|
C | CT | 13 | a0001c0001t0001g0083a0001c0001t0001g0092a0001c0001t0001g0104others(10): Show | 13 | HG00673.hp1 HG01192.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.47-21976dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46965220 | |||||
| chr11:46965231
|
TTA | T | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.47-21975_47-21974d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46965231 | |||||
| chr11:46965232
|
TA | T | 41 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(38): Show | 41 | HG00280.hp2 HG01109.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.47-21975delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46965232 | ||||||
| chr11:46965233
|
A | T | 89 | a0001c0001t0001g0077a0001c0001t0001g0082a0001c0001t0001g0083others(86): Show | 89 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.47-21975A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46965233 | ||||||
| chr11:46965367
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.47-21841G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46965367 | ||||||
| chr11:46965424
|
C | T | 17 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0094others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.47-21784C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46965424 | ||||||
| chr11:46965444
|
T | C | 53 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(50): Show | 53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.47-21764T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46965444 | ||||||
| chr11:46965848
|
G | A | 29 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(26): Show | 29 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.47-21360G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46965848 | ||||||
| chr11:46965936
|
A | C | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-21272A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46965936 | ||||||
| chr11:46966135
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.47-21073C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46966135 | ||||||
| chr11:46966150
|
C | G | 90 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(87): Show | 90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.47-21058C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46966150 | ||||||
| chr11:46966153
|
C | T | 48 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(45): Show | 48 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.47-21055C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46966153 | ||||||
| chr11:46966292
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.47-20916C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46966292 | ||||||
| chr11:46966299
|
C | G | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-20909C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46966299 | ||||||
| chr11:46966402
|
T | A | 1 | a0001c0001t0001g0024 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.47-20806T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46966402 | ||||||
| chr11:46966429
|
G | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-20779G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46966429 | ||||||
| chr11:46966645
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.47-20563G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46966645 | ||||||
| chr11:46967000
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.47-20208A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46967000 | ||||||
| chr11:46967282
|
T | C | 2 | a0001c0001t0001g0192a0005c0006t0001g0200 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.47-19926T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46967282 | ||||||
| chr11:46967432
|
A | C | 91 | a0001c0001t0001g0037a0001c0001t0001g0082a0001c0001t0001g0083others(88): Show | 91 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.47-19776A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46967432 | ||||||
| chr11:46967466
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.47-19742A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46967466 | ||||||
| chr11:46967831
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.47-19377C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46967831 | ||||||
| chr11:46967945
|
C | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.47-19263C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46967945 | ||||||
| chr11:46968282
|
G | C | 2 | a0001c0001t0001g0192a0005c0006t0001g0200 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.47-18926G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46968282 | ||||||
| chr11:46968789
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-18419C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46968789 | ||||||
| chr11:46968813
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.47-18395C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46968813 | ||||||
| chr11:46968815
|
C | G | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.47-18393C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46968815 | ||||||
| chr11:46968911
|
A | T | 17 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0094others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.47-18297A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46968911 | ||||||
| chr11:46968913
|
A | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0134 | 3 | NA18949.hp1 NA18977.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.47-18295A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46968913 | ||||||
| chr11:46969036
|
C | T | 90 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(87): Show | 90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.47-18172C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46969036 | ||||||
| chr11:46969074
|
A | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0153 | 2 | HG00738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.47-18134A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46969074 | ||||||
| chr11:46969103
|
T | A | 1 | a0001c0001t0001g0132 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.47-18105T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46969103 | ||||||
| chr11:46969144
|
C | A | 8 | a0001c0001t0001g0095a0001c0001t0001g0101a0001c0001t0001g0116others(5): Show | 8 | HG00621.hp2 HG02080.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.47-18064C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46969144 | ||||||
| chr11:46969152
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.47-18056C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46969152 | ||||||
| chr11:46969656
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | HG01099.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.47-17552G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46969656 | ||||||
| chr11:46969693
|
T | A | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-17515T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46969693 | ||||||
| chr11:46970011
|
A | G | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-17197A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46970011 | ||||||
| chr11:46970064
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.47-17144T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46970064 | ||||||
| chr11:46970257
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0170others(1): Show | 4 | HG01071.hp1 HG01515.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-16951C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46970257 | ||||||
| chr11:46970271
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47-16937C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46970271 | ||||||
| chr11:46970402
|
T | TAATA | 6 | a0001c0001t0001g0144a0001c0001t0001g0221a0001c0001t0001g0223others(3): Show | 6 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.47-16779_47-16776d others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46970402 | |||||
| chr11:46971221
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.47-15987C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46971221 | ||||||
| chr11:46971243
|
T | G | 1 | a0001c0001t0001g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.47-15965T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46971243 | ||||||
| chr11:46971257
|
G | T | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-15951G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46971257 | ||||||
| chr11:46971279
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.47-15929T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46971279 | ||||||
| chr11:46971493
|
T | C | 1 | a0001c0001t0001g0042 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.47-15715T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46971493 | ||||||
| chr11:46971644
|
AT | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(8): Show | 11 | HG00642.hp2 HG00733.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.47-15552delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46971644 | |||||
| chr11:46971921
|
A | G | 53 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(50): Show | 53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.47-15287A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46971921 | ||||||
| chr11:46972634
|
C | G | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-14574C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46972634 | ||||||
| chr11:46972728
|
C | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0064 | 2 | HG01261.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.47-14480C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46972728 | ||||||
| chr11:46973163
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.47-14045A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46973163 | ||||||
| chr11:46973242
|
G | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-13966G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46973242 | ||||||
| chr11:46973448
|
C | G | 1 | a0001c0001t0001g0039 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.47-13760C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46973448 | ||||||
| chr11:46973755
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.47-13453C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46973755 | ||||||
| chr11:46973780
|
A | ATGTGTG | 72 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(69): Show | 72 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.47-13414_47-13409d others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46973780 | |||||
| chr11:46973780
|
A | ATGTGTGT others(3): Show |
78 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(75): Show | 78 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(75): Show |
intron_variant | MODIFIER | c.47-13418_47-13409d others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46973780 | |||||
| chr11:46973780
|
A | ATGTGTGT others(5): Show |
10 | a0001c0001t0001g0081a0001c0001t0001g0094a0001c0001t0001g0132others(7): Show | 10 | HG00642.hp1 HG01081.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.47-13420_47-13409d others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46973780 | |||||
| chr11:46973780
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0004g0220 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47-13422_47-13409d others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46973780 | |||||
| chr11:46973780
|
A | ATGTGTGT others(11): Show |
2 | a0001c0001t0001g0221a0001c0005t0001g0085 | 2 | HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.47-13426_47-13409d others(20): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46973780 | |||||
| chr11:46973780
|
A | ATGTGTGT others(13): Show |
2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.47-13409_47-13408i others(22): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46973780 | |||||
| chr11:46974266
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.47-12942G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46974266 | ||||||
| chr11:46974298
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.47-12910C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46974298 | ||||||
| chr11:46974514
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.47-12694G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46974514 | ||||||
| chr11:46974526
|
C | CA | 78 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(75): Show | 78 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.47-12666dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974526 | |||||
| chr11:46974526
|
C | CAA | 19 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0094others(16): Show | 19 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.47-12667_47-12666d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974526 | |||||
| chr11:46974526
|
CA | C | 30 | a0001c0001t0001g0178a0001c0001t0001g0191a0001c0001t0001g0192others(27): Show | 30 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.47-12666delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974526 | |||||
| chr11:46974568
|
T | C | 58 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(55): Show | 58 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.47-12640T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46974568 | ||||||
| chr11:46974593
|
C | T | 17 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0094others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.47-12615C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46974593 | ||||||
| chr11:46974837
|
A | C | 1 | a0001c0001t0001g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.47-12371A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46974837 | ||||||
| chr11:46974857
|
A | AAC | 23 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0022others(20): Show | 23 | HG00280.hp1 HG00438.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.47-12305_47-12304d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974857 | |||||
| chr11:46974857
|
A | AACAC | 8 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0058others(5): Show | 8 | HG01192.hp2 HG03831.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.47-12307_47-12304d others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974857 | |||||
| chr11:46974857
|
AAC | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0055others(3): Show | 6 | HG00735.hp2 HG01257.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.47-12305_47-12304d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974857 | |||||
| chr11:46974857
|
AACAC | A | 10 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(7): Show | 10 | HG01074.hp1 HG01261.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.47-12307_47-12304d others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974857 | |||||
| chr11:46974857
|
AACACACA others(1): Show |
A | 5 | a0001c0001t0001g0014a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02723.hp2 HG03130.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-12311_47-12304d others(10): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974857 | |||||
| chr11:46974857
|
AACACACA others(3): Show |
A | 16 | a0001c0001t0001g0077a0001c0001t0001g0081a0001c0001t0001g0094others(13): Show | 16 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.47-12313_47-12304d others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974857 | |||||
| chr11:46974857
|
AACACACA others(5): Show |
A | 38 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0107others(35): Show | 38 | HG01109.hp2 HG01243.hp2 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.47-12315_47-12304d others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974857 | |||||
| chr11:46974857
|
AACACACA others(7): Show |
A | 89 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(86): Show | 89 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.47-12317_47-12304d others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974857 | |||||
| chr11:46974892
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.47-12316A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46974892 | ||||||
| chr11:46974893
|
C | T | 2 | a0001c0001t0001g0110a0001c0004t0001g0111 | 2 | HG01071.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.47-12315C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46974893 | ||||||
| chr11:46975047
|
G | GC | 90 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(87): Show | 90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.47-12160dupC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46975047 | |||||
| chr11:46975049
|
T | C | 90 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(87): Show | 90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.47-12159T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46975049 | ||||||
| chr11:46975657
|
G | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.47-11551G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46975657 | ||||||
| chr11:46975676
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.47-11532T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46975676 | ||||||
| chr11:46975919
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.47-11289G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46975919 | ||||||
| chr11:46976100
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.47-11108G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46976100 | ||||||
| chr11:46976393
|
T | TCA | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(66): Show | 69 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.47-10786_47-10785d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46976393 | |||||
| chr11:46976393
|
T | TCACA | 8 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0036others(5): Show | 8 | HG00741.hp1 HG02280.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.47-10788_47-10785d others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46976393 | |||||
| chr11:46976393
|
TCA | T | 28 | a0001c0001t0001g0051a0001c0001t0001g0077a0001c0001t0001g0084others(25): Show | 28 | HG00438.hp1 HG01109.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.47-10786_47-10785d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46976393 | |||||
| chr11:46976393
|
TCACA | T | 100 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(97): Show | 100 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.47-10788_47-10785d others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46976393 | |||||
| chr11:46976393
|
TCACACA | T | 12 | a0001c0001t0001g0076a0001c0001t0001g0143a0001c0001t0001g0174others(9): Show | 12 | HG01975.hp2 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.47-10790_47-10785d others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46976393 | |||||
| chr11:46976393
|
TCACACAC others(1): Show |
T | 2 | a0001c0001t0001g0095a0001c0001t0001g0101 | 2 | NA18973.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.47-10792_47-10785d others(10): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46976393 | |||||
| chr11:46976626
|
A | C | 1 | a0001c0001t0001g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.47-10582A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46976626 | ||||||
| chr11:46976718
|
TATGCAGT others(5): Show |
T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.47-10486_47-10475d others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46976718 | |||||
| chr11:46976936
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.47-10272G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46976936 | ||||||
| chr11:46976961
|
T | C | 155 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(152): Show | 155 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.47-10247T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46976961 | ||||||
| chr11:46977305
|
C | T | 1 | a0001c0007t0001g0063 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.47-9903C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46977305 | ||||||
| chr11:46977364
|
T | C | 7 | a0001c0001t0001g0095a0001c0001t0001g0101a0001c0001t0001g0116others(4): Show | 7 | HG00621.hp2 HG02080.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-9844T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46977364 | ||||||
| chr11:46977396
|
T | A | 25 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0095others(22): Show | 25 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.47-9812T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46977396 | ||||||
| chr11:46977469
|
T | C | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-9739T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46977469 | ||||||
| chr11:46978287
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.47-8921G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46978287 | ||||||
| chr11:46978464
|
T | A | 1 | a0001c0001t0001g0025 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.47-8744T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46978464 | ||||||
| chr11:46978470
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.47-8738G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46978470 | ||||||
| chr11:46978671
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.47-8537T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46978671 | ||||||
| chr11:46979023
|
A | T | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.47-8185A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46979023 | ||||||
| chr11:46979387
|
C | T | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.47-7821C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46979387 | ||||||
| chr11:46979660
|
C | T | 46 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0084others(43): Show | 46 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.47-7548C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46979660 | ||||||
| chr11:46979863
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.47-7345C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46979863 | ||||||
| chr11:46980081
|
A | C | 54 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(51): Show | 54 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.47-7127A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46980081 | ||||||
| chr11:46980084
|
A | C | 1 | a0001c0001t0001g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.47-7124A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46980084 | ||||||
| chr11:46980357
|
C | G | 72 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(69): Show | 72 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.47-6851C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46980357 | ||||||
| chr11:46980454
|
C | A | 90 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(87): Show | 90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.47-6754C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46980454 | ||||||
| chr11:46980606
|
C | G | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.47-6602C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46980606 | ||||||
| chr11:46981021
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.47-6187G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981021 | ||||||
| chr11:46981063
|
A | T | 148 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.47-6145A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981063 | ||||||
| chr11:46981335
|
A | C | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-5873A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981335 | ||||||
| chr11:46981638
|
T | TTTTTGAG others(6): Show |
1 | a0001c0001t0001g0021 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.47-5570_47-5569ins others(13): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981638 | ||||||
| chr11:46981639
|
G | T | 1 | a0001c0001t0001g0021 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.47-5569G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981639 | ||||||
| chr11:46981692
|
T | G | 26 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(23): Show | 26 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.47-5516T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981692 | ||||||
| chr11:46981730
|
G | A | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-5478G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981730 | ||||||
| chr11:46981753
|
G | A | 90 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(87): Show | 90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.47-5455G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981753 | ||||||
| chr11:46981759
|
A | T | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-5449A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981759 | ||||||
| chr11:46981766
|
T | A | 148 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.47-5442T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981766 | ||||||
| chr11:46982130
|
A | T | 53 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(50): Show | 53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.47-5078A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46982130 | ||||||
| chr11:46982413
|
CTTAG | C | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-4791_47-4788del others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46982413 | |||||
| chr11:46982436
|
T | G | 53 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(50): Show | 53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.47-4772T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46982436 | ||||||
| chr11:46982458
|
A | T | 1 | a0001c0001t0001g0146 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.47-4750A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46982458 | ||||||
| chr11:46982941
|
G | A | 48 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0173others(45): Show | 48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.47-4267G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46982941 | ||||||
| chr11:46983034
|
A | C | 9 | a0001c0001t0002g0196a0001c0001t0002g0199a0001c0001t0002g0205others(6): Show | 9 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.47-4174A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46983034 | ||||||
| chr11:46983034
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(211): Show | 214 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.47-4174A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46983034 | ||||||
| chr11:46983049
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.47-4159A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46983049 | ||||||
| chr11:46983583
|
G | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-3625G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46983583 | ||||||
| chr11:46983817
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.47-3391G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46983817 | ||||||
| chr11:46984082
|
G | A | 48 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0173others(45): Show | 48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.47-3126G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46984082 | ||||||
| chr11:46984517
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.47-2691G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46984517 | ||||||
| chr11:46984586
|
C | CT | 53 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(50): Show | 53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.47-2613dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46984586 | |||||
| chr11:46984880
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.47-2328T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46984880 | ||||||
| chr11:46985051
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.47-2157T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46985051 | ||||||
| chr11:46985055
|
G | A | 53 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(50): Show | 53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.47-2153G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46985055 | ||||||
| chr11:46985216
|
G | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0183 | 2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.47-1992G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46985216 | ||||||
| chr11:46985220
|
G | A | 48 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0173others(45): Show | 48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.47-1988G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46985220 | ||||||
| chr11:46985242
|
C | T | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-1966C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46985242 | ||||||
| chr11:46985263
|
G | C | 16 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(13): Show | 16 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.47-1945G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46985263 | ||||||
| chr11:46985580
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.47-1628C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46985580 | ||||||
| chr11:46986045
|
A | G | 1 | a0005c0006t0001g0200 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.47-1163A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46986045 | ||||||
| chr11:46986048
|
A | T | 1 | a0001c0001t0001g0127 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.47-1160A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46986048 | ||||||
| chr11:46986153
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.47-1055A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46986153 | ||||||
| chr11:46986370
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.47-838C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46986370 | ||||||
| chr11:46986399
|
A | T | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.47-809A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46986399 | ||||||
| chr11:46986423
|
CT | C | 38 | a0001c0001t0001g0052a0001c0001t0001g0072a0001c0001t0001g0076others(35): Show | 38 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(35): Show |
intron_variant | MODIFIER | c.47-770delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46986423 | |||||
| chr11:46986574
|
C | T | 18 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0094others(15): Show | 18 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.47-634C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46986574 | ||||||
| chr11:46986579
|
C | A | 1 | a0001c0001t0001g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.47-629C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46986579 | ||||||
| chr11:46986828
|
A | G | 97 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(94): Show | 97 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.47-380A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46986828 | ||||||
| chr11:46987490
|
G | GT | 166 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(163): Show | 166 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.149+183dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46987490 | |||||
| chr11:46987773
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.149+463C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46987773 | ||||||
| chr11:46987838
|
ATATAAGG others(3568): Show |
A | 1 | a0001c0001t0001g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.149+530_149+4104de others(1): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46987838 | |||||
| chr11:46987900
|
A | G | 53 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(50): Show | 53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.149+590A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46987900 | ||||||
| chr11:46988309
|
C | T | 29 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(26): Show | 29 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.149+999C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46988309 | ||||||
| chr11:46988613
|
C | CA | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(214): Show | 217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.149+1309dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46988613 | |||||
| chr11:46988823
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+1513A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46988823 | ||||||
| chr11:46988882
|
T | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0221a0001c0001t0001g0223others(3): Show | 6 | HG02559.hp1 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+1572T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46988882 | ||||||
| chr11:46988887
|
T | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.149+1577T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46988887 | ||||||
| chr11:46988940
|
G | A | 18 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(15): Show | 18 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.149+1630G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46988940 | ||||||
| chr11:46989145
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.149+1835G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46989145 | ||||||
| chr11:46989537
|
G | A | 3 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.149+2227G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46989537 | ||||||
| chr11:46989567
|
T | C | 4 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0135others(1): Show | 4 | NA18960.hp2 NA18964.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+2257T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46989567 | ||||||
| chr11:46989878
|
A | G | 154 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(151): Show | 154 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.149+2568A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46989878 | ||||||
| chr11:46990033
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+2723T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46990033 | ||||||
| chr11:46991196
|
GT | G | 132 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(129): Show | 132 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.149+3903delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46991196 | |||||
| chr11:46991376
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.149+4066G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46991376 | ||||||
| chr11:46991803
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.149+4493C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46991803 | ||||||
| chr11:46991834
|
G | A | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+4524G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46991834 | ||||||
| chr11:46991834
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.149+4524G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46991834 | ||||||
| chr11:46991890
|
G | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0052others(7): Show | 10 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+4580G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46991890 | ||||||
| chr11:46991922
|
C | G | 155 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(152): Show | 155 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.149+4612C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46991922 | ||||||
| chr11:46991927
|
GACGGGGT others(80): Show |
G | 1 | a0001c0001t0001g0144 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.149+4619_149+4705d others(89): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46991927 | |||||
| chr11:46991929
|
C | T | 46 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(43): Show | 46 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.149+4619C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46991929 | ||||||
| chr11:46991930
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.149+4620G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46991930 | ||||||
| chr11:46992017
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.149+4707A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46992017 | ||||||
| chr11:46992362
|
A | G | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+5052A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46992362 | ||||||
| chr11:46992384
|
C | A | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+5074C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46992384 | ||||||
| chr11:46992516
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.149+5206G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46992516 | ||||||
| chr11:46992541
|
A | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+5231A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46992541 | ||||||
| chr11:46992629
|
G | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0106a0001c0001t0001g0167 | 3 | HG00738.hp2 HG01358.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.149+5319G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46992629 | ||||||
| chr11:46992665
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0106a0001c0001t0001g0167 | 3 | HG00738.hp2 HG01358.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.149+5355C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46992665 | ||||||
| chr11:46992972
|
G | GT | 53 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(50): Show | 53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.149+5664dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46992972 | |||||
| chr11:46993500
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0008 | 2 | HG00609.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.149+6190G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46993500 | ||||||
| chr11:46993622
|
T | C | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+6312T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46993622 | ||||||
| chr11:46993745
|
G | T | 90 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(87): Show | 90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.149+6435G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46993745 | ||||||
| chr11:46993884
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+6574C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46993884 | ||||||
| chr11:46993951
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.149+6641G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46993951 | ||||||
| chr11:46994000
|
G | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+6690G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46994000 | ||||||
| chr11:46994153
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.149+6843C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46994153 | ||||||
| chr11:46994502
|
T | A | 1 | a0001c0001t0001g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.149+7192T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46994502 | ||||||
| chr11:46995146
|
G | A | 54 | a0001c0001t0001g0064a0001c0001t0001g0076a0001c0001t0001g0077others(51): Show | 54 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.149+7836G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46995146 | ||||||
| chr11:46995588
|
T | TGA | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+8284_149+8285d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46995588 | |||||
| chr11:46995602
|
C | A | 7 | a0001c0001t0001g0121a0001c0001t0001g0133a0001c0001t0001g0141others(4): Show | 7 | HG00738.hp1 HG00741.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+8292C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46995602 | ||||||
| chr11:46995605
|
G | C | 7 | a0001c0001t0001g0121a0001c0001t0001g0133a0001c0001t0001g0141others(4): Show | 7 | HG00738.hp1 HG00741.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+8295G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46995605 | ||||||
| chr11:46995606
|
C | T | 1 | a0001c0001t0001g0022 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.149+8296C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46995606 | ||||||
| chr11:46995652
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.149+8342T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46995652 | ||||||
| chr11:46995778
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.149+8468A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46995778 | ||||||
| chr11:46995960
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.149+8650C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46995960 | ||||||
| chr11:46995974
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.149+8664G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46995974 | ||||||
| chr11:46996080
|
T | C | 2 | a0001c0001t0001g0179a0001c0001t0001g0186 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.149+8770T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996080 | ||||||
| chr11:46996088
|
T | G | 1 | a0001c0001t0003g0097 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.149+8778T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996088 | ||||||
| chr11:46996244
|
G | A | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.149+8934G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996244 | ||||||
| chr11:46996310
|
A | AT | 53 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(50): Show | 53 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.149+9011dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46996310 | |||||
| chr11:46996310
|
AT | A | 57 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(54): Show | 57 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.149+9011delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46996310 | |||||
| chr11:46996316
|
T | A | 4 | a0001c0001t0001g0081a0001c0001t0001g0194a0001c0001t0001g0197others(1): Show | 4 | HG02451.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+9006T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996316 | ||||||
| chr11:46996327
|
G | A | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+9017G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996327 | ||||||
| chr11:46996397
|
G | A | 1 | a0005c0006t0001g0200 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.149+9087G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996397 | ||||||
| chr11:46996453
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.149+9143G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996453 | ||||||
| chr11:46996538
|
G | T | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.149+9228G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996538 | ||||||
| chr11:46996545
|
G | A | 3 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.149+9235G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996545 | ||||||
| chr11:46996829
|
G | A | 1 | a0004c0008t0001g0003 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.149+9519G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996829 | ||||||
| chr11:46996872
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.149+9562G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996872 | ||||||
| chr11:46996920
|
A | G | 1 | a0001c0005t0001g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.149+9610A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996920 | ||||||
| chr11:46996951
|
C | T | 47 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(44): Show | 47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.149+9641C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996951 | ||||||
| chr11:46997240
|
G | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0186 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.149+9930G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46997240 | ||||||
| chr11:46997254
|
C | G | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+9944C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46997254 | ||||||
| chr11:46997424
|
T | C | 53 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(50): Show | 53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.149+10114T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46997424 | ||||||
| chr11:46997844
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.149+10534T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46997844 | ||||||
| chr11:46997873
|
G | A | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+10563G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46997873 | ||||||
| chr11:46997909
|
C | G | 1 | a0001c0001t0001g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.149+10599C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46997909 | ||||||
| chr11:46997971
|
A | G | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+10661A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46997971 | ||||||
| chr11:46998226
|
G | C | 155 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(152): Show | 155 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.149+10916G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46998226 | ||||||
| chr11:46998616
|
A | G | 53 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(50): Show | 53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.149+11306A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46998616 | ||||||
| chr11:46998711
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.149+11401C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46998711 | ||||||
| chr11:46998925
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.149+11615A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46998925 | ||||||
| chr11:46999119
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.149+11809G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46999119 | ||||||
| chr11:46999222
|
AATAATAA others(4): Show |
A | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.149+11921_149+1193 others(15): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46999222 | |||||
| chr11:46999663
|
G | A | 10 | a0001c0001t0002g0196a0001c0001t0002g0199a0001c0001t0002g0205others(7): Show | 10 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.149+12353G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46999663 | ||||||
| chr11:46999896
|
G | A | 53 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(50): Show | 53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.149+12586G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46999896 | ||||||
| chr11:47000750
|
GT | G | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+13441delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47000750 | ||||||
| chr11:47001181
|
T | G | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.149+13871T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47001181 | ||||||
| chr11:47001399
|
T | C | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+14089T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47001399 | ||||||
| chr11:47001476
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+14166G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47001476 | ||||||
| chr11:47002146
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.149+14836C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47002146 | ||||||
| chr11:47002254
|
T | G | 1 | a0001c0001t0001g0154 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.149+14944T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47002254 | ||||||
| chr11:47002628
|
C | G | 1 | a0001c0001t0001g0024 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.149+15318C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47002628 | ||||||
| chr11:47002982
|
T | A | 1 | a0001c0001t0001g0136 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.149+15672T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47002982 | ||||||
| chr11:47003502
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+16192C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47003502 | ||||||
| chr11:47003560
|
CTCAGGAT others(3): Show |
C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+16257_149+1626 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47003560 | |||||
| chr11:47003565
|
G | A | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+16255G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47003565 | ||||||
| chr11:47003960
|
C | G | 1 | a0001c0001t0001g0038 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.149+16650C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47003960 | ||||||
| chr11:47004134
|
TTTGTTG | T | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+16836_149+1684 others(10): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47004134 | |||||
| chr11:47004160
|
GTTTTTGT others(7): Show |
G | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.149+16870_149+1688 others(18): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47004160 | |||||
| chr11:47004343
|
CT | C | 53 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(50): Show | 53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.149+17043delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47004343 | |||||
| chr11:47004525
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.149+17215C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47004525 | ||||||
| chr11:47005148
|
AAG | A | 13 | a0001c0001t0001g0049a0001c0001t0001g0083a0001c0001t0001g0094others(10): Show | 13 | HG00642.hp1 HG01081.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.149+17842_149+1784 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47005148 | |||||
| chr11:47006590
|
CT | C | 10 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(7): Show | 10 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+19292delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47006590 | |||||
| chr11:47006618
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.149+19308T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47006618 | ||||||
| chr11:47006746
|
A | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG02293.hp2 HG02300.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.149+19436A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47006746 | ||||||
| chr11:47006755
|
A | AT | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(21): Show | 24 | HG00642.hp2 HG00735.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.149+19464dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47006755 | |||||
| chr11:47006755
|
A | ATT | 5 | a0001c0001t0001g0073a0001c0001t0001g0090a0001c0001t0001g0135others(2): Show | 5 | HG01192.hp1 NA18960.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+19463_149+1946 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47006755 | |||||
| chr11:47006755
|
A | ATTT | 14 | a0001c0001t0001g0049a0001c0001t0001g0083a0001c0001t0001g0094others(11): Show | 14 | HG00642.hp1 HG01081.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.149+19462_149+1946 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47006755 | |||||
| chr11:47006980
|
C | T | 121 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(118): Show | 121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.149+19670C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47006980 | ||||||
| chr11:47007001
|
G | GT | 73 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0013others(70): Show | 73 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.149+19713dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47007001 | |||||
| chr11:47007001
|
G | GTT | 7 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0081others(4): Show | 7 | HG00438.hp1 HG02293.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+19712_149+1971 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47007001 | |||||
| chr11:47007748
|
G | A | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.149+20438G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47007748 | ||||||
| chr11:47008062
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.149+20752G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47008062 | ||||||
| chr11:47009198
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+21888C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47009198 | ||||||
| chr11:47009551
|
C | A | 1 | a0001c0001t0001g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.149+22241C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47009551 | ||||||
| chr11:47009886
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.149+22576T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47009886 | ||||||
| chr11:47009940
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.149+22630A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47009940 | ||||||
| chr11:47009987
|
A | G | 18 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0102others(15): Show | 18 | HG00609.hp1 HG00738.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.149+22677A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47009987 | ||||||
| chr11:47010085
|
G | T | 5 | a0001c0001t0001g0125a0001c0001t0001g0143a0001c0001t0001g0151others(2): Show | 5 | HG01934.hp1 HG01975.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+22775G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47010085 | ||||||
| chr11:47010387
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+23077C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47010387 | ||||||
| chr11:47010499
|
C | T | 1 | a0001c0001t0002g0207 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.149+23189C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47010499 | ||||||
| chr11:47011218
|
C | A | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.149+23908C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011218 | ||||||
| chr11:47011234
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.149+23924T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011234 | ||||||
| chr11:47011266
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.149+23956T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011266 | ||||||
| chr11:47011320
|
A | C | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+24010A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011320 | ||||||
| chr11:47011343
|
G | A | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+24033G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011343 | ||||||
| chr11:47011346
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.149+24036A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011346 | ||||||
| chr11:47011373
|
A | G | 4 | a0001c0001t0001g0175a0001c0001t0001g0184a0001c0001t0001g0187others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+24063A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011373 | ||||||
| chr11:47011572
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+24262T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011572 | ||||||
| chr11:47011650
|
T | G | 1 | a0001c0001t0001g0156 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.149+24340T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011650 | ||||||
| chr11:47012150
|
A | G | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+24840A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47012150 | ||||||
| chr11:47012528
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.149+25218G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47012528 | ||||||
| chr11:47012683
|
C | T | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+25373C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47012683 | ||||||
| chr11:47012995
|
T | TTA | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.149+25695_149+2569 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47012995 | |||||
| chr11:47013000
|
T | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+25690T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47013000 | ||||||
| chr11:47013006
|
T | TA | 103 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(100): Show | 103 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.149+25696_149+2569 others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47013006 | ||||||
| chr11:47013131
|
G | GCATATAT others(39): Show |
9 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0177others(6): Show | 9 | HG02647.hp1 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.149+25859_149+2590 others(50): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47013131 | |||||
| chr11:47013817
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.149+26507A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47013817 | ||||||
| chr11:47014022
|
A | G | 126 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(123): Show | 126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.149+26712A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47014022 | ||||||
| chr11:47014129
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.149+26819G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47014129 | ||||||
| chr11:47014183
|
A | T | 1 | a0001c0001t0002g0218 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.149+26873A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47014183 | ||||||
| chr11:47014210
|
G | A | 148 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.149+26900G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47014210 | ||||||
| chr11:47014308
|
GAGAA | G | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0219 | 3 | HG03516.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.149+27006_149+2700 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47014308 | |||||
| chr11:47014385
|
GA | G | 76 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(73): Show | 76 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.149+27085delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47014385 | |||||
| chr11:47014954
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.149+27644G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47014954 | ||||||
| chr11:47015116
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.149+27806C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47015116 | ||||||
| chr11:47015243
|
G | C | 148 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.149+27933G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47015243 | ||||||
| chr11:47015304
|
T | TA | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+28006dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47015304 | |||||
| chr11:47015399
|
G | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0052others(7): Show | 10 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+28089G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47015399 | ||||||
| chr11:47015499
|
A | T | 1 | a0001c0001t0001g0154 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.149+28189A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47015499 | ||||||
| chr11:47015553
|
C | T | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.149+28243C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47015553 | ||||||
| chr11:47016255
|
G | A | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.149+28945G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016255 | ||||||
| chr11:47016390
|
C | CA | 6 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0090others(3): Show | 6 | HG01243.hp2 HG01934.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+29086dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47016390 | |||||
| chr11:47016390
|
C | CAA | 10 | a0001c0001t0001g0083a0001c0001t0001g0094a0001c0001t0001g0107others(7): Show | 10 | HG00642.hp1 HG01081.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+29085_149+2908 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47016390 | |||||
| chr11:47016396
|
AC | A | 9 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(6): Show | 9 | HG02572.hp2 HG02615.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.149+29087delC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016396 | ||||||
| chr11:47016397
|
C | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(203): Show | 206 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.149+29087C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016397 | ||||||
| chr11:47016399
|
A | C | 121 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0082others(118): Show | 121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.149+29089A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016399 | ||||||
| chr11:47016400
|
A | C | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+29090A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016400 | ||||||
| chr11:47016401
|
A | C | 1 | a0001c0001t0001g0059 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.149+29091A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016401 | ||||||
| chr11:47016404
|
C | A | 143 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077others(140): Show | 143 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(140): Show |
intron_variant | MODIFIER | c.149+29094C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016404 | ||||||
| chr11:47016410
|
A | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+29100A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016410 | ||||||
| chr11:47016411
|
C | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0107a0001c0001t0001g0132 | 3 | HG02145.hp1 HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.149+29101C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016411 | ||||||
| chr11:47016421
|
A | C | 1 | a0001c0001t0001g0138 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.149+29111A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016421 | ||||||
| chr11:47016515
|
A | G | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.149+29205A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016515 | ||||||
| chr11:47016526
|
G | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.149+29216G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016526 | ||||||
| chr11:47016669
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(163): Show | 166 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.149+29359A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016669 | ||||||
| chr11:47016754
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.149+29444C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016754 | ||||||
| chr11:47016808
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.149+29498C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016808 | ||||||
| chr11:47016839
|
C | CT | 102 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0030others(99): Show | 102 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.149+29550dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47016839 | |||||
| chr11:47016839
|
C | CTT | 10 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(7): Show | 10 | HG02257.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.149+29549_149+2955 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47016839 | |||||
| chr11:47016877
|
C | G | 1 | a0001c0001t0001g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.149+29567C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016877 | ||||||
| chr11:47016978
|
A | G | 126 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(123): Show | 126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.149+29668A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016978 | ||||||
| chr11:47017009
|
A | AT | 5 | a0001c0001t0001g0018a0001c0001t0001g0186a0001c0001t0001g0203others(2): Show | 5 | HG01109.hp2 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+29714dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47017009 | |||||
| chr11:47017173
|
AT | A | 142 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077others(139): Show | 142 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.149+29882delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47017173 | |||||
| chr11:47017203
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.149+29893C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47017203 | ||||||
| chr11:47017235
|
C | T | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.149+29925C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47017235 | ||||||
| chr11:47017238
|
A | G | 3 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.149+29928A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47017238 | ||||||
| chr11:47017656
|
C | G | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.149+30346C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47017656 | ||||||
| chr11:47017667
|
CT | C | 26 | a0001c0001t0001g0011a0001c0001t0001g0058a0001c0001t0001g0072others(23): Show | 26 | HG01192.hp2 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.149+30375delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47017667 | |||||
| chr11:47017667
|
CTT | C | 87 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(84): Show | 87 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.149+30374_149+3037 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47017667 | |||||
| chr11:47017667
|
CTTT | C | 10 | a0001c0001t0001g0191a0001c0001t0001g0201a0001c0001t0001g0202others(7): Show | 10 | HG01261.hp1 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+30373_149+3037 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47017667 | |||||
| chr11:47018287
|
C | CT | 20 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0023others(17): Show | 20 | HG00673.hp2 HG01934.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.149+31002dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47018287 | |||||
| chr11:47018287
|
CT | C | 10 | a0001c0001t0001g0011a0001c0001t0001g0061a0001c0001t0001g0101others(7): Show | 10 | HG00621.hp2 HG01081.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.149+31002delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47018287 | |||||
| chr11:47018460
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.149+31150A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47018460 | ||||||
| chr11:47018483
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.149+31173C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47018483 | ||||||
| chr11:47018528
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+31218C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47018528 | ||||||
| chr11:47018561
|
G | T | 1 | a0001c0001t0001g0170 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.149+31251G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47018561 | ||||||
| chr11:47019030
|
G | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0116others(4): Show | 7 | HG00621.hp2 HG02080.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+31720G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47019030 | ||||||
| chr11:47019153
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0214 | 2 | HG01261.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.149+31843G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47019153 | ||||||
| chr11:47019303
|
A | G | 126 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(123): Show | 126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.149+31993A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47019303 | ||||||
| chr11:47019396
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.149+32086G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47019396 | ||||||
| chr11:47019514
|
G | A | 148 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.149+32204G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47019514 | ||||||
| chr11:47019612
|
A | C | 121 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(118): Show | 121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.149+32302A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47019612 | ||||||
| chr11:47020108
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.150-32280A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47020108 | ||||||
| chr11:47020340
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.150-32048C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47020340 | ||||||
| chr11:47020604
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.150-31784A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47020604 | ||||||
| chr11:47020605
|
CTA | C | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.150-31781_150-3178 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47020605 | |||||
| chr11:47020949
|
A | C | 1 | a0001c0001t0001g0114 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.150-31439A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47020949 | ||||||
| chr11:47021267
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.150-31121G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47021267 | ||||||
| chr11:47021581
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0214 | 2 | HG01261.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.150-30807G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47021581 | ||||||
| chr11:47021682
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.150-30706G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47021682 | ||||||
| chr11:47021903
|
CCCAATGA others(3): Show |
C | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-30483_150-3047 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47021903 | |||||
| chr11:47022004
|
G | C | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.150-30384G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022004 | ||||||
| chr11:47022035
|
G | GT | 8 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0050others(5): Show | 8 | HG01261.hp1 HG01934.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.150-30338dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47022035 | |||||
| chr11:47022155
|
T | TAA | 148 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.150-30231_150-3023 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47022155 | |||||
| chr11:47022273
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.150-30115G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022273 | ||||||
| chr11:47022312
|
C | A | 5 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0137others(2): Show | 5 | HG00438.hp1 NA18947.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-30076C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022312 | ||||||
| chr11:47022358
|
C | CT | 10 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0019others(7): Show | 10 | HG00597.hp1 HG01934.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.150-30002dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47022358 | |||||
| chr11:47022358
|
CT | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(45): Show | 48 | HG00597.hp2 HG00642.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.150-30002delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47022358 | |||||
| chr11:47022358
|
CTT | C | 99 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0089others(96): Show | 99 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.150-30003_150-3000 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47022358 | |||||
| chr11:47022401
|
G | A | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-29987G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022401 | ||||||
| chr11:47022420
|
A | AGTACAGT | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-29966_150-2996 others(11): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47022420 | |||||
| chr11:47022489
|
C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0052a0001c0001t0001g0054others(2): Show | 5 | HG01074.hp1 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-29899C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022489 | ||||||
| chr11:47022515
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.150-29873G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022515 | ||||||
| chr11:47022552
|
T | C | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-29836T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022552 | ||||||
| chr11:47022562
|
G | T | 121 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(118): Show | 121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.150-29826G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022562 | ||||||
| chr11:47022567
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.150-29821A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022567 | ||||||
| chr11:47022571
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.150-29817T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022571 | ||||||
| chr11:47022623
|
G | T | 1 | a0001c0001t0001g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.150-29765G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022623 | ||||||
| chr11:47022693
|
T | C | 2 | a0001c0001t0001g0192a0005c0006t0001g0200 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.150-29695T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022693 | ||||||
| chr11:47022698
|
T | C | 148 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.150-29690T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022698 | ||||||
| chr11:47022804
|
G | A | 148 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.150-29584G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022804 | ||||||
| chr11:47022813
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.150-29575C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022813 | ||||||
| chr11:47023220
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.150-29168G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47023220 | ||||||
| chr11:47023528
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0186 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.150-28860C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47023528 | ||||||
| chr11:47023816
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.150-28572G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47023816 | ||||||
| chr11:47024303
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.150-28085A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47024303 | ||||||
| chr11:47024378
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.150-28010T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47024378 | ||||||
| chr11:47024390
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.150-27998A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47024390 | ||||||
| chr11:47025003
|
G | A | 126 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(123): Show | 126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.150-27385G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47025003 | ||||||
| chr11:47025505
|
A | G | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-26883A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47025505 | ||||||
| chr11:47025508
|
A | G | 148 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.150-26880A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47025508 | ||||||
| chr11:47025569
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0153 | 2 | HG00738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.150-26819G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47025569 | ||||||
| chr11:47025671
|
T | A | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-26717T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47025671 | ||||||
| chr11:47025684
|
G | C | 1 | a0001c0001t0001g0162 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.150-26704G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47025684 | ||||||
| chr11:47025859
|
A | C | 1 | a0001c0001t0001g0054 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.150-26529A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47025859 | ||||||
| chr11:47026440
|
AT | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02723.hp2 HG03130.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-25939delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47026440 | |||||
| chr11:47026464
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.150-25924T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47026464 | ||||||
| chr11:47027149
|
T | TA | 15 | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0001t0001g0043others(12): Show | 15 | HG00438.hp2 HG01361.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.150-25232dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47027149 | |||||
| chr11:47027684
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.150-24704G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47027684 | ||||||
| chr11:47027927
|
C | CT | 130 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(127): Show | 130 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.150-24447dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47027927 | |||||
| chr11:47028072
|
C | T | 3 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.150-24316C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47028072 | ||||||
| chr11:47028108
|
A | G | 5 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0102others(2): Show | 5 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-24280A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47028108 | ||||||
| chr11:47028109
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | HG01099.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.150-24279G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47028109 | ||||||
| chr11:47028649
|
A | G | 3 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.150-23739A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47028649 | ||||||
| chr11:47028671
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.150-23717G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47028671 | ||||||
| chr11:47028759
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.150-23629T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47028759 | ||||||
| chr11:47028772
|
CAA | C | 4 | a0001c0001t0001g0175a0001c0001t0001g0184a0001c0001t0001g0187others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-23614_150-2361 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47028772 | |||||
| chr11:47028846
|
C | CT | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-23533dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47028846 | |||||
| chr11:47028983
|
G | T | 126 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(123): Show | 126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.150-23405G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47028983 | ||||||
| chr11:47029609
|
C | CT | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-22778dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47029609 | |||||
| chr11:47029899
|
A | T | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.150-22489A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47029899 | ||||||
| chr11:47029923
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0153 | 2 | HG00738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.150-22465C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47029923 | ||||||
| chr11:47029937
|
G | GA | 24 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0023others(21): Show | 24 | HG00280.hp1 HG00438.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.150-22436dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47029937 | |||||
| chr11:47029937
|
GA | G | 7 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(4): Show | 7 | HG00597.hp1 HG01081.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.150-22436delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47029937 | |||||
| chr11:47030522
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.150-21866T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47030522 | ||||||
| chr11:47030671
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.150-21717C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47030671 | ||||||
| chr11:47031478
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.150-20910G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47031478 | ||||||
| chr11:47031696
|
CT | C | 17 | a0001c0001t0001g0001a0001c0001t0001g0051a0001c0001t0001g0056others(14): Show | 17 | HG00642.hp1 HG01515.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.150-20673delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47031696 | |||||
| chr11:47031698
|
T | C | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.150-20690T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47031698 | ||||||
| chr11:47031715
|
T | A | 134 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(131): Show | 134 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.150-20673T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47031715 | ||||||
| chr11:47032091
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.150-20297C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47032091 | ||||||
| chr11:47032349
|
T | C | 9 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0177others(6): Show | 9 | HG02647.hp1 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.150-20039T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47032349 | ||||||
| chr11:47032531
|
T | A | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.150-19857T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47032531 | ||||||
| chr11:47032559
|
A | C | 1 | a0001c0001t0001g0127 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.150-19829A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47032559 | ||||||
| chr11:47032637
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.150-19751C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47032637 | ||||||
| chr11:47032797
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.150-19591T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47032797 | ||||||
| chr11:47032816
|
A | G | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-19572A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47032816 | ||||||
| chr11:47032897
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.150-19491A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47032897 | ||||||
| chr11:47033035
|
T | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0159 | 2 | NA18955.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.150-19353T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47033035 | ||||||
| chr11:47033229
|
AT | A | 147 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(144): Show | 147 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.150-19151delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47033229 | |||||
| chr11:47033963
|
TA | T | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-18421delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47033963 | |||||
| chr11:47034049
|
T | A | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.150-18339T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47034049 | ||||||
| chr11:47034153
|
C | G | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.150-18235C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47034153 | ||||||
| chr11:47034332
|
G | A | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-18056G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47034332 | ||||||
| chr11:47034504
|
CT | C | 123 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(120): Show | 123 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.150-17869delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47034504 | |||||
| chr11:47034623
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.150-17765C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47034623 | ||||||
| chr11:47034632
|
C | G | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-17756C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47034632 | ||||||
| chr11:47034901
|
T | C | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-17487T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47034901 | ||||||
| chr11:47035209
|
A | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0170 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.150-17179A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47035209 | ||||||
| chr11:47035458
|
T | A | 126 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(123): Show | 126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.150-16930T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47035458 | ||||||
| chr11:47035639
|
C | A | 1 | a0001c0001t0001g0024 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.150-16749C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47035639 | ||||||
| chr11:47035687
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.150-16701T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47035687 | ||||||
| chr11:47036034
|
G | GAT | 11 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0018others(8): Show | 11 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.150-16333_150-1633 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | |||||
| chr11:47036034
|
G | GATATATA others(5): Show |
2 | a0001c0001t0001g0120a0001c0001t0003g0093 | 2 | HG01496.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.150-16343_150-1633 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | |||||
| chr11:47036034
|
G | GATATATA others(7): Show |
3 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0100 | 3 | HG01192.hp1 HG02004.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.150-16345_150-1633 others(18): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | |||||
| chr11:47036034
|
G | GATATATA others(9): Show |
2 | a0001c0001t0001g0083a0001c0001t0001g0135 | 2 | NA18960.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.150-16347_150-1633 others(20): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | |||||
| chr11:47036034
|
G | GATATATA others(11): Show |
4 | a0001c0001t0001g0073a0001c0001t0001g0090a0001c0001t0001g0168others(1): Show | 4 | HG01243.hp2 HG03579.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.150-16349_150-1633 others(22): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | |||||
| chr11:47036034
|
G | GATATATA others(13): Show |
2 | a0001c0001t0001g0132a0001c0001t0003g0126 | 2 | HG01081.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.150-16351_150-1633 others(24): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | |||||
| chr11:47036034
|
G | GATATATA others(15): Show |
1 | a0002c0002t0001g0087 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.150-16353_150-1633 others(26): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | |||||
| chr11:47036034
|
GAT | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG01099.hp1 HG01993.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-16333_150-1633 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | |||||
| chr11:47036034
|
GATATAT | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0094 | 2 | HG00280.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.150-16337_150-1633 others(10): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | |||||
| chr11:47036036
|
T | TAAAAGTG others(238): Show |
1 | a0001c0001t0001g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.150-16351_150-1635 others(249): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036036 | |||||
| chr11:47036036
|
T | TAAAAGTG others(226): Show |
1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.150-16351_150-1635 others(237): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036036 | |||||
| chr11:47036037
|
A | AAAAGTGG others(276): Show |
1 | a0001c0001t0001g0127 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.150-16351_150-1635 others(287): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
A | AAAAGTGG others(250): Show |
1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.150-16351_150-1635 others(261): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
A | AAAAGTGG others(255): Show |
15 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(12): Show | 15 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.150-16351_150-1635 others(266): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
A | AAAAGTGG others(224): Show |
3 | a0001c0001t0001g0175a0001c0001t0001g0184a0001c0001t0001g0187 | 3 | HG01243.hp1 HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.150-16351_150-1635 others(235): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
A | AAAAGTGG others(240): Show |
3 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.150-16351_150-1635 others(251): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
A | AAAAGTGG others(229): Show |
2 | a0001c0001t0001g0193a0005c0006t0001g0200 | 2 | HG02895.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.150-16351_150-1635 others(240): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
A | AAAAGTGG others(240): Show |
1 | a0001c0001t0002g0209 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.150-16351_150-1635 others(251): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
A | AAAAGTGG others(245): Show |
9 | a0001c0001t0002g0196a0001c0001t0002g0199a0001c0001t0002g0205others(6): Show | 9 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-16351_150-1635 others(256): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
A | AAAAGTGG others(250): Show |
12 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0201others(9): Show | 12 | HG01261.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.150-16351_150-1635 others(261): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
A | AAAAGTGG others(330): Show |
1 | a0001c0001t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.150-16351_150-1635 others(341): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
A | AAAAGTGG others(250): Show |
2 | a0001c0001t0001g0110a0001c0004t0001g0111 | 2 | HG01071.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.150-16351_150-1635 others(261): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
A | AAAAGTGG others(234): Show |
4 | a0001c0001t0001g0091a0001c0001t0001g0102a0001c0001t0001g0106others(1): Show | 4 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-16351_150-1635 others(245): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
A | AAAAGTGG others(255): Show |
17 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0108others(14): Show | 17 | HG00609.hp1 HG00621.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-16351_150-1635 others(266): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
A | AAAAGTGG others(279): Show |
1 | a0001c0001t0001g0117 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.150-16351_150-1635 others(290): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
A | AAAAGTGG others(253): Show |
1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.150-16351_150-1635 others(264): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
A | AAAAGTGG others(241): Show |
4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-16351_150-1635 others(252): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
A | AAAAGTGG others(284): Show |
1 | a0001c0005t0001g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.150-16351_150-1635 others(295): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
A | AAAAGTGG others(283): Show |
4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-16351_150-1635 others(294): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036037
|
ATATATAT others(6096): Show |
A | 47 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(44): Show | 47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-16350_150-1024 others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | ||||||
| chr11:47036043
|
A | AT | 73 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0101others(70): Show | 73 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(70): Show |
intron_variant | MODIFIER | c.150-16344dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036043 | |||||
| chr11:47036044
|
T | TA | 9 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(6): Show | 9 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-16343dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036044 | |||||
| chr11:47036048
|
TA | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0212 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.150-16339delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036048 | ||||||
| chr11:47036050
|
TA | T | 72 | a0001c0001t0001g0076a0001c0001t0001g0101a0001c0001t0001g0103others(69): Show | 72 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(69): Show |
intron_variant | MODIFIER | c.150-16337delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036050 | ||||||
| chr11:47036051
|
A | AT | 10 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(7): Show | 10 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.150-16336dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036051 | |||||
| chr11:47036058
|
A | G | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-16330A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036058 | ||||||
| chr11:47036060
|
A | ATAT | 9 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(6): Show | 9 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-16327_150-1632 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036060 | |||||
| chr11:47036062
|
A | AT | 2 | a0001c0001t0001g0081a0001c0001t0001g0212 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.150-16325dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036062 | |||||
| chr11:47036063
|
TA | T | 73 | a0001c0001t0001g0076a0001c0001t0001g0101a0001c0001t0001g0103others(70): Show | 73 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(70): Show |
intron_variant | MODIFIER | c.150-16324delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036063 | ||||||
| chr11:47036068
|
A | T | 11 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(8): Show | 11 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.150-16320A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036068 | ||||||
| chr11:47036071
|
A | AT | 9 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(6): Show | 9 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-16316dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036071 | |||||
| chr11:47036073
|
A | AT | 72 | a0001c0001t0001g0076a0001c0001t0001g0101a0001c0001t0001g0103others(69): Show | 72 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(69): Show |
intron_variant | MODIFIER | c.150-16314dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036073 | |||||
| chr11:47036074
|
T | TTATA | 2 | a0001c0001t0001g0081a0001c0001t0001g0212 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.150-16314_150-1631 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036074 | ||||||
| chr11:47036076
|
A | T | 85 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(82): Show | 85 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.150-16312A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036076 | ||||||
| chr11:47036078
|
T | A | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.150-16310T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036078 | ||||||
| chr11:47036079
|
T | A | 73 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0101others(70): Show | 73 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(70): Show |
intron_variant | MODIFIER | c.150-16309T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036079 | ||||||
| chr11:47036080
|
A | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0212 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.150-16308A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036080 | ||||||
| chr11:47036081
|
T | TA | 9 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(6): Show | 9 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-16306dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036081 | |||||
| chr11:47036084
|
A | AT | 72 | a0001c0001t0001g0076a0001c0001t0001g0101a0001c0001t0001g0103others(69): Show | 72 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(69): Show |
intron_variant | MODIFIER | c.150-16303dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036084 | |||||
| chr11:47036085
|
T | A | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.150-16303T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036085 | ||||||
| chr11:47036087
|
T | A | 1 | a0001c0001t0001g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.150-16301T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036087 | ||||||
| chr11:47036087
|
T | TA | 73 | a0001c0001t0001g0076a0001c0001t0001g0101a0001c0001t0001g0103others(70): Show | 73 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(70): Show |
intron_variant | MODIFIER | c.150-16301_150-1630 others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036087 | ||||||
| chr11:47036092
|
T | TAATATAT others(2): Show |
9 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(6): Show | 9 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-16296_150-1629 others(13): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036092 | ||||||
| chr11:47036100
|
T | A | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.150-16288T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036100 | ||||||
| chr11:47036140
|
TATATA | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0214 | 2 | HG01261.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.150-16242_150-1623 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036140 | |||||
| chr11:47036177
|
TA | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-16208delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036177 | |||||
| chr11:47036194
|
T | TATATATT others(29): Show |
1 | a0001c0001t0001g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.150-16182_150-1614 others(40): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036194 | |||||
| chr11:47036212
|
T | TTAATATA others(71): Show |
1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.150-16104_150-1610 others(82): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036212 | |||||
| chr11:47036221
|
AAT | A | 2 | a0001c0001t0001g0039a0001c0005t0001g0085 | 2 | HG00280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.150-16159_150-1615 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036221 | |||||
| chr11:47036225
|
TATATA | T | 12 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(9): Show | 12 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.150-16157_150-1615 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036225 | |||||
| chr11:47036262
|
AAT | A | 55 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(52): Show | 55 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.150-16117_150-1611 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036262 | |||||
| chr11:47036533
|
G | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.150-15855G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036533 | ||||||
| chr11:47036903
|
A | T | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-15485A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036903 | ||||||
| chr11:47036948
|
T | C | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.150-15440T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036948 | ||||||
| chr11:47037049
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.150-15339C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037049 | ||||||
| chr11:47037206
|
T | TATATCAA others(5): Show |
79 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(76): Show | 79 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.150-15182_150-1518 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037206 | ||||||
| chr11:47037392
|
A | T | 9 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(6): Show | 9 | HG01081.hp1 HG01192.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-14996A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037392 | ||||||
| chr11:47037392
|
AT | A | 72 | a0001c0001t0001g0076a0001c0001t0001g0091a0001c0001t0001g0101others(69): Show | 72 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.150-14984delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47037392 | |||||
| chr11:47037395
|
T | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(64): Show | 67 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.150-14993T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037395 | ||||||
| chr11:47037396
|
T | A | 47 | a0001c0001t0001g0076a0001c0001t0001g0117a0001c0001t0001g0129others(44): Show | 47 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.150-14992T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037396 | ||||||
| chr11:47037398
|
T | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0221others(4): Show | 7 | HG01074.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-14990T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037398 | ||||||
| chr11:47037539
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.150-14849T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037539 | ||||||
| chr11:47037597
|
C | T | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-14791C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037597 | ||||||
| chr11:47037611
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.150-14777G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037611 | ||||||
| chr11:47037662
|
G | A | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-14726G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037662 | ||||||
| chr11:47037915
|
T | C | 2 | a0002c0002t0001g0086a0002c0002t0001g0087 | 2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.150-14473T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037915 | ||||||
| chr11:47037936
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.150-14452G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037936 | ||||||
| chr11:47037972
|
G | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0062 | 2 | HG03831.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.150-14416G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037972 | ||||||
| chr11:47037986
|
C | A | 79 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(76): Show | 79 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.150-14402C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037986 | ||||||
| chr11:47038071
|
C | T | 29 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(26): Show | 29 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.150-14317C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038071 | ||||||
| chr11:47038090
|
GCCGGGCG others(43): Show |
G | 30 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(27): Show | 30 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.150-14284_150-1423 others(54): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47038090 | |||||
| chr11:47038094
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.150-14294G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038094 | ||||||
| chr11:47038106
|
A | AC | 45 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0076others(42): Show | 45 | HG01081.hp2 HG01109.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.150-14275dupC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47038106 | |||||
| chr11:47038108
|
C | T | 4 | a0001c0001t0003g0093a0001c0001t0003g0097a0001c0001t0003g0098others(1): Show | 4 | HG01081.hp1 HG01496.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-14280C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038108 | ||||||
| chr11:47038139
|
GC | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(142): Show | 145 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.150-14246delC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47038139 | |||||
| chr11:47038202
|
ACTCCTCA others(168): Show |
A | 1 | a0001c0001t0001g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.150-14157_150-1398 others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47038202 | |||||
| chr11:47038256
|
T | C | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.150-14132T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038256 | ||||||
| chr11:47038328
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.150-14060G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038328 | ||||||
| chr11:47038345
|
C | A | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-14043C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038345 | ||||||
| chr11:47038358
|
T | C | 78 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(75): Show | 78 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.150-14030T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038358 | ||||||
| chr11:47038366
|
C | T | 5 | a0001c0001t0003g0093a0001c0001t0003g0097a0001c0001t0003g0098others(2): Show | 5 | HG01081.hp1 HG01192.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-14022C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038366 | ||||||
| chr11:47038431
|
T | C | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-13957T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038431 | ||||||
| chr11:47038464
|
C | A | 1 | a0001c0001t0001g0052 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.150-13924C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038464 | ||||||
| chr11:47038489
|
C | T | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-13899C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038489 | ||||||
| chr11:47038564
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.150-13824G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038564 | ||||||
| chr11:47038641
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.150-13747C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038641 | ||||||
| chr11:47038674
|
G | C | 5 | a0001c0001t0001g0191a0001c0001t0001g0201a0001c0001t0001g0202others(2): Show | 5 | HG02109.hp1 HG02572.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-13714G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038674 | ||||||
| chr11:47038757
|
TGGGCGGA others(33): Show |
T | 1 | a0001c0001t0004g0220 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.150-13603_150-1356 others(44): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47038757 | |||||
| chr11:47038790
|
C | T | 1 | a0001c0001t0001g0021 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.150-13598C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038790 | ||||||
| chr11:47038791
|
G | A | 9 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0177others(6): Show | 9 | HG02647.hp1 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.150-13597G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038791 | ||||||
| chr11:47038797
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.150-13591C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038797 | ||||||
| chr11:47038947
|
C | G | 5 | a0001c0001t0003g0093a0001c0001t0003g0097a0001c0001t0003g0098others(2): Show | 5 | HG01081.hp1 HG01192.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-13441C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038947 | ||||||
| chr11:47039104
|
G | C | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-13284G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47039104 | ||||||
| chr11:47039202
|
G | C | 74 | a0001c0001t0001g0076a0001c0001t0001g0091a0001c0001t0001g0101others(71): Show | 74 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.150-13186G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47039202 | ||||||
| chr11:47039267
|
G | T | 1 | a0001c0005t0001g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.150-13121G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47039267 | ||||||
| chr11:47039420
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.150-12968A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47039420 | ||||||
| chr11:47039443
|
C | CAGAGGGA others(16): Show |
1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.150-12929_150-1290 others(27): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47039443 | |||||
| chr11:47039613
|
C | G | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.150-12775C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47039613 | ||||||
| chr11:47039680
|
T | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG02559.hp1 HG02723.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-12708T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47039680 | ||||||
| chr11:47040394
|
G | T | 1 | a0001c0001t0001g0070 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.150-11994G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47040394 | ||||||
| chr11:47040422
|
G | C | 2 | a0001c0001t0001g0192a0005c0006t0001g0200 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.150-11966G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47040422 | ||||||
| chr11:47040543
|
G | T | 1 | a0001c0001t0001g0077 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.150-11845G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47040543 | ||||||
| chr11:47040557
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.150-11831G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47040557 | ||||||
| chr11:47040987
|
A | G | 101 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077others(98): Show | 101 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.150-11401A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47040987 | ||||||
| chr11:47041328
|
C | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0075 | 3 | NA18973.hp2 NA18978.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.150-11060C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47041328 | ||||||
| chr11:47041380
|
G | A | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-11008G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47041380 | ||||||
| chr11:47041551
|
A | T | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.150-10837A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47041551 | ||||||
| chr11:47041603
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.150-10785C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47041603 | ||||||
| chr11:47042043
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.150-10345A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042043 | ||||||
| chr11:47042050
|
T | A | 35 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(32): Show | 35 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.150-10338T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042050 | ||||||
| chr11:47042142
|
C | A | 47 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(44): Show | 47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-10246C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042142 | ||||||
| chr11:47042147
|
A | G | 47 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(44): Show | 47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-10241A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042147 | ||||||
| chr11:47042149
|
C | A | 47 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(44): Show | 47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-10239C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042149 | ||||||
| chr11:47042151
|
A | AGT | 47 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(44): Show | 47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-10237_150-1023 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042151 | ||||||
| chr11:47042152
|
T | G | 47 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(44): Show | 47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-10236T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042152 | ||||||
| chr11:47042155
|
T | A | 47 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(44): Show | 47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-10233T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042155 | ||||||
| chr11:47042160
|
T | C | 47 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(44): Show | 47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-10228T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042160 | ||||||
| chr11:47042179
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.150-10209G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042179 | ||||||
| chr11:47042204
|
A | G | 1 | a0001c0001t0003g0093 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.150-10184A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042204 | ||||||
| chr11:47042345
|
G | GT | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0039others(4): Show | 7 | HG00280.hp1 HG01071.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-10027dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47042345 | |||||
| chr11:47042345
|
GT | G | 101 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0001t0001g0076others(98): Show | 101 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.150-10027delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47042345 | |||||
| chr11:47042351
|
T | G | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-10037T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042351 | ||||||
| chr11:47042660
|
TA | T | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-9720delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47042660 | |||||
| chr11:47042948
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.150-9440A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042948 | ||||||
| chr11:47043106
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.150-9282C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47043106 | ||||||
| chr11:47043217
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.150-9171T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47043217 | ||||||
| chr11:47043521
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.150-8867G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47043521 | ||||||
| chr11:47043630
|
A | T | 1 | a0001c0001t0001g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.150-8758A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47043630 | ||||||
| chr11:47043921
|
C | G | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-8467C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47043921 | ||||||
| chr11:47043959
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0198 | 2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.150-8429A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47043959 | ||||||
| chr11:47044144
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.150-8244G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47044144 | ||||||
| chr11:47044202
|
T | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0153 | 2 | HG00738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.150-8186T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47044202 | ||||||
| chr11:47044253
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.150-8135C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47044253 | ||||||
| chr11:47044276
|
C | G | 1 | a0002c0002t0001g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.150-8112C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47044276 | ||||||
| chr11:47044508
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.150-7880A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47044508 | ||||||
| chr11:47044789
|
G | T | 1 | a0001c0001t0001g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.150-7599G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47044789 | ||||||
| chr11:47044903
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0014 | 2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.150-7485T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47044903 | ||||||
| chr11:47045329
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.150-7059A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47045329 | ||||||
| chr11:47045355
|
CT | C | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-7030delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47045355 | |||||
| chr11:47045380
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.150-7008T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47045380 | ||||||
| chr11:47045525
|
GT | G | 8 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0116others(5): Show | 8 | HG00621.hp2 HG02080.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.150-6861delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47045525 | |||||
| chr11:47045753
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.150-6635T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47045753 | ||||||
| chr11:47045933
|
C | T | 10 | a0001c0001t0002g0196a0001c0001t0002g0199a0001c0001t0002g0205others(7): Show | 10 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.150-6455C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47045933 | ||||||
| chr11:47045960
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.150-6428T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47045960 | ||||||
| chr11:47046129
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.150-6259G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47046129 | ||||||
| chr11:47046273
|
C | A | 1 | a0001c0001t0001g0160 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.150-6115C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47046273 | ||||||
| chr11:47046626
|
C | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.150-5762C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47046626 | ||||||
| chr11:47046660
|
C | CT | 110 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0058others(107): Show | 110 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.150-5704dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47046660 | |||||
| chr11:47046660
|
C | CTT | 13 | a0001c0001t0001g0061a0001c0001t0001g0084a0001c0001t0001g0116others(10): Show | 13 | HG00438.hp1 HG00738.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.150-5705_150-5704d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47046660 | |||||
| chr11:47046660
|
CT | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(27): Show | 30 | HG00735.hp2 HG01074.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.150-5704delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47046660 | |||||
| chr11:47046660
|
CTT | C | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-5705_150-5704d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47046660 | |||||
| chr11:47046666
|
T | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0052others(7): Show | 10 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.150-5722T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47046666 | ||||||
| chr11:47046840
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.150-5548A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47046840 | ||||||
| chr11:47046904
|
C | CT | 18 | a0001c0001t0001g0062a0001c0001t0001g0073a0001c0001t0001g0083others(15): Show | 18 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.150-5470dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47046904 | |||||
| chr11:47046906
|
T | C | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.150-5482T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47046906 | ||||||
| chr11:47046927
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.150-5461G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47046927 | ||||||
| chr11:47047417
|
GA | G | 121 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(118): Show | 121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.150-4969delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47047417 | |||||
| chr11:47047421
|
C | G | 121 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(118): Show | 121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.150-4967C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47047421 | ||||||
| chr11:47047741
|
G | T | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.150-4647G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47047741 | ||||||
| chr11:47047983
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.150-4405G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47047983 | ||||||
| chr11:47048197
|
G | A | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-4191G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47048197 | ||||||
| chr11:47048527
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.150-3861A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47048527 | ||||||
| chr11:47048874
|
G | C | 47 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(44): Show | 47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-3514G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47048874 | ||||||
| chr11:47049364
|
C | T | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-3024C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47049364 | ||||||
| chr11:47049494
|
T | G | 1 | a0001c0001t0001g0108 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.150-2894T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47049494 | ||||||
| chr11:47049546
|
G | C | 1 | a0001c0001t0001g0068 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.150-2842G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47049546 | ||||||
| chr11:47049607
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.150-2781C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47049607 | ||||||
| chr11:47049962
|
C | T | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-2426C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47049962 | ||||||
| chr11:47050164
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.150-2224T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47050164 | ||||||
| chr11:47050346
|
C | T | 156 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(153): Show | 156 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(153): Show |
intron_variant | MODIFIER | c.150-2042C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47050346 | ||||||
| chr11:47050349
|
G | A | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-2039G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47050349 | ||||||
| chr11:47050498
|
G | T | 1 | a0001c0001t0001g0021 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.150-1890G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47050498 | ||||||
| chr11:47050791
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.150-1597G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47050791 | ||||||
| chr11:47051104
|
T | C | 121 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(118): Show | 121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.150-1284T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47051104 | ||||||
| chr11:47051162
|
T | C | 16 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(13): Show | 16 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.150-1226T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47051162 | ||||||
| chr11:47051163
|
C | G | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.150-1225C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47051163 | ||||||
| chr11:47051254
|
G | T | 121 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(118): Show | 121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.150-1134G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47051254 | ||||||
| chr11:47051318
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.150-1070G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47051318 | ||||||
| chr11:47051611
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.150-777T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47051611 | ||||||
| chr11:47051691
|
C | CT | 11 | a0001c0001t0001g0030a0001c0001t0001g0062a0001c0001t0001g0101others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.150-679dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47051691 | |||||
| chr11:47052275
|
G | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0066 | 2 | HG03017.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.150-113G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47052275 | ||||||
| chr11:47052539
|
T | TTTCC | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+44_280+47dupCC others(2): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47052539 | |||||
| chr11:47052583
|
CTCTCTCT others(9): Show |
C | 1 | a0001c0004t0001g0111 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.280+79_280+94delCT others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47052583 | |||||
| chr11:47052928
|
T | C | 148 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.280+410T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47052928 | ||||||
| chr11:47053245
|
T | A | 3 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.280+727T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47053245 | ||||||
| chr11:47053548
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.280+1030G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47053548 | ||||||
| chr11:47053619
|
C | CA | 9 | a0001c0001t0001g0022a0001c0001t0001g0110a0001c0001t0001g0158others(6): Show | 9 | HG01071.hp1 HG01515.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.280+1116dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47053619 | |||||
| chr11:47053771
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.280+1253G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47053771 | ||||||
| chr11:47053778
|
C | CA | 121 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(118): Show | 121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.280+1267dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47053778 | |||||
| chr11:47053945
|
AAAAC | A | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+1443_280+1446d others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47053945 | |||||
| chr11:47054032
|
G | A | 1 | a0002c0002t0001g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.280+1514G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47054032 | ||||||
| chr11:47054208
|
G | T | 1 | a0001c0001t0001g0145 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.280+1690G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47054208 | ||||||
| chr11:47054310
|
C | CA | 38 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0034others(35): Show | 38 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.280+1815dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47054310 | |||||
| chr11:47054310
|
C | CAA | 11 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0175others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.280+1814_280+1815d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47054310 | |||||
| chr11:47054310
|
C | CAAA | 5 | a0001c0001t0001g0174a0001c0001t0001g0177a0001c0001t0001g0180others(2): Show | 5 | HG02559.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+1813_280+1815d others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47054310 | |||||
| chr11:47054593
|
A | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280+2075A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47054593 | ||||||
| chr11:47054836
|
A | G | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+2318A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47054836 | ||||||
| chr11:47054928
|
A | AT | 12 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0022others(9): Show | 12 | HG00642.hp2 HG00673.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.280+2439dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47054928 | |||||
| chr11:47054928
|
A | ATT | 5 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0036others(2): Show | 5 | NA18983.hp1 NA18992.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+2438_280+2439d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47054928 | |||||
| chr11:47054928
|
AT | A | 30 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(27): Show | 30 | HG00735.hp1 HG01074.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.280+2439delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47054928 | |||||
| chr11:47054928
|
ATT | A | 52 | a0001c0001t0001g0011a0001c0001t0001g0073a0001c0001t0001g0082others(49): Show | 52 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.280+2438_280+2439d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47054928 | |||||
| chr11:47054928
|
ATTT | A | 78 | a0001c0001t0001g0076a0001c0001t0001g0090a0001c0001t0001g0091others(75): Show | 78 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.280+2437_280+2439d others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47054928 | |||||
| chr11:47055003
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.280+2485C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47055003 | ||||||
| chr11:47055420
|
C | G | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.280+2902C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47055420 | ||||||
| chr11:47055481
|
A | G | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+2963A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47055481 | ||||||
| chr11:47055533
|
G | A | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+3015G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47055533 | ||||||
| chr11:47055593
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.280+3075A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47055593 | ||||||
| chr11:47055695
|
T | A | 148 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.280+3177T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47055695 | ||||||
| chr11:47056148
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.280+3630A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47056148 | ||||||
| chr11:47056286
|
C | T | 148 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.280+3768C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47056286 | ||||||
| chr11:47056407
|
T | C | 3 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0134 | 3 | NA18949.hp1 NA18977.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.280+3889T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47056407 | ||||||
| chr11:47056436
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0186 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.280+3918G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47056436 | ||||||
| chr11:47057318
|
A | T | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+4800A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47057318 | ||||||
| chr11:47057408
|
A | G | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+4890A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47057408 | ||||||
| chr11:47057680
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.280+5162G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47057680 | ||||||
| chr11:47057684
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0072 | 2 | NA18964.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.280+5166T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47057684 | ||||||
| chr11:47057876
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.280+5358C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47057876 | ||||||
| chr11:47057925
|
C | T | 4 | a0001c0001t0001g0175a0001c0001t0001g0184a0001c0001t0001g0187others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+5407C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47057925 | ||||||
| chr11:47058096
|
G | A | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+5578G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47058096 | ||||||
| chr11:47058143
|
G | C | 1 | a0001c0001t0001g0090 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.280+5625G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47058143 | ||||||
| chr11:47058636
|
T | C | 9 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0177others(6): Show | 9 | HG02647.hp1 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.280+6118T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47058636 | ||||||
| chr11:47058800
|
C | T | 1 | a0003c0003t0001g0113 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280+6282C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47058800 | ||||||
| chr11:47058831
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.280+6313G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47058831 | ||||||
| chr11:47059199
|
T | G | 1 | a0001c0001t0001g0188 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.280+6681T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47059199 | ||||||
| chr11:47059559
|
G | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0116others(4): Show | 7 | HG00621.hp2 HG02080.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+7041G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47059559 | ||||||
| chr11:47059579
|
G | T | 1 | a0001c0001t0003g0126 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.280+7061G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47059579 | ||||||
| chr11:47059741
|
T | C | 1 | a0003c0003t0001g0113 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280+7223T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47059741 | ||||||
| chr11:47059919
|
C | T | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+7401C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47059919 | ||||||
| chr11:47059963
|
G | T | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+7445G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47059963 | ||||||
| chr11:47060134
|
C | CA | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(220): Show | 223 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.280+7616_280+7617i others(3): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47060134 | ||||||
| chr11:47060181
|
C | T | 126 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(123): Show | 126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.280+7663C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47060181 | ||||||
| chr11:47060258
|
C | CT | 20 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(17): Show | 20 | HG00597.hp1 HG00642.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.280+7760dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47060258 | |||||
| chr11:47060258
|
CT | C | 124 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0081others(121): Show | 124 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.280+7760delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47060258 | |||||
| chr11:47060263
|
T | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(7): Show | 10 | HG00735.hp2 HG01074.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+7745T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47060263 | ||||||
| chr11:47060484
|
C | T | 2 | a0002c0002t0001g0086a0002c0002t0001g0087 | 2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.280+7966C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47060484 | ||||||
| chr11:47060571
|
C | A | 148 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.280+8053C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47060571 | ||||||
| chr11:47060704
|
G | T | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+8186G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47060704 | ||||||
| chr11:47060873
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.280+8355G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47060873 | ||||||
| chr11:47060913
|
C | T | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+8395C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47060913 | ||||||
| chr11:47061280
|
A | G | 5 | a0001c0001t0001g0124a0001c0001t0001g0128a0001c0001t0001g0149others(2): Show | 5 | HG00733.hp2 HG00735.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+8762A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47061280 | ||||||
| chr11:47061307
|
T | C | 76 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(73): Show | 76 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.280+8789T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47061307 | ||||||
| chr11:47061831
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280+9313T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47061831 | ||||||
| chr11:47062510
|
G | C | 127 | a0001c0001t0001g0069a0001c0001t0001g0076a0001c0001t0001g0077others(124): Show | 127 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.280+9992G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47062510 | ||||||
| chr11:47062669
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.280+10151C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47062669 | ||||||
| chr11:47062813
|
C | T | 1 | a0001c0005t0001g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+10295C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47062813 | ||||||
| chr11:47062835
|
C | A | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+10317C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47062835 | ||||||
| chr11:47063320
|
A | T | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+10802A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063320 | ||||||
| chr11:47063360
|
T | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0103 | 2 | NA18973.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.280+10842T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063360 | ||||||
| chr11:47063375
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.280+10857G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063375 | ||||||
| chr11:47063561
|
A | G | 1 | a0003c0003t0001g0113 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280+11043A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063561 | ||||||
| chr11:47063626
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280+11108T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063626 | ||||||
| chr11:47063638
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0061 | 2 | HG01192.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.280+11120G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063638 | ||||||
| chr11:47063758
|
G | A | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+11240G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063758 | ||||||
| chr11:47063806
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.280+11288T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063806 | ||||||
| chr11:47063916
|
A | C | 1 | a0001c0001t0001g0077 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.280+11398A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063916 | ||||||
| chr11:47064259
|
T | TGTAG | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+11744_280+1174 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47064259 | |||||
| chr11:47064261
|
T | C | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+11743T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47064261 | ||||||
| chr11:47064872
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.280+12354G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47064872 | ||||||
| chr11:47065117
|
G | A | 5 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+12599G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47065117 | ||||||
| chr11:47065315
|
A | AT | 18 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(15): Show | 18 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.280+12807dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065315 | |||||
| chr11:47065412
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.280+12894C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47065412 | ||||||
| chr11:47065577
|
C | G | 123 | a0001c0001t0001g0044a0001c0001t0001g0050a0001c0001t0001g0076others(120): Show | 123 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.280+13059C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47065577 | ||||||
| chr11:47065616
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.280+13098C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47065616 | ||||||
| chr11:47065754
|
A | T | 10 | a0001c0001t0002g0196a0001c0001t0002g0199a0001c0001t0002g0205others(7): Show | 10 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.280+13236A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47065754 | ||||||
| chr11:47065757
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.280+13239T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47065757 | ||||||
| chr11:47065789
|
G | T | 49 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(46): Show | 49 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.280+13271G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47065789 | ||||||
| chr11:47065898
|
C | A | 1 | a0001c0001t0001g0125 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.280+13380C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47065898 | ||||||
| chr11:47065977
|
T | TTG | 4 | a0001c0001t0001g0039a0001c0001t0001g0056a0001c0001t0001g0059others(1): Show | 4 | HG00280.hp1 HG01071.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+13483_280+1348 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | |||||
| chr11:47065977
|
T | TTGTG | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+13481_280+1348 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | |||||
| chr11:47065977
|
T | TTGTGTG | 16 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(13): Show | 16 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.280+13479_280+1348 others(10): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | |||||
| chr11:47065977
|
T | TTGTGTGT others(1): Show |
6 | a0001c0001t0001g0073a0001c0001t0001g0081a0001c0001t0001g0083others(3): Show | 6 | HG02451.hp1 HG03654.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.280+13477_280+1348 others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | |||||
| chr11:47065977
|
T | TTGTGTGT others(3): Show |
10 | a0001c0001t0001g0077a0001c0001t0001g0095a0001c0001t0001g0116others(7): Show | 10 | HG00597.hp2 HG00609.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+13475_280+1348 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | |||||
| chr11:47065977
|
T | TTGTGTGT others(5): Show |
33 | a0001c0001t0001g0112a0001c0001t0001g0119a0001c0001t0001g0121others(30): Show | 33 | HG00280.hp2 HG00733.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.280+13473_280+1348 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | |||||
| chr11:47065977
|
T | TTGTGTGT others(7): Show |
57 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(54): Show | 57 | HG00438.hp1 HG00621.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.280+13471_280+1348 others(18): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | |||||
| chr11:47065977
|
T | TTGTGTGT others(9): Show |
8 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0174others(5): Show | 8 | HG00673.hp1 HG00741.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.280+13469_280+1348 others(20): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | |||||
| chr11:47065977
|
T | TTGTGTGT others(11): Show |
11 | a0001c0001t0001g0172a0001c0001t0001g0175a0001c0001t0001g0176others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.280+13467_280+1348 others(22): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | |||||
| chr11:47065977
|
T | TTGTGTGT others(13): Show |
2 | a0001c0001t0001g0154a0001c0001t0001g0194 | 2 | HG03579.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.280+13465_280+1348 others(24): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | |||||
| chr11:47065977
|
T | TTGTGTGT others(15): Show |
1 | a0001c0001t0001g0182 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.280+13463_280+1348 others(26): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | |||||
| chr11:47066093
|
G | GGTT | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+13575_280+1357 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066093 | ||||||
| chr11:47066099
|
T | TTTG | 127 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0078others(124): Show | 127 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.280+13583_280+1358 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47066099 | |||||
| chr11:47066102
|
T | G | 20 | a0001c0001t0001g0076a0001c0001t0001g0108a0001c0001t0001g0145others(17): Show | 20 | HG01243.hp1 HG01884.hp1 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.280+13584T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066102 | ||||||
| chr11:47066102
|
T | TG | 3 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0051 | 3 | HG01361.hp2 HG01975.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.280+13584_280+1358 others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066102 | ||||||
| chr11:47066109
|
T | G | 4 | a0001c0001t0001g0104a0001c0001t0001g0146a0001c0001t0001g0156others(1): Show | 4 | HG00735.hp1 HG01496.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+13591T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066109 | ||||||
| chr11:47066112
|
T | G | 128 | a0001c0001t0001g0010a0001c0001t0001g0073a0001c0001t0001g0077others(125): Show | 128 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.280+13594T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066112 | ||||||
| chr11:47066115
|
T | G | 148 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.280+13597T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066115 | ||||||
| chr11:47066115
|
T | TG | 41 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0017others(38): Show | 41 | HG00597.hp1 HG00642.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.280+13597_280+1359 others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066115 | ||||||
| chr11:47066115
|
T | TGTTG | 20 | a0001c0001t0001g0076a0001c0001t0001g0108a0001c0001t0001g0145others(17): Show | 20 | HG01243.hp1 HG01884.hp1 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.280+13597_280+1359 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066115 | ||||||
| chr11:47066115
|
T | TTG | 11 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0047others(8): Show | 11 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(8): Show |
intron_variant | MODIFIER | c.280+13598_280+1359 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47066115 | |||||
| chr11:47066610
|
A | G | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+14092A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066610 | ||||||
| chr11:47066747
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.280+14229G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066747 | ||||||
| chr11:47066752
|
T | C | 126 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(123): Show | 126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.280+14234T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066752 | ||||||
| chr11:47066819
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.280+14301G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066819 | ||||||
| chr11:47067199
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.280+14681G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47067199 | ||||||
| chr11:47067330
|
A | G | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+14812A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47067330 | ||||||
| chr11:47067416
|
C | T | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+14898C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47067416 | ||||||
| chr11:47067830
|
G | A | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.280+15312G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47067830 | ||||||
| chr11:47067930
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.280+15412G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47067930 | ||||||
| chr11:47068011
|
G | A | 1 | a0001c0001t0001g0022 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.280+15493G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47068011 | ||||||
| chr11:47068100
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.280+15582C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47068100 | ||||||
| chr11:47068139
|
C | T | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+15621C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47068139 | ||||||
| chr11:47068361
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.280+15843G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47068361 | ||||||
| chr11:47068783
|
A | G | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+16265A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47068783 | ||||||
| chr11:47068867
|
A | C | 10 | a0001c0001t0001g0191a0001c0001t0001g0201a0001c0001t0001g0202others(7): Show | 10 | HG01261.hp1 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+16349A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47068867 | ||||||
| chr11:47069291
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.280+16773C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47069291 | ||||||
| chr11:47069716
|
A | T | 13 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(10): Show | 13 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.280+17198A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47069716 | ||||||
| chr11:47069719
|
T | A | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+17201T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47069719 | ||||||
| chr11:47070004
|
C | T | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+17486C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47070004 | ||||||
| chr11:47070020
|
C | T | 126 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(123): Show | 126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.280+17502C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47070020 | ||||||
| chr11:47070387
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.280+17869C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47070387 | ||||||
| chr11:47070484
|
A | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.280+17966A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47070484 | ||||||
| chr11:47071131
|
C | T | 18 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(15): Show | 18 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.280+18613C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47071131 | ||||||
| chr11:47071152
|
G | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.280+18634G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47071152 | ||||||
| chr11:47071533
|
T | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(72): Show | 75 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.280+19015T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47071533 | ||||||
| chr11:47071666
|
C | CA | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+19150dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47071666 | |||||
| chr11:47071914
|
C | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(72): Show | 75 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.280+19396C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47071914 | ||||||
| chr11:47072012
|
C | T | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+19494C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47072012 | ||||||
| chr11:47072089
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.280+19571T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47072089 | ||||||
| chr11:47072717
|
C | CTTATG | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 97 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.280+20203_280+2020 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47072717 | |||||
| chr11:47072742
|
C | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0170 | 2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.280+20224C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47072742 | ||||||
| chr11:47072925
|
T | C | 1 | a0001c0001t0002g0205 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.280+20407T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47072925 | ||||||
| chr11:47072935
|
A | C | 1 | a0001c0001t0001g0148 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.280+20417A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47072935 | ||||||
| chr11:47072959
|
A | G | 1 | a0001c0005t0001g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+20441A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47072959 | ||||||
| chr11:47072995
|
G | A | 15 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(12): Show | 15 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.280+20477G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47072995 | ||||||
| chr11:47073505
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.280+20987G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47073505 | ||||||
| chr11:47073943
|
G | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.280+21425G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47073943 | ||||||
| chr11:47073960
|
G | C | 75 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(72): Show | 75 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.280+21442G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47073960 | ||||||
| chr11:47074501
|
GAAAAA | G | 17 | a0001c0001t0001g0091a0001c0001t0001g0102a0001c0001t0001g0106others(14): Show | 17 | HG00609.hp1 HG00738.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.280+21999_280+2200 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47074501 | |||||
| chr11:47074501
|
GAAAAAA | G | 54 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(51): Show | 54 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.280+21998_280+2200 others(10): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47074501 | |||||
| chr11:47074501
|
GAAAAAAA others(3): Show |
G | 23 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(20): Show | 23 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.280+21994_280+2200 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47074501 | |||||
| chr11:47074512
|
A | C | 1 | a0001c0001t0002g0217 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.280+21994A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074512 | ||||||
| chr11:47074514
|
A | G | 1 | a0001c0001t0002g0217 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.280+21996A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074514 | ||||||
| chr11:47074515
|
A | AC | 21 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0173others(18): Show | 21 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.280+21997_280+2199 others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074515 | ||||||
| chr11:47074515
|
A | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(95): Show | 98 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.280+21997A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074515 | ||||||
| chr11:47074516
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.280+21998A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074516 | ||||||
| chr11:47074518
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.280+22000A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074518 | ||||||
| chr11:47074855
|
C | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+22337C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074855 | ||||||
| chr11:47074870
|
G | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+22352G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074870 | ||||||
| chr11:47074879
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.280+22361A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074879 | ||||||
| chr11:47074885
|
T | A | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.280+22367T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074885 | ||||||
| chr11:47074982
|
G | C | 1 | a0001c0001t0001g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.280+22464G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074982 | ||||||
| chr11:47075292
|
AC | A | 101 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(98): Show | 101 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.280+22777delC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47075292 | |||||
| chr11:47075329
|
G | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+22811G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075329 | ||||||
| chr11:47075430
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+22912G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075430 | ||||||
| chr11:47075508
|
A | G | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+22990A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075508 | ||||||
| chr11:47075509
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.280+22991T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075509 | ||||||
| chr11:47075603
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.280+23085G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075603 | ||||||
| chr11:47075713
|
G | A | 4 | a0001c0001t0001g0175a0001c0001t0001g0184a0001c0001t0001g0187others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+23195G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075713 | ||||||
| chr11:47075733
|
G | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.280+23215G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075733 | ||||||
| chr11:47075747
|
C | T | 18 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(15): Show | 18 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.280+23229C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075747 | ||||||
| chr11:47075813
|
G | T | 101 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(98): Show | 101 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.280+23295G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075813 | ||||||
| chr11:47075926
|
C | CA | 24 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0033others(21): Show | 24 | HG00438.hp2 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.280+23434dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47075926 | |||||
| chr11:47075926
|
CA | C | 66 | a0001c0001t0001g0066a0001c0001t0001g0076a0001c0001t0001g0082others(63): Show | 66 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.280+23434delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47075926 | |||||
| chr11:47076374
|
C | G | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+23856C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47076374 | ||||||
| chr11:47076602
|
A | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0168 | 2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.280+24084A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47076602 | ||||||
| chr11:47076726
|
C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(7): Show | 10 | HG00642.hp2 HG00733.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+24208C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47076726 | ||||||
| chr11:47076894
|
A | C | 120 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(117): Show | 120 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.280+24376A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47076894 | ||||||
| chr11:47076918
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.280+24400G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47076918 | ||||||
| chr11:47076963
|
GA | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 215 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.280+24460delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47076963 | |||||
| chr11:47077196
|
GT | G | 103 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(100): Show | 103 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.280+24693delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47077196 | |||||
| chr11:47077269
|
G | T | 1 | a0001c0001t0002g0217 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.280+24751G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47077269 | ||||||
| chr11:47077333
|
G | C | 5 | a0001c0001t0003g0093a0001c0001t0003g0097a0001c0001t0003g0098others(2): Show | 5 | HG01081.hp1 HG01192.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+24815G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47077333 | ||||||
| chr11:47077384
|
A | G | 2 | a0001c0001t0002g0205a0001c0001t0002g0218 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.280+24866A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47077384 | ||||||
| chr11:47077574
|
A | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(66): Show | 69 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.280+25056A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47077574 | ||||||
| chr11:47077616
|
T | G | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+25098T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47077616 | ||||||
| chr11:47078191
|
A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0178 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.280+25673A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47078191 | ||||||
| chr11:47078208
|
T | C | 2 | a0001c0001t0001g0140a0001c0001t0001g0161 | 2 | HG00597.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.280+25690T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47078208 | ||||||
| chr11:47078218
|
T | A | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280+25700T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47078218 | ||||||
| chr11:47078298
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.280+25780G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47078298 | ||||||
| chr11:47078316
|
C | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(7): Show | 10 | HG00735.hp2 HG01074.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+25798C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47078316 | ||||||
| chr11:47078595
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.280+26077T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47078595 | ||||||
| chr11:47079245
|
G | T | 76 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(73): Show | 76 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.280+26727G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47079245 | ||||||
| chr11:47079948
|
T | G | 1 | a0001c0001t0001g0161 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.280+27430T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47079948 | ||||||
| chr11:47080363
|
G | T | 1 | a0001c0001t0002g0217 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.280+27845G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47080363 | ||||||
| chr11:47080523
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.280+28005A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47080523 | ||||||
| chr11:47080632
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0170others(1): Show | 4 | HG01071.hp1 HG01515.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+28114G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47080632 | ||||||
| chr11:47080896
|
C | G | 1 | a0001c0001t0001g0160 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.280+28378C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47080896 | ||||||
| chr11:47081008
|
CA | C | 20 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0030others(17): Show | 20 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.280+28506delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47081008 | |||||
| chr11:47081103
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.280+28585G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47081103 | ||||||
| chr11:47081935
|
C | CT | 11 | a0001c0001t0001g0056a0001c0001t0001g0106a0001c0001t0001g0112others(8): Show | 11 | HG00738.hp2 HG01243.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.280+29435dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47081935 | |||||
| chr11:47081935
|
CT | C | 9 | a0001c0001t0002g0196a0001c0001t0002g0199a0001c0001t0002g0205others(6): Show | 9 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.280+29435delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47081935 | |||||
| chr11:47082142
|
C | A | 1 | a0001c0001t0001g0007 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.280+29624C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47082142 | ||||||
| chr11:47082149
|
C | CA | 33 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(30): Show | 33 | HG00673.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.280+29649dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47082149 | |||||
| chr11:47082149
|
C | CAA | 44 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(41): Show | 44 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.280+29648_280+2964 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47082149 | |||||
| chr11:47082149
|
C | CAAA | 14 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0045others(11): Show | 14 | HG00438.hp2 HG01192.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.280+29647_280+2964 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47082149 | |||||
| chr11:47082257
|
A | T | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+29739A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47082257 | ||||||
| chr11:47082326
|
C | T | 16 | a0001c0001t0001g0091a0001c0001t0001g0102a0001c0001t0001g0106others(13): Show | 16 | HG00609.hp1 HG00738.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.280+29808C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47082326 | ||||||
| chr11:47082490
|
C | CAG | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.280+29975_280+2997 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47082490 | |||||
| chr11:47082848
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.280+30330T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47082848 | ||||||
| chr11:47083390
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.280+30872C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47083390 | ||||||
| chr11:47083610
|
T | TA | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+31093dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47083610 | |||||
| chr11:47083701
|
G | A | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+31183G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47083701 | ||||||
| chr11:47083769
|
G | C | 1 | a0001c0001t0001g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.280+31251G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47083769 | ||||||
| chr11:47083906
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0052 | 2 | HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.280+31388A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47083906 | ||||||
| chr11:47084180
|
C | G | 1 | a0001c0001t0001g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.280+31662C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47084180 | ||||||
| chr11:47084312
|
A | G | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+31794A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47084312 | ||||||
| chr11:47084379
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.280+31861T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47084379 | ||||||
| chr11:47084763
|
G | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0116others(4): Show | 7 | HG00621.hp2 HG02080.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+32245G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47084763 | ||||||
| chr11:47084979
|
G | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+32461G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47084979 | ||||||
| chr11:47085129
|
G | A | 1 | a0001c0001t0003g0097 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.280+32611G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47085129 | ||||||
| chr11:47085443
|
G | A | 17 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+32925G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47085443 | ||||||
| chr11:47085458
|
T | A | 5 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+32940T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47085458 | ||||||
| chr11:47085718
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0052others(2): Show | 5 | HG01074.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+33200C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47085718 | ||||||
| chr11:47085863
|
G | C | 1 | a0003c0003t0001g0113 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280+33345G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47085863 | ||||||
| chr11:47085870
|
T | A | 3 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.280+33352T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47085870 | ||||||
| chr11:47085985
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.280+33467G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47085985 | ||||||
| chr11:47086113
|
G | T | 1 | a0001c0001t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.280+33595G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086113 | ||||||
| chr11:47086232
|
T | TA | 49 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(46): Show | 49 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.280+33714_280+3371 others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086232 | ||||||
| chr11:47086232
|
TCCAAAAA others(1): Show |
T | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+33715_280+3372 others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086232 | ||||||
| chr11:47086233
|
C | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(160): Show | 163 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.280+33715C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086233 | ||||||
| chr11:47086234
|
C | A | 49 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(46): Show | 49 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.280+33716C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086234 | ||||||
| chr11:47086234
|
C | CAA | 34 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(31): Show | 34 | HG00597.hp1 HG00642.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.280+33738_280+3373 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47086234 | |||||
| chr11:47086234
|
C | CAAA | 39 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(36): Show | 39 | HG00738.hp1 HG01109.hp2 HG01261.hp1 others(36): Show |
intron_variant | MODIFIER | c.280+33737_280+3373 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47086234 | |||||
| chr11:47086234
|
C | CAAAA | 76 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0084others(73): Show | 76 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.280+33736_280+3373 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47086234 | |||||
| chr11:47086234
|
C | CAAAAA | 12 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0103others(9): Show | 12 | HG00280.hp2 HG00597.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.280+33735_280+3373 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47086234 | |||||
| chr11:47086237
|
A | C | 2 | a0001c0001t0001g0174a0001c0001t0001g0180 | 2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.280+33719A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086237 | ||||||
| chr11:47086238
|
A | C | 1 | a0001c0001t0001g0068 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.280+33720A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086238 | ||||||
| chr11:47086239
|
A | C | 2 | a0001c0001t0001g0179a0001c0001t0001g0186 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.280+33721A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086239 | ||||||
| chr11:47086240
|
A | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0147 | 2 | HG02293.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.280+33722A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086240 | ||||||
| chr11:47086242
|
A | C | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+33724A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086242 | ||||||
| chr11:47086340
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.280+33822C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086340 | ||||||
| chr11:47086618
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.280+34100A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086618 | ||||||
| chr11:47086650
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.280+34132T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086650 | ||||||
| chr11:47087259
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.280+34741A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087259 | ||||||
| chr11:47087261
|
G | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.280+34743G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087261 | ||||||
| chr11:47087304
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.280+34786T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087304 | ||||||
| chr11:47087509
|
A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 74 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.280+34991A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087509 | ||||||
| chr11:47087706
|
A | T | 1 | a0001c0001t0001g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.280+35188A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087706 | ||||||
| chr11:47087717
|
A | ATG | 5 | a0001c0001t0001g0096a0001c0001t0001g0174a0001c0001t0001g0180others(2): Show | 5 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+35218_280+3521 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47087717 | |||||
| chr11:47087780
|
C | A | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+35262C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087780 | ||||||
| chr11:47087792
|
A | G | 8 | a0001c0001t0001g0191a0001c0001t0001g0201a0001c0001t0001g0202others(5): Show | 8 | HG02109.hp1 HG02572.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.280+35274A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087792 | ||||||
| chr11:47087912
|
T | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 74 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.280+35394T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087912 | ||||||
| chr11:47087963
|
G | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 97 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.280+35445G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087963 | ||||||
| chr11:47088257
|
G | C | 1 | a0001c0001t0001g0157 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.280+35739G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47088257 | ||||||
| chr11:47088273
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.280+35755A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47088273 | ||||||
| chr11:47088628
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.280+36110C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47088628 | ||||||
| chr11:47088798
|
G | A | 121 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(118): Show | 121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.280+36280G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47088798 | ||||||
| chr11:47088995
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.280+36477T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47088995 | ||||||
| chr11:47089041
|
C | T | 18 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(15): Show | 18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.280+36523C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47089041 | ||||||
| chr11:47089058
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.280+36540A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47089058 | ||||||
| chr11:47089096
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280+36578G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47089096 | ||||||
| chr11:47089101
|
A | C | 121 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(118): Show | 121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.280+36583A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47089101 | ||||||
| chr11:47089435
|
A | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.280+36917A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47089435 | ||||||
| chr11:47090067
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.280+37549T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47090067 | ||||||
| chr11:47090255
|
G | T | 18 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(15): Show | 18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.280+37737G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47090255 | ||||||
| chr11:47090310
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.280+37792T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47090310 | ||||||
| chr11:47090467
|
GA | G | 10 | a0001c0001t0002g0196a0001c0001t0002g0199a0001c0001t0002g0205others(7): Show | 10 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.280+37958delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47090467 | |||||
| chr11:47090843
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.280+38325T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47090843 | ||||||
| chr11:47090901
|
C | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.280+38383C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47090901 | ||||||
| chr11:47091046
|
CA | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(132): Show | 135 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.280+38547delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47091046 | |||||
| chr11:47091046
|
CAA | C | 80 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0068others(77): Show | 80 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.280+38546_280+3854 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47091046 | |||||
| chr11:47091113
|
T | C | 1 | a0001c0001t0003g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.280+38595T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47091113 | ||||||
| chr11:47091336
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.280+38818T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47091336 | ||||||
| chr11:47091373
|
C | CA | 14 | a0001c0001t0001g0132a0001c0001t0001g0192a0001c0001t0001g0211others(11): Show | 14 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.280+38869dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47091373 | |||||
| chr11:47091522
|
G | T | 1 | a0001c0005t0001g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+39004G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47091522 | ||||||
| chr11:47091752
|
C | T | 18 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(15): Show | 18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.280+39234C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47091752 | ||||||
| chr11:47092455
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.280+39937T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47092455 | ||||||
| chr11:47092523
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.280+40005C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47092523 | ||||||
| chr11:47092577
|
A | T | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+40059A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47092577 | ||||||
| chr11:47092788
|
A | G | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+40270A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47092788 | ||||||
| chr11:47092937
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.280+40419C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47092937 | ||||||
| chr11:47093232
|
G | T | 1 | a0001c0001t0001g0161 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.280+40714G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47093232 | ||||||
| chr11:47093273
|
G | A | 13 | a0001c0001t0001g0089a0001c0001t0001g0096a0001c0001t0001g0104others(10): Show | 13 | HG00597.hp2 HG00673.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.280+40755G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47093273 | ||||||
| chr11:47093487
|
C | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.280+40969C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47093487 | ||||||
| chr11:47093720
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280+41202G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47093720 | ||||||
| chr11:47093906
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.280+41388C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47093906 | ||||||
| chr11:47094002
|
G | C | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.280+41484G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094002 | ||||||
| chr11:47094168
|
G | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 74 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.280+41650G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094168 | ||||||
| chr11:47094206
|
C | T | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.280+41688C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094206 | ||||||
| chr11:47094217
|
A | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(2): Show | 5 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+41699A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094217 | ||||||
| chr11:47094416
|
C | T | 18 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(15): Show | 18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.280+41898C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094416 | ||||||
| chr11:47094422
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.280+41904T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094422 | ||||||
| chr11:47094464
|
T | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.280+41946T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094464 | ||||||
| chr11:47094480
|
C | CAG | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(69): Show | 72 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.280+41984_280+4198 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47094480 | |||||
| chr11:47094482
|
G | C | 102 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(99): Show | 102 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.280+41964G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094482 | ||||||
| chr11:47094545
|
C | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.280+42027C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094545 | ||||||
| chr11:47094698
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0186 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.280+42180G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094698 | ||||||
| chr11:47094950
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.280+42432A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094950 | ||||||
| chr11:47095272
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 74 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.281-42373T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47095272 | ||||||
| chr11:47095581
|
A | C | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.281-42064A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47095581 | ||||||
| chr11:47095718
|
G | A | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0219 | 3 | HG03516.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.281-41927G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47095718 | ||||||
| chr11:47095856
|
A | AT | 6 | a0001c0001t0002g0199a0001c0001t0002g0205a0001c0001t0002g0206others(3): Show | 6 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.281-41781dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47095856 | |||||
| chr11:47096157
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0071others(1): Show | 4 | NA18951.hp1 NA18971.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-41488T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47096157 | ||||||
| chr11:47096576
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.281-41069C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47096576 | ||||||
| chr11:47096811
|
G | GA | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(93): Show | 96 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.281-40818dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47096811 | |||||
| chr11:47097065
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.281-40580C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097065 | ||||||
| chr11:47097067
|
C | G | 1 | a0002c0002t0001g0087 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.281-40578C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097067 | ||||||
| chr11:47097071
|
CGGCCAGC others(42): Show |
C | 1 | a0001c0001t0001g0055 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.281-40545_281-4049 others(53): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097071 | |||||
| chr11:47097120
|
T | C | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(53): Show | 56 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.281-40525T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097120 | ||||||
| chr11:47097121
|
G | A | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(53): Show | 56 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.281-40524G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097121 | ||||||
| chr11:47097154
|
T | G | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(53): Show | 56 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.281-40491T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097154 | ||||||
| chr11:47097162
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.281-40483C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097162 | ||||||
| chr11:47097211
|
A | G | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 58 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.281-40434A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097211 | ||||||
| chr11:47097243
|
TGCCCGGC others(348): Show |
T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-40360_281-4000 others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097243 | |||||
| chr11:47097248
|
GGCCAGCC others(42): Show |
G | 5 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0052others(2): Show | 5 | HG01074.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-40355_281-4030 others(53): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097248 | |||||
| chr11:47097285
|
A | G | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(53): Show | 56 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.281-40360A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097285 | ||||||
| chr11:47097290
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.281-40355C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097290 | ||||||
| chr11:47097292
|
CGCCCAGC others(120): Show |
C | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(51): Show | 54 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.281-40348_281-4022 others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097292 | |||||
| chr11:47097297
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0056 | 2 | HG01934.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.281-40348A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097297 | ||||||
| chr11:47097324
|
TGGGGGGG others(119): Show |
T | 2 | a0001c0001t0001g0019a0001c0001t0001g0056 | 2 | HG01934.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.281-40320_281-4019 others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097324 | ||||||
| chr11:47097342
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0122 | 2 | HG03710.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.281-40303G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097342 | ||||||
| chr11:47097362
|
TGGGAGGT others(123): Show |
T | 17 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(14): Show | 17 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.281-40186_281-4005 others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097362 | |||||
| chr11:47097419
|
T | TGCCCGGC others(42): Show |
106 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(103): Show | 106 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.281-40187_281-4018 others(53): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097419 | |||||
| chr11:47097419
|
T | TGCCCGGC others(270): Show |
1 | a0001c0001t0001g0148 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.281-40187_281-4018 others(281): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097419 | |||||
| chr11:47097419
|
TGCCCGGC others(172): Show |
T | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.281-40186_281-4000 others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097419 | |||||
| chr11:47097451
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0056 | 2 | HG01934.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.281-40194T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097451 | ||||||
| chr11:47097451
|
T | TGGGGGGG others(43): Show |
1 | a0001c0001t0001g0054 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.281-40187_281-4018 others(54): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097451 | |||||
| chr11:47097451
|
T | TGGGGGGG others(43): Show |
11 | a0001c0001t0001g0112a0001c0001t0001g0142a0001c0001t0001g0151others(8): Show | 11 | HG00597.hp2 HG00735.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.281-40187_281-4018 others(54): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097451 | |||||
| chr11:47097452
|
G | C | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(51): Show | 54 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.281-40193G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097452 | ||||||
| chr11:47097452
|
G | GGGGGGGT others(41): Show |
1 | a0001c0001t0001g0127 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.281-40187_281-4018 others(52): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097452 | |||||
| chr11:47097452
|
G | GGGGGGGT others(42): Show |
21 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(18): Show | 21 | HG00735.hp2 HG01074.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.281-40187_281-4018 others(53): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097452 | |||||
| chr11:47097468
|
CCCTGCCC others(121): Show |
C | 1 | a0001c0005t0001g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-40174_281-4004 others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097468 | |||||
| chr11:47097493
|
G | A | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.281-40152G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097493 | ||||||
| chr11:47097596
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(216): Show | 219 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(216): Show |
intron_variant | MODIFIER | c.281-40049T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097596 | ||||||
| chr11:47097612
|
C | A | 1 | a0001c0001t0001g0001 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.281-40033C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097612 | ||||||
| chr11:47097640
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.281-40005G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097640 | ||||||
| chr11:47097679
|
TG | T | 101 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(98): Show | 101 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.281-39957delG | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097679 | |||||
| chr11:47097684
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 74 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.281-39961G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097684 | ||||||
| chr11:47097690
|
C | T | 5 | a0001c0001t0001g0125a0001c0001t0001g0143a0001c0001t0001g0151others(2): Show | 5 | HG01934.hp1 HG01975.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-39955C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097690 | ||||||
| chr11:47097710
|
C | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 97 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.281-39935C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097710 | ||||||
| chr11:47097748
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-39897C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097748 | ||||||
| chr11:47097762
|
A | C | 1 | a0001c0001t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.281-39883A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097762 | ||||||
| chr11:47097867
|
C | A | 121 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(118): Show | 121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.281-39778C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097867 | ||||||
| chr11:47098253
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.281-39392C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47098253 | ||||||
| chr11:47098324
|
A | T | 122 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(119): Show | 122 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.281-39321A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47098324 | ||||||
| chr11:47098504
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-39141T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47098504 | ||||||
| chr11:47098507
|
CT | C | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(53): Show | 56 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.281-39123delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47098507 | |||||
| chr11:47098512
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.281-39133T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47098512 | ||||||
| chr11:47098515
|
T | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0018others(7): Show | 10 | HG00735.hp2 HG01074.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.281-39130T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47098515 | ||||||
| chr11:47098748
|
C | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 74 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.281-38897C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47098748 | ||||||
| chr11:47098778
|
A | T | 1 | a0001c0001t0001g0204 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.281-38867A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47098778 | ||||||
| chr11:47099139
|
C | A | 1 | a0001c0001t0001g0021 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.281-38506C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47099139 | ||||||
| chr11:47099347
|
C | A | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-38298C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47099347 | ||||||
| chr11:47099516
|
C | A | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-38129C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47099516 | ||||||
| chr11:47099625
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 74 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.281-38020T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47099625 | ||||||
| chr11:47099857
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.281-37788G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47099857 | ||||||
| chr11:47099883
|
A | C | 1 | a0001c0005t0001g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-37762A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47099883 | ||||||
| chr11:47099996
|
C | G | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(53): Show | 56 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.281-37649C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47099996 | ||||||
| chr11:47100107
|
T | C | 9 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0177others(6): Show | 9 | HG02647.hp1 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.281-37538T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47100107 | ||||||
| chr11:47100201
|
A | T | 1 | a0001c0001t0002g0207 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.281-37444A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47100201 | ||||||
| chr11:47100331
|
T | A | 1 | a0001c0001t0001g0122 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.281-37314T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47100331 | ||||||
| chr11:47100476
|
A | C | 1 | a0001c0001t0001g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.281-37169A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47100476 | ||||||
| chr11:47100541
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.281-37104T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47100541 | ||||||
| chr11:47100871
|
GC | G | 121 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(118): Show | 121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.281-36773delC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47100871 | ||||||
| chr11:47101002
|
A | AT | 27 | a0001c0001t0001g0001a0001c0001t0001g0116a0001c0001t0001g0191others(24): Show | 27 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.281-36628dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101002 | |||||
| chr11:47101164
|
A | AT | 25 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(22): Show | 25 | HG00621.hp1 HG01109.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.281-36456dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | |||||
| chr11:47101164
|
A | ATT | 9 | a0001c0001t0001g0077a0001c0001t0001g0173a0001c0001t0001g0195others(6): Show | 9 | HG01109.hp1 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.281-36457_281-3645 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | |||||
| chr11:47101164
|
A | ATTT | 9 | a0001c0001t0001g0179a0001c0001t0001g0186a0001c0001t0001g0191others(6): Show | 9 | HG02109.hp1 HG02818.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.281-36458_281-3645 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | |||||
| chr11:47101164
|
A | ATTTT | 8 | a0001c0001t0001g0147a0001c0001t0001g0162a0001c0001t0001g0197others(5): Show | 8 | HG01261.hp1 HG02293.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-36459_281-3645 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | |||||
| chr11:47101164
|
A | ATTTTT | 20 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0104others(17): Show | 20 | HG01257.hp2 HG01358.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.281-36460_281-3645 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | |||||
| chr11:47101164
|
A | ATTTTTT | 17 | a0001c0001t0001g0089a0001c0001t0001g0095a0001c0001t0001g0096others(14): Show | 17 | HG00280.hp2 HG00597.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.281-36461_281-3645 others(10): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | |||||
| chr11:47101164
|
A | ATTTTTTT | 8 | a0001c0001t0001g0082a0001c0001t0001g0127a0001c0001t0001g0145others(5): Show | 8 | HG00733.hp2 HG02647.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-36462_281-3645 others(11): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | |||||
| chr11:47101164
|
A | ATTTTTTT others(1): Show |
6 | a0001c0001t0001g0124a0001c0001t0001g0137a0001c0001t0001g0139others(3): Show | 6 | HG01081.hp1 HG01496.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-36463_281-3645 others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | |||||
| chr11:47101164
|
A | ATTTTTTT others(2): Show |
16 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(13): Show | 16 | HG00438.hp1 HG00438.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.281-36464_281-3645 others(13): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | |||||
| chr11:47101164
|
A | ATTTTTTT others(3): Show |
4 | a0001c0001t0001g0143a0001c0001t0001g0155a0001c0001t0001g0159others(1): Show | 4 | HG00673.hp1 HG01361.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-36465_281-3645 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | |||||
| chr11:47101164
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0122 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.281-36466_281-3645 others(15): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | |||||
| chr11:47101164
|
A | ATTTTTTT others(5): Show |
2 | a0001c0001t0001g0156a0001c0001t0001g0168 | 2 | HG00735.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.281-36467_281-3645 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | |||||
| chr11:47101164
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0132 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.281-36468_281-3645 others(17): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | |||||
| chr11:47101164
|
A | ATTTTTTT others(7): Show |
2 | a0001c0001t0001g0121a0001c0001t0001g0189 | 2 | HG00738.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.281-36469_281-3645 others(18): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | |||||
| chr11:47101164
|
A | ATTTTTTT others(9): Show |
1 | a0001c0001t0001g0187 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.281-36471_281-3645 others(20): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | |||||
| chr11:47101164
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0184 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.281-36472_281-3645 others(21): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | |||||
| chr11:47101164
|
A | ATTTTTTT others(16): Show |
1 | a0001c0001t0001g0175 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.281-36478_281-3645 others(27): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | |||||
| chr11:47101185
|
TTTTTATT others(3): Show |
T | 1 | a0005c0006t0001g0200 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.281-36455_281-3644 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101185 | |||||
| chr11:47101188
|
T | A | 1 | a0001c0001t0001g0006 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.281-36457T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47101188 | ||||||
| chr11:47101189
|
TA | T | 28 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(25): Show | 28 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.281-36455delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47101189 | ||||||
| chr11:47101190
|
A | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(184): Show | 187 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.281-36455A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47101190 | ||||||
| chr11:47101195
|
A | T | 141 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0076others(138): Show | 141 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.281-36450A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47101195 | ||||||
| chr11:47101318
|
T | A | 1 | a0001c0001t0001g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.281-36327T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47101318 | ||||||
| chr11:47101402
|
G | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.281-36243G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47101402 | ||||||
| chr11:47101439
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.281-36206T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47101439 | ||||||
| chr11:47102048
|
G | A | 3 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0135 | 3 | NA18960.hp2 NA18978.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.281-35597G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47102048 | ||||||
| chr11:47102128
|
T | C | 2 | a0002c0002t0001g0086a0002c0002t0001g0087 | 2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.281-35517T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47102128 | ||||||
| chr11:47102183
|
A | G | 4 | a0001c0001t0001g0175a0001c0001t0001g0184a0001c0001t0001g0187others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-35462A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47102183 | ||||||
| chr11:47102314
|
A | C | 1 | a0001c0001t0001g0144 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.281-35331A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47102314 | ||||||
| chr11:47102640
|
T | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.281-35005T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47102640 | ||||||
| chr11:47102731
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0072 | 2 | NA18964.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.281-34914G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47102731 | ||||||
| chr11:47102774
|
G | C | 1 | a0001c0001t0001g0115 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.281-34871G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47102774 | ||||||
| chr11:47102989
|
G | GA | 124 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(121): Show | 124 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.281-34638dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47102989 | |||||
| chr11:47102989
|
G | GAA | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.281-34639_281-3463 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47102989 | |||||
| chr11:47102989
|
G | GAAA | 12 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(9): Show | 12 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.281-34640_281-3463 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47102989 | |||||
| chr11:47103110
|
A | T | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.281-34535A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47103110 | ||||||
| chr11:47103399
|
C | CA | 74 | a0001c0001t0001g0031a0001c0001t0001g0071a0001c0001t0001g0082others(71): Show | 74 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.281-34231dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47103399 | |||||
| chr11:47103590
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.281-34055T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47103590 | ||||||
| chr11:47103608
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.281-34037C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47103608 | ||||||
| chr11:47103662
|
A | C | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-33983A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47103662 | ||||||
| chr11:47103670
|
C | CT | 5 | a0001c0001t0001g0013a0001c0001t0001g0213a0001c0001t0002g0206others(2): Show | 5 | HG01109.hp2 HG02055.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-33951dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47103670 | |||||
| chr11:47103670
|
CT | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 151 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.281-33951delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47103670 | |||||
| chr11:47103778
|
G | A | 1 | a0001c0005t0001g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-33867G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47103778 | ||||||
| chr11:47103806
|
C | T | 16 | a0001c0001t0001g0091a0001c0001t0001g0102a0001c0001t0001g0106others(13): Show | 16 | HG00609.hp1 HG00738.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.281-33839C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47103806 | ||||||
| chr11:47103838
|
C | T | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-33807C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47103838 | ||||||
| chr11:47103851
|
T | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0116others(4): Show | 7 | HG00621.hp2 HG02080.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-33794T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47103851 | ||||||
| chr11:47104004
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.281-33641T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47104004 | ||||||
| chr11:47104081
|
T | G | 121 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(118): Show | 121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.281-33564T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47104081 | ||||||
| chr11:47104096
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.281-33549A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47104096 | ||||||
| chr11:47104200
|
G | C | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-33445G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47104200 | ||||||
| chr11:47104735
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.281-32910C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47104735 | ||||||
| chr11:47105114
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.281-32531T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47105114 | ||||||
| chr11:47105391
|
C | T | 1 | a0001c0001t0003g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.281-32254C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47105391 | ||||||
| chr11:47105602
|
A | G | 7 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0122others(4): Show | 7 | HG00438.hp1 HG02698.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.281-32043A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47105602 | ||||||
| chr11:47105803
|
T | G | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.281-31842T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47105803 | ||||||
| chr11:47105960
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0130 | 2 | HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.281-31685T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47105960 | ||||||
| chr11:47105998
|
G | T | 19 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(16): Show | 19 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.281-31647G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47105998 | ||||||
| chr11:47106155
|
G | A | 18 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(15): Show | 18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.281-31490G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47106155 | ||||||
| chr11:47106376
|
A | G | 3 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG01071.hp2 HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.281-31269A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47106376 | ||||||
| chr11:47106488
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG02698.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.281-31157C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47106488 | ||||||
| chr11:47106642
|
C | CA | 20 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(17): Show | 20 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.281-30991dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47106642 | |||||
| chr11:47106704
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.281-30941G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47106704 | ||||||
| chr11:47106737
|
G | A | 14 | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0001t0001g0043others(11): Show | 14 | HG01361.hp2 HG01975.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.281-30908G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47106737 | ||||||
| chr11:47106795
|
TAACCAAG others(6): Show |
T | 1 | a0001c0001t0001g0068 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.281-30847_281-3083 others(17): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47106795 | |||||
| chr11:47107066
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.281-30579T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47107066 | ||||||
| chr11:47107177
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.281-30468G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47107177 | ||||||
| chr11:47107480
|
T | A | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-30165T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47107480 | ||||||
| chr11:47107846
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 74 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.281-29799C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47107846 | ||||||
| chr11:47107855
|
T | TC | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 97 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.281-29783dupC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47107855 | |||||
| chr11:47107941
|
C | G | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.281-29704C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47107941 | ||||||
| chr11:47108303
|
A | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 74 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.281-29342A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47108303 | ||||||
| chr11:47108415
|
C | G | 1 | a0001c0001t0001g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.281-29230C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47108415 | ||||||
| chr11:47108540
|
C | A | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-29105C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47108540 | ||||||
| chr11:47108704
|
C | CT | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(181): Show | 184 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.281-28921dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47108704 | |||||
| chr11:47108704
|
C | CTT | 10 | a0001c0001t0001g0044a0001c0001t0001g0050a0001c0001t0001g0070others(7): Show | 10 | HG00741.hp1 HG00741.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.281-28922_281-2892 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47108704 | |||||
| chr11:47108704
|
CT | C | 20 | a0001c0001t0001g0011a0001c0001t0001g0077a0001c0001t0001g0078others(17): Show | 20 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.281-28921delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47108704 | |||||
| chr11:47108732
|
A | G | 1 | a0001c0001t0003g0126 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.281-28913A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47108732 | ||||||
| chr11:47108761
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.281-28884C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47108761 | ||||||
| chr11:47108810
|
G | A | 4 | a0001c0001t0001g0125a0001c0001t0001g0143a0001c0001t0001g0151others(1): Show | 4 | HG01934.hp1 HG01975.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-28835G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47108810 | ||||||
| chr11:47108989
|
G | C | 102 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(99): Show | 102 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.281-28656G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47108989 | ||||||
| chr11:47108996
|
C | T | 1 | a0001c0001t0001g0022 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.281-28649C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47108996 | ||||||
| chr11:47109082
|
T | C | 4 | a0001c0001t0001g0128a0001c0001t0001g0149a0001c0001t0001g0150others(1): Show | 4 | HG00733.hp2 HG00735.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-28563T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47109082 | ||||||
| chr11:47109227
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 74 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.281-28418G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47109227 | ||||||
| chr11:47109502
|
C | G | 1 | a0001c0001t0001g0142 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.281-28143C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47109502 | ||||||
| chr11:47109502
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.281-28143C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47109502 | ||||||
| chr11:47109779
|
G | T | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.281-27866G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47109779 | ||||||
| chr11:47109957
|
T | G | 1 | a0001c0001t0001g0161 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.281-27688T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47109957 | ||||||
| chr11:47110160
|
C | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-27485C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47110160 | ||||||
| chr11:47110330
|
A | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 97 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.281-27315A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47110330 | ||||||
| chr11:47110470
|
C | G | 2 | a0001c0001t0001g0110a0001c0004t0001g0111 | 2 | HG01071.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.281-27175C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47110470 | ||||||
| chr11:47110581
|
C | A | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.281-27064C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47110581 | ||||||
| chr11:47110628
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.281-27017C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47110628 | ||||||
| chr11:47110688
|
T | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0131a0001c0001t0001g0163 | 3 | HG03942.hp1 NA18983.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.281-26957T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47110688 | ||||||
| chr11:47110890
|
C | CT | 6 | a0001c0001t0001g0102a0001c0001t0001g0106a0001c0001t0001g0164others(3): Show | 6 | HG00738.hp2 HG01109.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-26738dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47110890 | |||||
| chr11:47110890
|
C | CTTTTTTT | 32 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(29): Show | 32 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.281-26744_281-2673 others(11): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47110890 | |||||
| chr11:47110890
|
C | CTTTTTTT others(1): Show |
55 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(52): Show | 55 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.281-26745_281-2673 others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47110890 | |||||
| chr11:47110890
|
C | CTTTTTTT others(2): Show |
7 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0049others(4): Show | 7 | HG01192.hp2 HG02080.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-26746_281-2673 others(13): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47110890 | |||||
| chr11:47110890
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.281-26747_281-2673 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47110890 | |||||
| chr11:47110991
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.281-26654G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47110991 | ||||||
| chr11:47111173
|
A | T | 76 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(73): Show | 76 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.281-26472A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47111173 | ||||||
| chr11:47111209
|
A | C | 19 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(16): Show | 19 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.281-26436A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47111209 | ||||||
| chr11:47111531
|
C | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(219): Show | 222 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.281-26114C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47111531 | ||||||
| chr11:47111570
|
C | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.281-26075C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47111570 | ||||||
| chr11:47111868
|
C | G | 19 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(16): Show | 19 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.281-25777C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47111868 | ||||||
| chr11:47112053
|
C | G | 18 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(15): Show | 18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.281-25592C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47112053 | ||||||
| chr11:47112131
|
C | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA18971.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.281-25514C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47112131 | ||||||
| chr11:47112313
|
A | ATTTG | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 97 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.281-25312_281-2530 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47112313 | |||||
| chr11:47112348
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.281-25297G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47112348 | ||||||
| chr11:47112362
|
C | G | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0219 | 3 | HG03516.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.281-25283C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47112362 | ||||||
| chr11:47113357
|
G | C | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.281-24288G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47113357 | ||||||
| chr11:47113806
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-23839A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47113806 | ||||||
| chr11:47113855
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.281-23790G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47113855 | ||||||
| chr11:47114010
|
G | C | 10 | a0001c0001t0001g0191a0001c0001t0001g0201a0001c0001t0001g0202others(7): Show | 10 | HG01261.hp1 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.281-23635G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47114010 | ||||||
| chr11:47114131
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0106a0001c0001t0001g0164 | 3 | HG00738.hp2 HG01358.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.281-23514C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47114131 | ||||||
| chr11:47114328
|
C | T | 14 | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0001t0001g0043others(11): Show | 14 | HG01361.hp2 HG01975.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.281-23317C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47114328 | ||||||
| chr11:47114424
|
C | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(219): Show | 222 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.281-23221C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47114424 | ||||||
| chr11:47114445
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(214): Show | 217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.281-23200A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47114445 | ||||||
| chr11:47114837
|
G | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.281-22808G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47114837 | ||||||
| chr11:47115272
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-22373G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47115272 | ||||||
| chr11:47115512
|
A | T | 2 | a0001c0001t0001g0192a0005c0006t0001g0200 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.281-22133A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47115512 | ||||||
| chr11:47115521
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.281-22124C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47115521 | ||||||
| chr11:47115751
|
A | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(214): Show | 217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.281-21894A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47115751 | ||||||
| chr11:47115752
|
A | T | 1 | a0001c0001t0001g0049 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.281-21893A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47115752 | ||||||
| chr11:47115956
|
A | G | 5 | a0001c0001t0001g0091a0001c0001t0001g0102a0001c0001t0001g0106others(2): Show | 5 | HG00738.hp2 HG01099.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-21689A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47115956 | ||||||
| chr11:47116113
|
T | G | 1 | a0001c0001t0001g0095 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.281-21532T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47116113 | ||||||
| chr11:47116303
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.281-21342G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47116303 | ||||||
| chr11:47116427
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.281-21218C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47116427 | ||||||
| chr11:47116661
|
C | T | 6 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(3): Show | 6 | HG00597.hp1 HG02132.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-20984C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47116661 | ||||||
| chr11:47116675
|
G | GT | 144 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 144 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(141): Show |
intron_variant | MODIFIER | c.281-20948dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47116675 | |||||
| chr11:47116675
|
G | GTT | 20 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0060others(17): Show | 20 | HG00280.hp2 HG00597.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.281-20949_281-2094 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47116675 | |||||
| chr11:47116675
|
GT | G | 25 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0090others(22): Show | 25 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.281-20948delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47116675 | |||||
| chr11:47116675
|
GTTT | G | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-20950_281-2094 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47116675 | |||||
| chr11:47116805
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.281-20840G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47116805 | ||||||
| chr11:47117142
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.281-20503T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47117142 | ||||||
| chr11:47117489
|
C | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-20156C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47117489 | ||||||
| chr11:47117512
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-20133T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47117512 | ||||||
| chr11:47117703
|
T | C | 5 | a0001c0001t0001g0091a0001c0001t0001g0102a0001c0001t0001g0106others(2): Show | 5 | HG00738.hp2 HG01099.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-19942T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47117703 | ||||||
| chr11:47117862
|
C | T | 1 | a0001c0005t0001g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-19783C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47117862 | ||||||
| chr11:47117877
|
CT | C | 122 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(119): Show | 122 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.281-19746delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47117877 | |||||
| chr11:47117877
|
CTT | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(81): Show | 84 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.281-19747_281-1974 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47117877 | |||||
| chr11:47117883
|
T | C | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-19762T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47117883 | ||||||
| chr11:47117914
|
G | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.281-19731G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47117914 | ||||||
| chr11:47118086
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.281-19559G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47118086 | ||||||
| chr11:47118209
|
T | A | 1 | a0001c0001t0001g0149 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.281-19436T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47118209 | ||||||
| chr11:47118401
|
T | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(219): Show | 222 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.281-19244T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47118401 | ||||||
| chr11:47118508
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0186 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.281-19137C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47118508 | ||||||
| chr11:47118526
|
G | C | 1 | a0001c0001t0003g0126 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.281-19119G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47118526 | ||||||
| chr11:47118697
|
T | A | 3 | a0001c0001t0001g0089a0001c0001t0001g0131a0001c0001t0001g0163 | 3 | HG03942.hp1 NA18983.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.281-18948T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47118697 | ||||||
| chr11:47118810
|
T | G | 1 | a0001c0001t0001g0021 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.281-18835T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47118810 | ||||||
| chr11:47119039
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.281-18606T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47119039 | ||||||
| chr11:47119186
|
G | C | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-18459G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47119186 | ||||||
| chr11:47119278
|
A | T | 1 | a0001c0005t0001g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-18367A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47119278 | ||||||
| chr11:47119602
|
CT | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(47): Show | 50 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.281-18017delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47119602 | |||||
| chr11:47119602
|
CTT | C | 113 | a0001c0001t0001g0015a0001c0001t0001g0074a0001c0001t0001g0076others(110): Show | 113 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.281-18018_281-1801 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47119602 | |||||
| chr11:47119681
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(63): Show | 66 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.281-17964G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47119681 | ||||||
| chr11:47119705
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.281-17940G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47119705 | ||||||
| chr11:47119749
|
T | A | 1 | a0001c0001t0001g0023 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.281-17896T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47119749 | ||||||
| chr11:47119812
|
C | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(219): Show | 222 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.281-17833C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47119812 | ||||||
| chr11:47119945
|
C | T | 8 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0116others(5): Show | 8 | HG00621.hp2 HG02080.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.281-17700C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47119945 | ||||||
| chr11:47120119
|
C | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 97 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.281-17526C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47120119 | ||||||
| chr11:47120515
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.281-17130G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47120515 | ||||||
| chr11:47120634
|
C | A | 4 | a0001c0001t0001g0175a0001c0001t0001g0184a0001c0001t0001g0187others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-17011C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47120634 | ||||||
| chr11:47120695
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-16950C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47120695 | ||||||
| chr11:47120833
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0153 | 2 | HG00738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.281-16812A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47120833 | ||||||
| chr11:47121111
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.281-16534A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47121111 | ||||||
| chr11:47121573
|
T | G | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-16072T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47121573 | ||||||
| chr11:47121796
|
G | T | 1 | a0001c0001t0001g0019 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.281-15849G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47121796 | ||||||
| chr11:47122069
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.281-15576C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122069 | ||||||
| chr11:47122069
|
C | CA | 6 | a0001c0001t0001g0076a0001c0001t0001g0176a0001c0001t0001g0177others(3): Show | 6 | HG02451.hp2 HG02809.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-15553dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | |||||
| chr11:47122069
|
C | CAAA | 5 | a0001c0001t0001g0091a0001c0001t0001g0174a0001c0001t0001g0180others(2): Show | 5 | HG01099.hp2 HG02559.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-15555_281-1555 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | |||||
| chr11:47122069
|
C | CAAAA | 6 | a0001c0001t0001g0175a0001c0001t0001g0184a0001c0001t0002g0196others(3): Show | 6 | HG01071.hp1 HG01243.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.281-15556_281-1555 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | |||||
| chr11:47122069
|
C | CAAAAA | 10 | a0001c0001t0001g0102a0001c0001t0001g0106a0001c0001t0001g0109others(7): Show | 10 | HG00738.hp2 HG01109.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.281-15557_281-1555 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | |||||
| chr11:47122069
|
C | CAAAAAAA others(3): Show |
1 | a0002c0002t0001g0087 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.281-15562_281-1555 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | |||||
| chr11:47122069
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0120 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.281-15564_281-1555 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | |||||
| chr11:47122069
|
CAA | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(5): Show | 8 | HG01081.hp2 HG01099.hp1 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-15554_281-1555 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | |||||
| chr11:47122069
|
CAAAA | C | 42 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(39): Show | 42 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.281-15556_281-1555 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | |||||
| chr11:47122069
|
CAAAAAAA | C | 5 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(2): Show | 5 | HG01515.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-15559_281-1555 others(11): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | |||||
| chr11:47122087
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0118 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.281-15557_281-1555 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122087 | |||||
| chr11:47122087
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0121 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.281-15558_281-1555 others(25): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122087 | ||||||
| chr11:47122087
|
A | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0052a0001c0001t0001g0054others(1): Show | 4 | HG01074.hp2 HG01261.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-15558A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122087 | ||||||
| chr11:47122089
|
A | AATATATA others(3): Show |
2 | a0001c0001t0001g0145a0001c0001t0001g0156 | 2 | HG00735.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.281-15555_281-1555 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122089 | |||||
| chr11:47122089
|
A | AATATATA others(5): Show |
2 | a0001c0001t0001g0161a0003c0003t0001g0113 | 2 | HG00597.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.281-15555_281-1555 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122089 | |||||
| chr11:47122089
|
A | AATATATA others(7): Show |
1 | a0001c0001t0001g0159 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.281-15555_281-1555 others(18): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122089 | |||||
| chr11:47122089
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0092a0001c0001t0001g0153 | 2 | HG03688.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.281-15556_281-1555 others(15): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122089 | ||||||
| chr11:47122089
|
A | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(8): Show | 11 | HG00621.hp2 HG00735.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.281-15556A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122089 | ||||||
| chr11:47122089
|
AAAAT | A | 5 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0056others(2): Show | 5 | HG00280.hp1 HG00733.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-15554_281-1555 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122089 | |||||
| chr11:47122091
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0073 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(19): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0001g0047 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(21): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0003g0093 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.281-15553_281-1555 others(18): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(28): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAA others(6): Show |
3 | a0001c0001t0001g0099a0001c0001t0003g0100a0001c0001t0003g0126 | 3 | HG01081.hp1 HG01192.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.281-15553_281-1555 others(17): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(25): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAA others(5): Show |
2 | a0001c0001t0001g0094a0001c0001t0001g0168 | 2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.281-15553_281-1555 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0090 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.281-15553_281-1555 others(18): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0004g0220 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.281-15553_281-1555 others(26): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0223 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.281-15553_281-1555 others(28): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAA others(6): Show |
4 | a0001c0001t0001g0083a0001c0001t0001g0107a0001c0001t0003g0097others(1): Show | 4 | HG02004.hp2 HG03710.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-15553_281-1555 others(17): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0135 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAA others(4): Show |
1 | a0002c0002t0001g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(15): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0132 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.281-15553_281-1555 others(17): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAA others(1): Show |
6 | a0001c0001t0001g0105a0001c0001t0001g0114a0001c0001t0001g0163others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-15553_281-1555 others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0131 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.281-15553_281-1555 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0149 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAT others(4): Show |
1 | a0001c0001t0001g0160 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(15): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAAAT others(6): Show |
1 | a0001c0001t0001g0123 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(17): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAATA others(5): Show |
1 | a0001c0001t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.281-15553_281-1555 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAAATA others(11): Show |
1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(22): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAATAT | 5 | a0001c0001t0001g0119a0001c0001t0001g0190a0001c0001t0001g0191others(2): Show | 5 | HG00673.hp1 HG03130.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-15553_281-1555 others(11): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAAATAT others(10): Show |
1 | a0001c0001t0001g0167 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(21): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAATATA others(1): Show |
5 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0146others(2): Show | 5 | HG02293.hp2 HG02300.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-15553_281-1555 others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAATATA others(3): Show |
2 | a0001c0001t0001g0095a0001c0001t0001g0157 | 2 | HG03831.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.281-15553_281-1555 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAAATATA others(5): Show |
1 | a0001c0001t0001g0144 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.281-15553_281-1555 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAATATAT others(2): Show |
5 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0117others(2): Show | 5 | HG02080.hp2 HG02698.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-15553_281-1555 others(13): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AAATATAT others(4): Show |
1 | a0001c0001t0001g0138 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(15): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | AATATATA others(5): Show |
2 | a0001c0001t0001g0128a0001c0001t0001g0150 | 2 | HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.281-15537_281-1552 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | |||||
| chr11:47122091
|
A | ATATAT | 2 | a0001c0001t0001g0125a0001c0001t0001g0151 | 2 | HG01993.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.281-15554_281-1555 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122091 | ||||||
| chr11:47122091
|
A | ATATATAT | 2 | a0001c0001t0001g0084a0001c0001t0001g0165 | 2 | HG00438.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.281-15554_281-1555 others(11): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122091 | ||||||
| chr11:47122091
|
A | ATATATAT others(2): Show |
5 | a0001c0001t0001g0082a0001c0001t0001g0124a0001c0001t0001g0137others(2): Show | 5 | HG02809.hp2 NA18947.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-15554_281-1555 others(13): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122091 | ||||||
| chr11:47122091
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0155 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.281-15554_281-1555 others(15): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122091 | ||||||
| chr11:47122091
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0141 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.281-15554_281-1555 others(21): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122091 | ||||||
| chr11:47122091
|
A | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(36): Show | 39 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.281-15554A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122091 | ||||||
| chr11:47122093
|
T | A | 19 | a0001c0001t0001g0076a0001c0001t0001g0091a0001c0001t0001g0129others(16): Show | 19 | HG01099.hp2 HG01109.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.281-15552T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122093 | ||||||
| chr11:47122095
|
T | A | 8 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0176others(5): Show | 8 | HG01109.hp1 HG02809.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-15550T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122095 | ||||||
| chr11:47122097
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.281-15548T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122097 | ||||||
| chr11:47122937
|
A | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.281-14708A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122937 | ||||||
| chr11:47122991
|
A | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(63): Show | 66 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.281-14654A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122991 | ||||||
| chr11:47123385
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.281-14260A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47123385 | ||||||
| chr11:47123521
|
G | A | 99 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(96): Show | 99 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.281-14124G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47123521 | ||||||
| chr11:47123807
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.281-13838C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47123807 | ||||||
| chr11:47123877
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.281-13768G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47123877 | ||||||
| chr11:47123939
|
T | TGA | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 97 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.281-13705_281-1370 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47123939 | |||||
| chr11:47124064
|
TATTGAGA others(21): Show |
T | 1 | a0001c0001t0001g0042 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13579_281-1355 others(32): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47124064 | |||||
| chr11:47124114
|
C | CT | 99 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(96): Show | 99 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.281-13504dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47124114 | |||||
| chr11:47124114
|
C | CTT | 36 | a0001c0001t0001g0047a0001c0001t0001g0083a0001c0001t0001g0090others(33): Show | 36 | HG00438.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.281-13505_281-1350 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47124114 | |||||
| chr11:47124114
|
C | CTTT | 5 | a0001c0001t0001g0010a0001c0001t0001g0073a0001c0001t0001g0120others(2): Show | 5 | HG01192.hp1 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-13506_281-1350 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47124114 | |||||
| chr11:47124114
|
C | CTTTT | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG02622.hp1 HG02723.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-13507_281-1350 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47124114 | |||||
| chr11:47124114
|
C | CTTTTT | 43 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(40): Show | 43 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.281-13508_281-1350 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47124114 | |||||
| chr11:47124114
|
C | CTTTTTT | 20 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0021others(17): Show | 20 | HG00642.hp2 HG00735.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.281-13509_281-1350 others(10): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47124114 | |||||
| chr11:47124122
|
T | TGGGTTTT others(25): Show |
1 | a0001c0001t0001g0042 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13523_281-1352 others(36): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124122 | ||||||
| chr11:47124126
|
T | G | 1 | a0001c0001t0001g0042 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13519T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124126 | ||||||
| chr11:47124130
|
T | G | 1 | a0001c0001t0001g0042 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13515T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124130 | ||||||
| chr11:47124134
|
T | G | 1 | a0001c0001t0001g0042 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13511T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124134 | ||||||
| chr11:47124151
|
G | T | 1 | a0001c0001t0001g0042 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13494G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124151 | ||||||
| chr11:47124160
|
G | A | 1 | a0001c0001t0002g0217 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.281-13485G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124160 | ||||||
| chr11:47124227
|
A | C | 1 | a0001c0001t0001g0042 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13418A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124227 | ||||||
| chr11:47124312
|
C | G | 1 | a0001c0001t0001g0042 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13333C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124312 | ||||||
| chr11:47124313
|
G | C | 1 | a0001c0001t0001g0042 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13332G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124313 | ||||||
| chr11:47124523
|
A | C | 1 | a0001c0005t0001g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-13122A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124523 | ||||||
| chr11:47124629
|
C | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-13016C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124629 | ||||||
| chr11:47124980
|
CA | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0050 | 2 | NA18947.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.281-12664delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124980 | ||||||
| chr11:47125016
|
C | G | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-12629C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47125016 | ||||||
| chr11:47125048
|
C | T | 18 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(15): Show | 18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.281-12597C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47125048 | ||||||
| chr11:47125566
|
C | A | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.281-12079C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47125566 | ||||||
| chr11:47125838
|
A | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 97 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.281-11807A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47125838 | ||||||
| chr11:47125874
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.281-11771G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47125874 | ||||||
| chr11:47125879
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.281-11766C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47125879 | ||||||
| chr11:47125955
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.281-11690T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47125955 | ||||||
| chr11:47125970
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.281-11675T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47125970 | ||||||
| chr11:47126659
|
C | T | 99 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(96): Show | 99 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.281-10986C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47126659 | ||||||
| chr11:47126957
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.281-10688A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47126957 | ||||||
| chr11:47127112
|
G | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0116others(4): Show | 7 | HG00621.hp2 HG02080.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-10533G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47127112 | ||||||
| chr11:47127177
|
C | T | 19 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(16): Show | 19 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.281-10468C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47127177 | ||||||
| chr11:47127848
|
G | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0213 | 2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.281-9797G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47127848 | ||||||
| chr11:47127879
|
A | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(204): Show | 207 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.281-9766A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47127879 | ||||||
| chr11:47127882
|
T | A | 1 | a0001c0001t0001g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.281-9763T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47127882 | ||||||
| chr11:47127945
|
T | C | 1 | a0001c0001t0001g0170 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.281-9700T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47127945 | ||||||
| chr11:47128296
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.281-9349G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47128296 | ||||||
| chr11:47128434
|
C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(4): Show | 7 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.281-9211C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47128434 | ||||||
| chr11:47128626
|
G | A | 19 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(16): Show | 19 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.281-9019G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47128626 | ||||||
| chr11:47128688
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.281-8957T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47128688 | ||||||
| chr11:47128696
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.281-8949T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47128696 | ||||||
| chr11:47128882
|
C | T | 3 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080 | 3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.281-8763C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47128882 | ||||||
| chr11:47129229
|
C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0184a0001c0001t0001g0187 | 3 | HG01243.hp1 HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.281-8416C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47129229 | ||||||
| chr11:47129342
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.281-8303T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47129342 | ||||||
| chr11:47129420
|
T | G | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.281-8225T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47129420 | ||||||
| chr11:47129576
|
C | G | 1 | a0001c0001t0001g0037 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.281-8069C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47129576 | ||||||
| chr11:47130030
|
G | A | 1 | a0001c0001t0001g0031 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.281-7615G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47130030 | ||||||
| chr11:47130201
|
G | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0212 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.281-7444G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47130201 | ||||||
| chr11:47130234
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.281-7411C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47130234 | ||||||
| chr11:47130255
|
C | CA | 9 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0080others(6): Show | 9 | HG01934.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.281-7377dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47130255 | |||||
| chr11:47130346
|
G | A | 19 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(16): Show | 19 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.281-7299G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47130346 | ||||||
| chr11:47130394
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.281-7251G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47130394 | ||||||
| chr11:47130635
|
CCTT | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 74 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.281-7005_281-7003d others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47130635 | |||||
| chr11:47130709
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.281-6936C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47130709 | ||||||
| chr11:47130722
|
G | A | 76 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(73): Show | 76 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.281-6923G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47130722 | ||||||
| chr11:47131466
|
G | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0116others(4): Show | 7 | HG00621.hp2 HG02080.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-6179G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47131466 | ||||||
| chr11:47131702
|
C | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0048others(1): Show | 4 | HG01361.hp2 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-5943C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47131702 | ||||||
| chr11:47131750
|
G | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0119 | 2 | NA18949.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.281-5895G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47131750 | ||||||
| chr11:47131840
|
A | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(219): Show | 222 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.281-5805A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47131840 | ||||||
| chr11:47131848
|
A | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.281-5797A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47131848 | ||||||
| chr11:47131876
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.281-5769C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47131876 | ||||||
| chr11:47131963
|
T | A | 3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0213 | 3 | HG02109.hp1 HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.281-5682T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47131963 | ||||||
| chr11:47132129
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0186 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.281-5516G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47132129 | ||||||
| chr11:47132181
|
C | A | 1 | a0001c0001t0001g0134 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.281-5464C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47132181 | ||||||
| chr11:47132282
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.281-5363C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47132282 | ||||||
| chr11:47132472
|
G | A | 1 | a0003c0003t0001g0113 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.281-5173G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47132472 | ||||||
| chr11:47132963
|
A | G | 13 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(10): Show | 13 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.281-4682A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47132963 | ||||||
| chr11:47133013
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.281-4632A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47133013 | ||||||
| chr11:47133143
|
T | A | 1 | a0001c0001t0001g0144 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.281-4502T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47133143 | ||||||
| chr11:47133408
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.281-4237G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47133408 | ||||||
| chr11:47133412
|
G | C | 1 | a0001c0001t0001g0049 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.281-4233G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47133412 | ||||||
| chr11:47133672
|
A | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.281-3973A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47133672 | ||||||
| chr11:47134214
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.281-3431G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47134214 | ||||||
| chr11:47134214
|
G | C | 18 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.281-3431G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47134214 | ||||||
| chr11:47134435
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.281-3210T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47134435 | ||||||
| chr11:47134510
|
C | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-3135C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47134510 | ||||||
| chr11:47134563
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0171 | 2 | NA18983.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.281-3082C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47134563 | ||||||
| chr11:47134579
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.281-3066G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47134579 | ||||||
| chr11:47134876
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-2769C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47134876 | ||||||
| chr11:47134902
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0050 | 2 | NA18947.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.281-2743A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47134902 | ||||||
| chr11:47135154
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.281-2491G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47135154 | ||||||
| chr11:47135266
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.281-2379T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47135266 | ||||||
| chr11:47135679
|
G | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0116others(4): Show | 7 | HG00621.hp2 HG02080.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-1966G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47135679 | ||||||
| chr11:47135976
|
A | ACT | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(64): Show | 67 | HG00280.hp1 HG00597.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.281-1649_281-1648d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47135976 | |||||
| chr11:47136126
|
T | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 97 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.281-1519T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47136126 | ||||||
| chr11:47136284
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.281-1361G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47136284 | ||||||
| chr11:47136314
|
C | T | 25 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(22): Show | 25 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.281-1331C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47136314 | ||||||
| chr11:47136315
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 97 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.281-1330G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47136315 | ||||||
| chr11:47136367
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.281-1278C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47136367 | ||||||
| chr11:47136369
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.281-1276G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47136369 | ||||||
| chr11:47136497
|
A | C | 1 | a0001c0001t0001g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.281-1148A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47136497 | ||||||
| chr11:47136841
|
A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 74 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.281-804A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47136841 | ||||||
| chr11:47137071
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.281-574A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47137071 | ||||||
| chr11:47137168
|
G | C | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-477G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47137168 | ||||||
| chr11:47137403
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.281-242C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47137403 | ||||||
| chr11:47137502
|
G | A | 56 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(53): Show | 56 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.281-143G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47137502 | ||||||
| chr11:47137895
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.365+166T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47137895 | ||||||
| chr11:47138013
|
C | CCA | 10 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0052others(7): Show | 10 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+296_365+297dup others(2): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138013 | |||||
| chr11:47138015
|
A | C | 7 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(4): Show | 7 | HG02572.hp2 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.365+286A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47138015 | ||||||
| chr11:47138418
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0170others(1): Show | 4 | HG01071.hp1 HG01515.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+689G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47138418 | ||||||
| chr11:47138470
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.365+741G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47138470 | ||||||
| chr11:47138538
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.365+809G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47138538 | ||||||
| chr11:47138758
|
C | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(220): Show | 223 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.365+1029C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47138758 | ||||||
| chr11:47138848
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.365+1119G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47138848 | ||||||
| chr11:47138895
|
G | A | 1 | a0001c0001t0002g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.365+1166G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47138895 | ||||||
| chr11:47138979
|
C | CA | 27 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(24): Show | 27 | HG00642.hp2 HG00735.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.365+1283dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | |||||
| chr11:47138979
|
C | CAA | 19 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0017others(16): Show | 19 | HG00280.hp1 HG00597.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.365+1282_365+1283d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | |||||
| chr11:47138979
|
C | CAAA | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(17): Show | 20 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.365+1281_365+1283d others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | |||||
| chr11:47138979
|
C | CAAAA | 10 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0057others(7): Show | 10 | HG00438.hp2 HG01081.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+1280_365+1283d others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | |||||
| chr11:47138979
|
C | CAAAAA | 8 | a0001c0001t0001g0049a0001c0001t0001g0094a0001c0001t0001g0107others(5): Show | 8 | HG00642.hp1 HG01243.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.365+1279_365+1283d others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | |||||
| chr11:47138979
|
CA | C | 39 | a0001c0001t0001g0010a0001c0001t0001g0074a0001c0001t0001g0076others(36): Show | 39 | HG00280.hp2 HG00597.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.365+1283delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | |||||
| chr11:47138979
|
CAA | C | 73 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0091others(70): Show | 73 | HG00438.hp1 HG00609.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.365+1282_365+1283d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | |||||
| chr11:47138979
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0128 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.365+1268_365+1283d others(18): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | |||||
| chr11:47138979
|
CAAAAAAA others(14): Show |
C | 1 | a0001c0001t0001g0114 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.365+1263_365+1283d others(23): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | |||||
| chr11:47139072
|
C | T | 99 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(96): Show | 99 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.365+1343C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47139072 | ||||||
| chr11:47139364
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.365+1635C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47139364 | ||||||
| chr11:47139421
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.365+1692C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47139421 | ||||||
| chr11:47139671
|
C | CA | 6 | a0001c0001t0001g0010a0001c0001t0001g0102a0001c0001t0001g0221others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.365+1957dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47139671 | |||||
| chr11:47139671
|
CA | C | 53 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(50): Show | 53 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.365+1957delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47139671 | |||||
| chr11:47139861
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.365+2132C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47139861 | ||||||
| chr11:47140012
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.365+2283T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47140012 | ||||||
| chr11:47140096
|
C | T | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.365+2367C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47140096 | ||||||
| chr11:47140704
|
GC | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(220): Show | 223 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.365+2977delC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47140704 | |||||
| chr11:47140970
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.365+3241G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47140970 | ||||||
| chr11:47140996
|
G | C | 1 | a0001c0001t0002g0207 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.365+3267G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47140996 | ||||||
| chr11:47141053
|
T | G | 102 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(99): Show | 102 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.365+3324T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47141053 | ||||||
| chr11:47141129
|
T | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0066 | 2 | HG03017.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.365+3400T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47141129 | ||||||
| chr11:47141194
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.365+3465A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47141194 | ||||||
| chr11:47141367
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.365+3638G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47141367 | ||||||
| chr11:47141766
|
C | T | 1 | a0001c0001t0003g0093 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.365+4037C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47141766 | ||||||
| chr11:47141788
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.365+4059C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47141788 | ||||||
| chr11:47141932
|
C | CA | 87 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0034others(84): Show | 87 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.365+4229dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47141932 | |||||
| chr11:47141932
|
C | CAA | 35 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0084others(32): Show | 35 | HG00438.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.365+4228_365+4229d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47141932 | |||||
| chr11:47141932
|
CA | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0018others(20): Show | 23 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.365+4229delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47141932 | |||||
| chr11:47141932
|
CAA | C | 10 | a0001c0001t0001g0073a0001c0001t0001g0090a0001c0001t0001g0099others(7): Show | 10 | HG01081.hp1 HG01496.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.365+4228_365+4229d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47141932 | |||||
| chr11:47141932
|
CAAAAA | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.365+4225_365+4229d others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47141932 | |||||
| chr11:47141971
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.365+4242G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47141971 | ||||||
| chr11:47142191
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.365+4462C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47142191 | ||||||
| chr11:47142241
|
CA | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(213): Show | 216 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(213): Show |
intron_variant | MODIFIER | c.365+4528delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47142241 | |||||
| chr11:47142261
|
T | G | 2 | a0001c0001t0001g0221a0001c0001t0004g0220 | 2 | HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.365+4532T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47142261 | ||||||
| chr11:47142573
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.365+4844G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47142573 | ||||||
| chr11:47142657
|
G | C | 149 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(146): Show | 149 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.365+4928G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47142657 | ||||||
| chr11:47142888
|
T | A | 1 | a0001c0001t0001g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.365+5159T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47142888 | ||||||
| chr11:47143555
|
G | A | 99 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(96): Show | 99 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.365+5826G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47143555 | ||||||
| chr11:47143597
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.365+5868C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47143597 | ||||||
| chr11:47143814
|
A | G | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.365+6085A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47143814 | ||||||
| chr11:47144270
|
C | G | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+6541C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47144270 | ||||||
| chr11:47144698
|
G | C | 5 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0137others(2): Show | 5 | HG00438.hp1 NA18947.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.365+6969G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47144698 | ||||||
| chr11:47144800
|
T | A | 7 | a0001c0001t0001g0191a0001c0001t0001g0201a0001c0001t0001g0202others(4): Show | 7 | HG01261.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.365+7071T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47144800 | ||||||
| chr11:47144980
|
A | AT | 20 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(17): Show | 20 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.365+7277dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47144980 | |||||
| chr11:47144980
|
A | ATT | 49 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(46): Show | 49 | HG00280.hp2 HG00438.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.365+7276_365+7277d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47144980 | |||||
| chr11:47144980
|
A | ATTT | 24 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0105others(21): Show | 24 | HG00597.hp2 HG01243.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.365+7275_365+7277d others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47144980 | |||||
| chr11:47144980
|
ATT | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0049others(9): Show | 12 | HG00621.hp1 HG01978.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.365+7276_365+7277d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47144980 | |||||
| chr11:47144980
|
ATTT | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(80): Show | 83 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.365+7275_365+7277d others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47144980 | |||||
| chr11:47144980
|
ATTTTTTT others(7): Show |
A | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.365+7264_365+7277d others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47144980 | |||||
| chr11:47145135
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.365+7406G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47145135 | ||||||
| chr11:47145328
|
G | A | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+7599G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47145328 | ||||||
| chr11:47145900
|
A | ATTATT | 4 | a0001c0001t0001g0043a0001c0001t0001g0095a0001c0001t0001g0190others(1): Show | 4 | HG00673.hp1 HG02300.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+8200_365+8204d others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47145900 | |||||
| chr11:47145900
|
A | ATTGTT | 25 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(22): Show | 25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.365+8173_365+8174i others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47145900 | |||||
| chr11:47146119
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.365+8390T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47146119 | ||||||
| chr11:47146152
|
C | G | 18 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(15): Show | 18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.365+8423C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47146152 | ||||||
| chr11:47146238
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 74 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.365+8509G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47146238 | ||||||
| chr11:47146365
|
CA | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(208): Show | 211 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.365+8656delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47146365 | |||||
| chr11:47146658
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.366-8518T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47146658 | ||||||
| chr11:47146703
|
A | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0052others(7): Show | 10 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.366-8473A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47146703 | ||||||
| chr11:47146752
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.366-8424G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47146752 | ||||||
| chr11:47146971
|
G | A | 9 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0177others(6): Show | 9 | HG02647.hp1 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.366-8205G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47146971 | ||||||
| chr11:47147632
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.366-7544G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47147632 | ||||||
| chr11:47147677
|
G | C | 56 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(53): Show | 56 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.366-7499G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47147677 | ||||||
| chr11:47147825
|
T | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.366-7351T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47147825 | ||||||
| chr11:47148004
|
G | A | 19 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(16): Show | 19 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.366-7172G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47148004 | ||||||
| chr11:47148422
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.366-6754C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47148422 | ||||||
| chr11:47148431
|
T | C | 1 | a0001c0005t0001g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.366-6745T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47148431 | ||||||
| chr11:47148896
|
A | G | 1 | a0001c0001t0003g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.366-6280A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47148896 | ||||||
| chr11:47149231
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.366-5945G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47149231 | ||||||
| chr11:47149465
|
T | C | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-5711T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47149465 | ||||||
| chr11:47150163
|
G | A | 6 | a0001c0001t0001g0094a0001c0001t0003g0093a0001c0001t0003g0097others(3): Show | 6 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.366-5013G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47150163 | ||||||
| chr11:47150200
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0119 | 2 | NA18949.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.366-4976C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47150200 | ||||||
| chr11:47150324
|
T | C | 16 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(13): Show | 16 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.366-4852T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47150324 | ||||||
| chr11:47150520
|
A | T | 1 | a0001c0001t0001g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.366-4656A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47150520 | ||||||
| chr11:47150531
|
C | A | 1 | a0001c0005t0001g0085 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.366-4645C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47150531 | ||||||
| chr11:47150571
|
T | G | 1 | a0001c0007t0001g0063 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.366-4605T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47150571 | ||||||
| chr11:47150883
|
GT | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(173): Show | 176 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.366-4272delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47150883 | |||||
| chr11:47151219
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.366-3957C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47151219 | ||||||
| chr11:47151400
|
C | CA | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(73): Show | 76 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.366-3764dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47151400 | |||||
| chr11:47151400
|
CA | C | 16 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(13): Show | 16 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.366-3764delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47151400 | |||||
| chr11:47151505
|
A | G | 12 | a0001c0001t0001g0192a0001c0001t0002g0196a0001c0001t0002g0199others(9): Show | 12 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.366-3671A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47151505 | ||||||
| chr11:47151597
|
C | CG | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(214): Show | 217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.366-3573dupG | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47151597 | |||||
| chr11:47151722
|
T | C | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-3454T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47151722 | ||||||
| chr11:47152024
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.366-3152C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152024 | ||||||
| chr11:47152242
|
C | CA | 12 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(9): Show | 12 | HG00280.hp1 HG01071.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.366-2920dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47152242 | |||||
| chr11:47152242
|
CA | C | 16 | a0001c0001t0001g0076a0001c0001t0001g0172a0001c0001t0001g0174others(13): Show | 16 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.366-2920delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47152242 | |||||
| chr11:47152511
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(73): Show | 76 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.366-2665G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152511 | ||||||
| chr11:47152519
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.366-2657G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152519 | ||||||
| chr11:47152533
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.366-2643G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152533 | ||||||
| chr11:47152535
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.366-2641G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152535 | ||||||
| chr11:47152536
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.366-2640G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152536 | ||||||
| chr11:47152539
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.366-2637G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152539 | ||||||
| chr11:47152576
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.366-2600G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152576 | ||||||
| chr11:47152745
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.366-2431C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152745 | ||||||
| chr11:47152810
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.366-2366C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152810 | ||||||
| chr11:47153199
|
TTA | T | 5 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0137others(2): Show | 5 | HG00438.hp1 NA18947.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.366-1975_366-1974d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47153199 | |||||
| chr11:47153227
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.366-1949T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153227 | ||||||
| chr11:47153293
|
G | T | 1 | a0001c0001t0001g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.366-1883G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153293 | ||||||
| chr11:47153584
|
A | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.366-1592A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153584 | ||||||
| chr11:47153599
|
A | G | 48 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(45): Show | 48 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.366-1577A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153599 | ||||||
| chr11:47153625
|
G | A | 48 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0089others(45): Show | 48 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.366-1551G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153625 | ||||||
| chr11:47153681
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.366-1495C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153681 | ||||||
| chr11:47153776
|
G | A | 71 | a0001c0001t0001g0076a0001c0001t0001g0091a0001c0001t0001g0101others(68): Show | 71 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.366-1400G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153776 | ||||||
| chr11:47153896
|
G | C | 1 | a0001c0001t0001g0001 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.366-1280G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153896 | ||||||
| chr11:47153949
|
G | T | 1 | a0001c0001t0001g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.366-1227G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153949 | ||||||
| chr11:47154258
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.366-918A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47154258 | ||||||
| chr11:47154280
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.366-896G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47154280 | ||||||
| chr11:47154298
|
T | C | 6 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(3): Show | 6 | HG00597.hp1 HG02132.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.366-878T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47154298 | ||||||
| chr11:47154454
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.366-722C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47154454 | ||||||
| chr11:47154455
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.366-721G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47154455 | ||||||
| chr11:47154867
|
A | AC | 7 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0035others(4): Show | 7 | HG01099.hp1 HG01261.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.366-304dupC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47154867 | |||||
| chr11:47155085
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.366-91C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47155085 | ||||||
| chr11:47155453
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.451+192G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 5/8 | chr11 | 47155453 | ||||||
| chr11:47155880
|
A | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(219): Show | 222 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.451+619A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 5/8 | chr11 | 47155880 | ||||||
| chr11:47155956
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.451+695C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 5/8 | chr11 | 47155956 | ||||||
| chr11:47155957
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.451+696G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 5/8 | chr11 | 47155957 | ||||||
| chr11:47156279
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.452-744T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 5/8 | chr11 | 47156279 | ||||||
| chr11:47156286
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.452-737C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 5/8 | chr11 | 47156286 | ||||||
| chr11:47156399
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.452-624A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 5/8 | chr11 | 47156399 | ||||||
| chr11:47156850
|
A | C | 1 | a0001c0001t0001g0035 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.452-173A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 5/8 | chr11 | 47156850 | ||||||
| chr11:47157291
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0119 | 2 | NA18949.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.647+73C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 6/8 | chr11 | 47157291 | ||||||
| chr11:47157305
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.647+87C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 6/8 | chr11 | 47157305 | ||||||
| chr11:47157306
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.647+88G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 6/8 | chr11 | 47157306 | ||||||
| chr11:47157434
|
A | G | 26 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(23): Show | 26 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.647+216A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 6/8 | chr11 | 47157434 | ||||||
| chr11:47157592
|
C | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(167): Show | 170 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(167): Show |
intron_variant | MODIFIER | c.648-221C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 6/8 | chr11 | 47157592 | ||||||
| chr11:47157610
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.648-203C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 6/8 | chr11 | 47157610 | ||||||
| chr11:47158226
|
G | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(8): Show | 11 | HG00642.hp2 HG00733.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.757+304G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47158226 | ||||||
| chr11:47158278
|
A | G | 121 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0084others(118): Show | 121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.757+356A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47158278 | ||||||
| chr11:47158310
|
C | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(167): Show | 170 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(167): Show |
intron_variant | MODIFIER | c.757+388C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47158310 | ||||||
| chr11:47158343
|
G | GA | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(95): Show | 98 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.757+431dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 47158343 | |||||
| chr11:47158621
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.757+699G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47158621 | ||||||
| chr11:47158836
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.757+914G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47158836 | ||||||
| chr11:47158893
|
T | C | 5 | a0001c0001t0003g0093a0001c0001t0003g0097a0001c0001t0003g0098others(2): Show | 5 | HG01081.hp1 HG01192.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.757+971T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47158893 | ||||||
| chr11:47159417
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.757+1495T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47159417 | ||||||
| chr11:47159489
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 94 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.757+1567G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47159489 | ||||||
| chr11:47159500
|
A | T | 18 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(15): Show | 18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.757+1578A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47159500 | ||||||
| chr11:47159776
|
C | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.758-1351C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47159776 | ||||||
| chr11:47159914
|
G | C | 1 | a0001c0001t0003g0097 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.758-1213G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47159914 | ||||||
| chr11:47159936
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.758-1191G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47159936 | ||||||
| chr11:47160299
|
CA | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0017others(21): Show | 24 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.758-807delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 47160299 | |||||
| chr11:47160299
|
CAA | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(134): Show | 137 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.758-808_758-807del others(2): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 47160299 | |||||
| chr11:47160299
|
CAAA | C | 9 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0046others(6): Show | 9 | HG01081.hp1 HG01099.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.758-809_758-807del others(3): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 47160299 | |||||
| chr11:47160556
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.758-571C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47160556 | ||||||
| chr11:47160689
|
A | AT | 20 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0083others(17): Show | 20 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.758-428dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 47160689 | |||||
| chr11:47160757
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.758-370T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47160757 | ||||||
| chr11:47160802
|
A | G | 71 | a0001c0001t0001g0076a0001c0001t0001g0091a0001c0001t0001g0101others(68): Show | 71 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.758-325A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47160802 | ||||||
| chr11:47160817
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.758-310A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47160817 | ||||||
| chr11:47160819
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.758-308G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47160819 | ||||||
| chr11:47161014
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.758-113G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47161014 | ||||||
| chr11:47161073
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.758-54T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47161073 | ||||||
| chr11:47161347
|
T | G | 1 | a0001c0001t0001g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.822-117T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 8/8 | chr11 | 47161347 | ||||||
| chr11:47161375
|
G | A | 21 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0108others(18): Show | 21 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.822-89G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 8/8 | chr11 | 47161375 | ||||||
| chr11:47161434
|
G | A | 11 | a0001c0001t0001g0017a0001c0001t0001g0043a0001c0001t0001g0044others(8): Show | 11 | HG01361.hp2 HG01975.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.822-30G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 8/8 | chr11 | 47161434 |