Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 219931 |
|---|---|
| ensemblid | ENSG00000162341.18 |
| hgncid | 20820 |
| symbol | TPCN2 |
| name | two pore segment channel 2 |
| refseq_nuc | NM_139075.4 |
| refseq_prot | NP_620714.2 |
| ensembl_nuc | ENST00000294309.8 |
| ensembl_prot | ENSP00000294309.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 69048932 |
| end | 69090597 |
| strand | + |
| ver | v1.2 |
| region | chr11:69048932-69090597 |
| region5000 | chr11:69043932-69095597 |
| regionname0 | TPCN2_chr11_69048932_69090597 |
| regionname5000 | TPCN2_chr11_69043932_69095597 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 752 | 119 | 20 | 23 | 74 | 0 | 1 | 54 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002 | 0/1 | 752 | 85 | 19 | 16 | 28 | 4 | 17 | 20 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0003 | 0/0 | 752 | 64 | 4 | 13 | 34 | 8 | 5 | 27 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004 | 0/0 | 752 | 49 | 42 | 2 | 4 | 0 | 1 | 4 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0005 | 0/0 | 752 | 30 | 1 | 10 | 13 | 3 | 3 | 8 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0006 | 0/0 | 752 | 18 | 1 | 9 | 1 | 1 | 6 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0007 | 0/0 | 752 | 8 | 0 | 2 | 6 | 0 | 0 | 4 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0008 | 0/0 | 752 | 6 | 0 | 2 | 0 | 2 | 2 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0009 | 0/0 | 752 | 5 | 0 | 0 | 5 | 0 | 0 | 2 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0010 | 0/0 | 752 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0011 | 0/0 | 752 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0012 | 0/0 | 752 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0013 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0014 | 0/0 | 47 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0015 | 0/0 | 752 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0016 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0017 | 0/0 | 752 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0018 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0019 | 0/0 | 752 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0020 | 0/0 | 402 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0021 | 0/0 | 752 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0022 | 0/0 | 752 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0023 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0024 | 0/0 | 752 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0025 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| 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 | 0/0 | 2259 | 93 | 14 | 16 | 63 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0002 | 0/1 | 2259 | 78 | 13 | 16 | 28 | 3 | 17 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0003 | 0/0 | 2259 | 60 | 4 | 12 | 31 | 8 | 5 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0004 | 0/0 | 2259 | 30 | 1 | 10 | 13 | 3 | 3 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0005 | 0/0 | 2259 | 25 | 6 | 7 | 11 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0006 | 0/0 | 2259 | 21 | 15 | 2 | 4 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0007 | 0/0 | 2259 | 17 | 1 | 9 | 1 | 1 | 5 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0008 | 0/0 | 2259 | 10 | 9 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0009 | 0/0 | 2259 | 8 | 0 | 2 | 6 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0010 | 0/0 | 2259 | 6 | 0 | 2 | 0 | 2 | 2 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0011 | 0/0 | 2259 | 6 | 6 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0012 | 0/0 | 2259 | 5 | 0 | 0 | 5 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0013 | 0/0 | 2259 | 5 | 5 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0014 | 0/0 | 2259 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0015 | 0/0 | 2259 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0016 | 0/0 | 2259 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0017 | 0/0 | 2259 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0018 | 0/0 | 2259 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0019 | 0/0 | 2259 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0020 | 0/0 | 2259 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0021 | 0/0 | 2259 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0022 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0023 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0024 | 0/0 | 2292 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0025 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0026 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0027 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0028 | 0/0 | 2259 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0029 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0030 | 0/0 | 2259 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0031 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0032 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0033 | 0/0 | 2259 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0034 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0035 | 1/0 | 2259 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0036 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0037 | 0/0 | 2259 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0038 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0039 | 0/0 | 2259 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0040 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0041 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0042 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| c0043 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2711 | 84 | 20 | 16 | 26 | 4 | 17 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0002 | 0/0 | 2670 | 70 | 4 | 13 | 40 | 8 | 5 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0003 | 0/0 | 2711 | 45 | 0 | 9 | 36 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0004 | 1/0 | 2711 | 39 | 9 | 8 | 20 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0005 | 0/0 | 2711 | 26 | 3 | 6 | 17 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0006 | 0/0 | 2711 | 22 | 1 | 9 | 1 | 3 | 8 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0007 | 0/0 | 2670 | 18 | 1 | 8 | 3 | 3 | 3 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0008 | 0/0 | 2670 | 12 | 0 | 2 | 10 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0009 | 0/0 | 2704 | 11 | 10 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0010 | 0/0 | 2711 | 8 | 0 | 0 | 8 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0011 | 0/0 | 2711 | 7 | 7 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0012 | 0/0 | 2704 | 7 | 7 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0013 | 0/0 | 2711 | 6 | 6 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0014 | 0/0 | 2711 | 6 | 6 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0015 | 0/0 | 2705 | 5 | 5 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0016 | 0/0 | 2711 | 4 | 3 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0017 | 0/0 | 2711 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0018 | 0/0 | 2670 | 3 | 0 | 0 | 3 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0019 | 0/0 | 2704 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0020 | 0/0 | 2704 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0021 | 0/0 | 2711 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0022 | 0/0 | 2711 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0023 | 0/0 | 2711 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0024 | 0/0 | 2711 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0025 | 0/0 | 2711 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0026 | 0/0 | 2711 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0027 | 0/0 | 2711 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0028 | 0/0 | 2711 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0029 | 0/0 | 2711 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0030 | 0/0 | 2711 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0031 | 0/0 | 2711 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0032 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0033 | 0/0 | 2704 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0034 | 0/0 | 2711 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0035 | 0/0 | 2711 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0036 | 0/0 | 2704 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0037 | 0/0 | 2704 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0038 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0039 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0040 | 0/0 | 2711 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0041 | 0/0 | 2711 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| t0042 | 0/0 | 2711 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| 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 | 9 | 0 | 5 | 4 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0002 | 0/0 | 7 | 0 | 0 | 2 | 0 | 5 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0004 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0005 | 0/0 | 5 | 3 | 1 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0009 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0013 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0014 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0035 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0256 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0306 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| 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 | 0/0 | 2259 | 93 | 14 | 16 | 63 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0001c0005 | 0/0 | 2259 | 25 | 6 | 7 | 11 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0001c0035 | 1/0 | 2259 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0002 | 0/1 | 2259 | 78 | 13 | 16 | 28 | 3 | 17 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0018 | 0/0 | 2259 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0019 | 0/0 | 2259 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0027 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0029 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0033 | 0/0 | 2259 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0003c0003 | 0/0 | 2259 | 60 | 4 | 12 | 31 | 8 | 5 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0003c0020 | 0/0 | 2259 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0003c0025 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0003c0042 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0006 | 0/0 | 2259 | 21 | 15 | 2 | 4 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0008 | 0/0 | 2259 | 10 | 9 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0011 | 0/0 | 2259 | 6 | 6 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0013 | 0/0 | 2259 | 5 | 5 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0015 | 0/0 | 2259 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0016 | 0/0 | 2259 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0023 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0031 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0005c0004 | 0/0 | 2259 | 30 | 1 | 10 | 13 | 3 | 3 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0006c0007 | 0/0 | 2259 | 17 | 1 | 9 | 1 | 1 | 5 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0006c0030 | 0/0 | 2259 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0007c0009 | 0/0 | 2259 | 8 | 0 | 2 | 6 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0008c0010 | 0/0 | 2259 | 6 | 0 | 2 | 0 | 2 | 2 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0009c0012 | 0/0 | 2259 | 5 | 0 | 0 | 5 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0010c0014 | 0/0 | 2259 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0011c0017 | 0/0 | 2259 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0012c0021 | 0/0 | 2259 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0013c0043 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0014c0038 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0015c0037 | 0/0 | 2259 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0016c0036 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0017c0034 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0018c0022 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0019c0032 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0020c0024 | 0/0 | 2292 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0021c0026 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0022c0028 | 0/0 | 2259 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0023c0041 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0024c0039 | 0/0 | 2259 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0025c0040 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0003 | 0/0 | 4969 | 43 | 0 | 9 | 34 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0001c0001t0004 | 0/0 | 4969 | 4 | 1 | 0 | 3 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0001c0001t0005 | 0/0 | 4969 | 26 | 3 | 6 | 17 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0001c0001t0010 | 0/0 | 4969 | 8 | 0 | 0 | 8 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0001c0001t0011 | 0/0 | 4969 | 7 | 7 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0001c0001t0016 | 0/0 | 4969 | 2 | 1 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0001c0001t0022 | 0/0 | 4969 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0001c0001t0035 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0001c0005t0004 | 0/0 | 4969 | 24 | 6 | 6 | 11 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0001c0005t0042 | 0/0 | 4969 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0001c0035t0004 | 1/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0002t0001 | 0/1 | 4969 | 71 | 12 | 16 | 24 | 3 | 15 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0002t0023 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0002t0026 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0002t0027 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0002t0028 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0002t0029 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0002t0030 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0002t0041 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0018t0001 | 0/0 | 4969 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0019t0001 | 0/0 | 4969 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0027t0001 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0029t0001 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0002c0033t0001 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0003c0003t0002 | 0/0 | 4928 | 59 | 4 | 12 | 30 | 8 | 5 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0003c0003t0039 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0003c0020t0002 | 0/0 | 4928 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0003c0025t0002 | 0/0 | 4928 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0003c0042t0002 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0006t0002 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0006t0007 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0006t0009 | 0/0 | 4962 | 10 | 9 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0006t0018 | 0/0 | 4928 | 3 | 0 | 0 | 3 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0006t0019 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0006t0020 | 0/0 | 4962 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0006t0033 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0006t0036 | 0/0 | 4962 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0006t0037 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0008t0001 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0008t0004 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0008t0013 | 0/0 | 4969 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0008t0017 | 0/0 | 4969 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0008t0031 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0008t0034 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0011t0012 | 0/0 | 4962 | 6 | 6 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0013t0015 | 0/0 | 4963 | 5 | 5 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0015t0014 | 0/0 | 4969 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0016t0014 | 0/0 | 4969 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0023t0019 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0004c0031t0012 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0005c0004t0007 | 0/0 | 4928 | 16 | 0 | 7 | 3 | 3 | 3 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0005c0004t0008 | 0/0 | 4928 | 12 | 0 | 2 | 10 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0005c0004t0032 | 0/0 | 4928 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0005c0004t0038 | 0/0 | 4928 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0006c0007t0006 | 0/0 | 4969 | 15 | 1 | 7 | 1 | 1 | 5 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0006c0007t0021 | 0/0 | 4969 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0006c0030t0006 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0007c0009t0004 | 0/0 | 4969 | 8 | 0 | 2 | 6 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0008c0010t0006 | 0/0 | 4969 | 5 | 0 | 2 | 0 | 2 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0008c0010t0024 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0009c0012t0002 | 0/0 | 4928 | 5 | 0 | 0 | 5 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0010c0014t0013 | 0/0 | 4969 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0011c0017t0016 | 0/0 | 4969 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0012c0021t0001 | 0/0 | 4969 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0013c0043t0025 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0014c0038t0009 | 0/0 | 4962 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0015c0037t0001 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0016c0036t0001 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0017c0034t0003 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0018c0022t0001 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0019c0032t0003 | 0/0 | 4969 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0020c0024t0007 | 0/0 | 4961 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0021c0026t0002 | 0/0 | 4928 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0022c0028t0040 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0023c0041t0004 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0024c0039t0006 | 0/0 | 4969 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| a0025c0040t0014 | 0/0 | 4969 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | copy fasta | chr11 | 69043932 | 69095597 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0003g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0010g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0010g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0010g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0010g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0010g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0010g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0010g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0010g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0011g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0011g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0011g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0011g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0011g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0011g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0011g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0016g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0022g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0022g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0001t0035g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0005t0004g0001 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0005t0004g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0005t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0005t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0005t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0005t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0005t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0005t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0005t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0005t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0005t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0005t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0005t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0005t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0005t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0005t0042g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0001c0035t0004g0306 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0002 | 0/0 | 7 | 0 | 0 | 2 | 0 | 5 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0256 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0023g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0026g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0027g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0028g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0029g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0030g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0002t0041g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0018t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0019t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0027t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0029t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0002c0033t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0009 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0013 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0014 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0035 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0003t0039g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0020t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0020t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0025t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0003c0042t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0006t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0006t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0006t0009g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0006t0009g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0006t0009g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0006t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0006t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0006t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0006t0009g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0006t0009g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0006t0018g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0006t0019g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0006t0020g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0006t0033g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0006t0036g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0006t0037g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0008t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0008t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0008t0013g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0008t0013g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0008t0013g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0008t0017g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0008t0017g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0008t0017g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0008t0031g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0008t0034g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0011t0012g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0011t0012g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0011t0012g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0011t0012g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0011t0012g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0011t0012g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0013t0015g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0013t0015g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0013t0015g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0013t0015g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0015t0014g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0015t0014g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0015t0014g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0016t0014g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0016t0014g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0023t0019g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0004c0031t0012g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0007g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0007g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0007g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0007g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0007g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0007g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0007g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0007g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0007g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0007g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0007g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0007g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0007g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0008g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0008g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0008g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0008g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0008g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0008g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0008g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0008g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0008g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0032g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0005c0004t0038g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0006c0007t0006g0004 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0006c0007t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0006c0007t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0006c0007t0006g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0006c0007t0006g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0006c0007t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0006c0007t0006g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0006c0007t0006g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0006c0007t0006g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0006c0007t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0006c0007t0006g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0006c0007t0021g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0006c0030t0006g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0007c0009t0004g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0007c0009t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0007c0009t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0007c0009t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0007c0009t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0008c0010t0006g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0008c0010t0006g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0008c0010t0006g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0008c0010t0006g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0008c0010t0006g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0008c0010t0024g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0009c0012t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0009c0012t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0009c0012t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0009c0012t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0010c0014t0013g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0010c0014t0013g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0010c0014t0013g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0011c0017t0016g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0011c0017t0016g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0012c0021t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0012c0021t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0013c0043t0025g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0014c0038t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0015c0037t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0016c0036t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0017c0034t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0018c0022t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0019c0032t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0020c0024t0007g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0021c0026t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0022c0028t0040g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0023c0041t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0024c0039t0006g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| a0025c0040t0014g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0008 | c0010 | t0006 | g0101 | EUR | GBR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00099 | hp2 | a0005 | c0004 | t0007 | g0146 | EUR | GBR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0255 | EUR | GBR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00140 | hp2 | a0003 | c0003 | t0002 | g0014 | EUR | GBR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0260 | EUR | FIN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00280 | hp2 | a0003 | c0003 | t0002 | g0014 | EUR | FIN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00323 | hp1 | a0008 | c0010 | t0006 | g0102 | EUR | FIN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00323 | hp2 | a0003 | c0003 | t0002 | g0134 | EUR | FIN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00408 | hp2 | a0002 | c0002 | t0027 | g0246 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00423 | hp1 | a0001 | c0005 | t0004 | g0001 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00423 | hp2 | a0003 | c0003 | t0002 | g0144 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00544 | hp1 | a0009 | c0012 | t0002 | g0028 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0278 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00558 | hp1 | a0003 | c0003 | t0002 | g0113 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00558 | hp2 | a0001 | c0001 | t0010 | g0311 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00597 | hp1 | a0001 | c0001 | t0010 | g0284 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00597 | hp2 | a0003 | c0003 | t0002 | g0143 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00609 | hp1 | a0009 | c0012 | t0002 | g0032 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00621 | hp1 | a0005 | c0004 | t0008 | g0010 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00639 | hp1 | a0001 | c0005 | t0042 | g0089 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0227 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0258 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00642 | hp2 | a0005 | c0004 | t0032 | g0163 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | CHS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00733 | hp1 | a0003 | c0003 | t0002 | g0009 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0040 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00735 | hp2 | a0006 | c0007 | t0006 | g0173 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00738 | hp1 | a0003 | c0003 | t0002 | g0131 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0239 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00741 | hp1 | a0005 | c0004 | t0007 | g0269 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0042 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01069 | hp1 | a0007 | c0009 | t0004 | g0001 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0045 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01070 | hp2 | a0005 | c0004 | t0007 | g0037 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0045 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01071 | hp2 | a0005 | c0004 | t0007 | g0037 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01074 | hp2 | a0003 | c0003 | t0002 | g0119 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01081 | hp2 | a0005 | c0004 | t0007 | g0147 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01099 | hp1 | a0003 | c0003 | t0002 | g0133 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0189 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01106 | hp1 | a0005 | c0004 | t0007 | g0154 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01106 | hp2 | a0006 | c0007 | t0006 | g0168 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0262 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01167 | hp1 | a0006 | c0007 | t0006 | g0004 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0042 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01168 | hp1 | a0006 | c0007 | t0021 | g0036 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01168 | hp2 | a0005 | c0004 | t0007 | g0141 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01169 | hp1 | a0006 | c0007 | t0021 | g0036 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01169 | hp2 | a0006 | c0007 | t0006 | g0004 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01175 | hp1 | a0003 | c0003 | t0002 | g0027 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0244 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01192 | hp2 | a0007 | c0009 | t0004 | g0001 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01243 | hp1 | a0003 | c0003 | t0002 | g0013 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01243 | hp2 | a0004 | c0006 | t0036 | g0218 | AMR | PUR | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01255 | hp1 | a0003 | c0003 | t0002 | g0009 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01255 | hp2 | a0020 | c0024 | t0007 | g0179 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01257 | hp1 | a0006 | c0007 | t0006 | g0004 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01257 | hp2 | a0003 | c0003 | t0002 | g0112 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01258 | hp1 | a0006 | c0007 | t0006 | g0004 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01261 | hp1 | a0006 | c0007 | t0006 | g0004 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01261 | hp2 | a0003 | c0003 | t0002 | g0117 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01346 | hp1 | a0003 | c0003 | t0002 | g0034 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01346 | hp2 | a0004 | c0006 | t0009 | g0190 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0257 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01433 | hp2 | a0003 | c0003 | t0002 | g0009 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0274 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01496 | hp2 | a0003 | c0003 | t0002 | g0130 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01515 | hp1 | a0003 | c0003 | t0002 | g0035 | EUR | IBS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01515 | hp2 | a0005 | c0004 | t0007 | g0026 | EUR | IBS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01516 | hp1 | a0002 | c0033 | t0001 | g0040 | EUR | IBS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01516 | hp2 | a0003 | c0003 | t0002 | g0013 | EUR | IBS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01517 | hp1 | a0005 | c0004 | t0007 | g0026 | EUR | IBS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01517 | hp2 | a0003 | c0003 | t0002 | g0013 | EUR | IBS | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01884 | hp1 | a0001 | c0001 | t0011 | g0297 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01884 | hp2 | a0010 | c0014 | t0013 | g0199 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01891 | hp1 | a0002 | c0002 | t0029 | g0224 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01891 | hp2 | a0004 | c0006 | t0009 | g0016 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01928 | hp1 | a0001 | c0005 | t0004 | g0001 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0279 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01934 | hp1 | a0001 | c0001 | t0016 | g0018 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01934 | hp2 | a0003 | c0025 | t0002 | g0136 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01943 | hp1 | a0005 | c0004 | t0008 | g0180 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0280 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01952 | hp1 | a0001 | c0005 | t0004 | g0098 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01952 | hp2 | a0001 | c0005 | t0004 | g0092 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0277 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01975 | hp2 | a0001 | c0005 | t0004 | g0087 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01978 | hp1 | a0001 | c0005 | t0004 | g0001 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0281 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02015 | hp2 | a0001 | c0001 | t0010 | g0309 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02040 | hp2 | a0003 | c0003 | t0039 | g0127 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0275 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02055 | hp2 | a0001 | c0001 | t0011 | g0294 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02071 | hp1 | a0002 | c0002 | t0023 | g0003 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02074 | hp2 | a0009 | c0012 | t0002 | g0114 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02080 | hp2 | a0005 | c0004 | t0007 | g0111 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02083 | hp2 | a0007 | c0009 | t0004 | g0086 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0304 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02129 | hp2 | a0005 | c0004 | t0008 | g0081 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02132 | hp2 | a0003 | c0003 | t0002 | g0032 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02145 | hp1 | a0004 | c0006 | t0019 | g0270 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0263 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0282 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02148 | hp2 | a0008 | c0010 | t0006 | g0025 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02155 | hp1 | a0006 | c0007 | t0006 | g0178 | EAS | CDX | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02155 | hp2 | a0001 | c0001 | t0010 | g0308 | EAS | CDX | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CDX | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02165 | hp2 | a0003 | c0003 | t0002 | g0116 | EAS | CDX | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0235 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02257 | hp2 | a0006 | c0007 | t0006 | g0169 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02258 | hp1 | a0002 | c0018 | t0001 | g0005 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02258 | hp2 | a0004 | c0008 | t0017 | g0183 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02280 | hp1 | a0011 | c0017 | t0016 | g0018 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02280 | hp2 | a0001 | c0001 | t0011 | g0299 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02293 | hp1 | a0005 | c0004 | t0008 | g0122 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02300 | hp2 | a0001 | c0005 | t0004 | g0001 | AMR | PEL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02451 | hp1 | a0004 | c0016 | t0014 | g0050 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02451 | hp2 | a0002 | c0029 | t0001 | g0273 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02523 | hp1 | a0005 | c0004 | t0007 | g0149 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02523 | hp2 | a0007 | c0009 | t0004 | g0001 | EAS | KHV | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02572 | hp2 | a0004 | c0006 | t0009 | g0213 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02615 | hp1 | a0025 | c0040 | t0014 | g0054 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02615 | hp2 | a0001 | c0001 | t0022 | g0302 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02622 | hp1 | a0014 | c0038 | t0009 | g0212 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02622 | hp2 | a0003 | c0003 | t0002 | g0126 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02630 | hp1 | a0004 | c0008 | t0017 | g0106 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02630 | hp2 | a0001 | c0001 | t0016 | g0018 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02683 | hp1 | a0001 | c0005 | t0004 | g0056 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02683 | hp2 | a0003 | c0003 | t0002 | g0014 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02698 | hp2 | a0006 | c0007 | t0006 | g0175 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02717 | hp1 | a0004 | c0006 | t0009 | g0192 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02717 | hp2 | a0023 | c0041 | t0004 | g0088 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02723 | hp1 | a0001 | c0005 | t0004 | g0008 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0276 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02735 | hp1 | a0005 | c0004 | t0007 | g0148 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02735 | hp2 | a0008 | c0010 | t0024 | g0025 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02738 | hp1 | a0006 | c0007 | t0006 | g0177 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0259 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02809 | hp1 | a0004 | c0011 | t0012 | g0204 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02809 | hp2 | a0004 | c0006 | t0033 | g0207 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02818 | hp1 | a0004 | c0006 | t0009 | g0215 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0223 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02886 | hp1 | a0004 | c0008 | t0013 | g0194 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02886 | hp2 | a0004 | c0013 | t0015 | g0208 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02895 | hp1 | a0004 | c0011 | t0012 | g0206 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02895 | hp2 | a0004 | c0006 | t0020 | g0047 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02896 | hp2 | a0004 | c0013 | t0015 | g0038 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02897 | hp1 | a0004 | c0006 | t0020 | g0047 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02897 | hp2 | a0004 | c0013 | t0015 | g0038 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02922 | hp1 | a0005 | c0004 | t0038 | g0139 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0265 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02965 | hp1 | a0001 | c0005 | t0004 | g0008 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02965 | hp2 | a0004 | c0011 | t0012 | g0205 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02970 | hp1 | a0004 | c0006 | t0009 | g0217 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02970 | hp2 | a0001 | c0001 | t0022 | g0303 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02976 | hp1 | a0010 | c0014 | t0013 | g0198 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02976 | hp2 | a0004 | c0023 | t0019 | g0271 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0046 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0220 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03041 | hp1 | a0004 | c0006 | t0009 | g0214 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03041 | hp2 | a0004 | c0006 | t0009 | g0216 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03098 | hp1 | a0001 | c0005 | t0004 | g0008 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03098 | hp2 | a0004 | c0006 | t0009 | g0016 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03130 | hp1 | a0001 | c0001 | t0011 | g0170 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0305 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03139 | hp1 | a0001 | c0005 | t0004 | g0096 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03139 | hp2 | a0004 | c0016 | t0014 | g0049 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03195 | hp1 | a0004 | c0008 | t0013 | g0196 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03195 | hp2 | a0004 | c0011 | t0012 | g0201 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03209 | hp1 | a0002 | c0019 | t0001 | g0039 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03209 | hp2 | a0004 | c0011 | t0012 | g0203 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03225 | hp1 | a0010 | c0014 | t0013 | g0200 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03225 | hp2 | a0002 | c0018 | t0001 | g0005 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0293 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03453 | hp2 | a0011 | c0017 | t0016 | g0285 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0300 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03486 | hp2 | a0004 | c0031 | t0012 | g0202 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0261 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03490 | hp2 | a0005 | c0004 | t0007 | g0142 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0231 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03491 | hp2 | a0006 | c0007 | t0006 | g0171 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03516 | hp1 | a0004 | c0008 | t0013 | g0197 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03516 | hp2 | a0001 | c0005 | t0004 | g0091 | AFR | ESN | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03540 | hp1 | a0004 | c0015 | t0014 | g0052 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0267 | AFR | GWD | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03579 | hp1 | a0016 | c0036 | t0001 | g0187 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03579 | hp2 | a0004 | c0013 | t0015 | g0211 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03654 | hp1 | a0005 | c0004 | t0007 | g0161 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03669 | hp2 | a0003 | c0003 | t0002 | g0129 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | STU | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03688 | hp2 | a0024 | c0039 | t0006 | g0174 | SAS | STU | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03710 | hp1 | a0002 | c0002 | t0041 | g0241 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0254 | SAS | PJL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0234 | SAS | BEB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03831 | hp2 | a0004 | c0008 | t0001 | g0219 | SAS | BEB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03834 | hp1 | a0002 | c0002 | t0030 | g0005 | SAS | BEB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03834 | hp2 | a0006 | c0030 | t0006 | g0167 | SAS | BEB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03942 | hp1 | a0015 | c0037 | t0001 | g0237 | SAS | BEB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03942 | hp2 | a0008 | c0010 | t0006 | g0103 | SAS | BEB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG04115 | hp1 | a0003 | c0003 | t0002 | g0137 | SAS | STU | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG04115 | hp2 | a0003 | c0003 | t0002 | g0128 | SAS | STU | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG04184 | hp1 | a0022 | c0028 | t0040 | g0242 | SAS | BEB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0232 | SAS | BEB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0266 | SAS | STU | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0221 | SAS | STU | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG04228 | hp1 | a0006 | c0007 | t0006 | g0172 | SAS | STU | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG04228 | hp2 | a0003 | c0003 | t0002 | g0027 | SAS | STU | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18522 | hp1 | a0004 | c0013 | t0015 | g0209 | AFR | YRI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18522 | hp2 | a0004 | c0008 | t0004 | g0105 | AFR | YRI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0288 | EAS | CHB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18612 | hp2 | a0003 | c0003 | t0002 | g0035 | EAS | CHB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18747 | hp1 | a0001 | c0001 | t0010 | g0307 | EAS | CHB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18747 | hp2 | a0005 | c0004 | t0008 | g0151 | EAS | CHB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18906 | hp1 | a0018 | c0022 | t0001 | g0240 | AFR | YRI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0291 | AFR | YRI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18939 | hp2 | a0002 | c0002 | t0026 | g0003 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18940 | hp1 | a0003 | c0003 | t0002 | g0029 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0272 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0296 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18942 | hp2 | a0017 | c0034 | t0003 | g0007 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18946 | hp2 | a0005 | c0004 | t0008 | g0109 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18947 | hp1 | a0003 | c0042 | t0002 | g0099 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0287 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18948 | hp1 | a0003 | c0003 | t0002 | g0152 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18950 | hp1 | a0001 | c0005 | t0004 | g0023 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18954 | hp1 | a0003 | c0003 | t0002 | g0030 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18959 | hp1 | a0003 | c0003 | t0002 | g0132 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18962 | hp1 | a0005 | c0004 | t0008 | g0225 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18964 | hp1 | a0012 | c0021 | t0001 | g0222 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18964 | hp2 | a0005 | c0004 | t0008 | g0010 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18966 | hp1 | a0001 | c0001 | t0010 | g0312 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18969 | hp2 | a0009 | c0012 | t0002 | g0165 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18970 | hp1 | a0009 | c0012 | t0002 | g0028 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0048 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18971 | hp1 | a0005 | c0004 | t0008 | g0010 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18973 | hp2 | a0003 | c0003 | t0002 | g0031 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18974 | hp2 | a0003 | c0003 | t0002 | g0181 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18975 | hp1 | a0001 | c0005 | t0004 | g0023 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18975 | hp2 | a0003 | c0003 | t0002 | g0108 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18979 | hp2 | a0001 | c0001 | t0010 | g0310 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0048 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18982 | hp2 | a0003 | c0003 | t0002 | g0030 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18983 | hp2 | a0003 | c0003 | t0002 | g0107 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18985 | hp1 | a0001 | c0005 | t0004 | g0001 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18990 | hp1 | a0003 | c0003 | t0002 | g0029 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18990 | hp2 | a0001 | c0005 | t0004 | g0024 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18993 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18993 | hp2 | a0007 | c0009 | t0004 | g0093 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18997 | hp1 | a0003 | c0003 | t0002 | g0145 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18997 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18999 | hp1 | a0003 | c0003 | t0002 | g0123 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19002 | hp1 | a0003 | c0003 | t0002 | g0110 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19002 | hp2 | a0001 | c0005 | t0004 | g0095 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19004 | hp1 | a0005 | c0004 | t0008 | g0140 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19004 | hp2 | a0001 | c0001 | t0005 | g0292 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19005 | hp1 | a0005 | c0004 | t0008 | g0010 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19005 | hp2 | a0007 | c0009 | t0004 | g0001 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19007 | hp1 | a0005 | c0004 | t0007 | g0162 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19007 | hp2 | a0001 | c0005 | t0004 | g0024 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19009 | hp2 | a0004 | c0006 | t0018 | g0015 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19010 | hp2 | a0003 | c0003 | t0002 | g0033 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19011 | hp1 | a0003 | c0003 | t0002 | g0124 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19011 | hp2 | a0003 | c0003 | t0002 | g0158 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19030 | hp1 | a0004 | c0008 | t0031 | g0195 | AFR | LWK | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19030 | hp2 | a0001 | c0001 | t0011 | g0298 | AFR | LWK | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19043 | hp1 | a0002 | c0019 | t0001 | g0039 | AFR | LWK | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | LWK | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19055 | hp2 | a0001 | c0001 | t0035 | g0313 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19057 | hp1 | a0012 | c0021 | t0001 | g0253 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19057 | hp2 | a0003 | c0003 | t0002 | g0125 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19059 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19059 | hp2 | a0003 | c0003 | t0002 | g0182 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19060 | hp2 | a0003 | c0003 | t0002 | g0120 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19064 | hp1 | a0005 | c0004 | t0008 | g0138 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19065 | hp1 | a0004 | c0006 | t0018 | g0015 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19065 | hp2 | a0021 | c0026 | t0002 | g0193 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19066 | hp1 | a0019 | c0032 | t0003 | g0019 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19066 | hp2 | a0002 | c0002 | t0028 | g0251 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19067 | hp1 | a0001 | c0001 | t0005 | g0283 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19067 | hp2 | a0001 | c0001 | t0005 | g0289 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19068 | hp2 | a0003 | c0020 | t0002 | g0164 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19070 | hp2 | a0004 | c0006 | t0002 | g0159 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19074 | hp1 | a0003 | c0003 | t0002 | g0135 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19075 | hp2 | a0001 | c0005 | t0004 | g0090 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19079 | hp1 | a0003 | c0003 | t0002 | g0033 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19079 | hp2 | a0001 | c0001 | t0010 | g0314 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19080 | hp1 | a0004 | c0006 | t0018 | g0015 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19081 | hp1 | a0007 | c0009 | t0004 | g0084 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19081 | hp2 | a0003 | c0003 | t0002 | g0121 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19082 | hp1 | a0001 | c0005 | t0004 | g0085 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19082 | hp2 | a0003 | c0003 | t0002 | g0153 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19083 | hp1 | a0003 | c0020 | t0002 | g0115 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19085 | hp1 | a0001 | c0005 | t0004 | g0097 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19085 | hp2 | a0001 | c0005 | t0004 | g0094 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19086 | hp2 | a0001 | c0001 | t0005 | g0286 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19090 | hp2 | a0007 | c0009 | t0004 | g0083 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19091 | hp1 | a0003 | c0003 | t0002 | g0031 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0295 | EAS | JPT | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19240 | hp1 | a0004 | c0011 | t0012 | g0210 | AFR | YRI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | YRI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA20129 | hp1 | a0004 | c0006 | t0037 | g0191 | AFR | ASW | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA20129 | hp2 | a0003 | c0003 | t0002 | g0118 | AFR | ASW | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA20752 | hp1 | a0006 | c0007 | t0006 | g0188 | EUR | TSI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA20752 | hp2 | a0003 | c0003 | t0002 | g0009 | EUR | TSI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0228 | EUR | TSI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA20805 | hp2 | a0003 | c0003 | t0002 | g0166 | EUR | TSI | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | GIH | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA20905 | hp2 | a0006 | c0007 | t0006 | g0176 | SAS | GIH | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01123 | hp1 | a0005 | c0004 | t0007 | g0268 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG01123 | hp2 | a0008 | c0010 | t0006 | g0100 | AMR | CLM | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02109 | hp1 | a0003 | c0003 | t0002 | g0160 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0264 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02486 | hp1 | a0001 | c0005 | t0004 | g0008 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02486 | hp2 | a0002 | c0027 | t0001 | g0186 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02559 | hp1 | a0003 | c0003 | t0002 | g0034 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG02559 | hp2 | a0004 | c0015 | t0014 | g0053 | AFR | ACB | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0290 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG03471 | hp2 | a0004 | c0008 | t0017 | g0184 | AFR | MSL | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0301 | AFR | USA | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| HG06807 | hp2 | a0004 | c0015 | t0014 | g0051 | AFR | USA | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA20300 | hp1 | a0004 | c0008 | t0034 | g0185 | AFR | USA | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA20300 | hp2 | a0004 | c0006 | t0009 | g0016 | AFR | USA | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA21309 | hp1 | a0013 | c0043 | t0025 | g0104 | AFR | LWK | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| NA21309 | hp2 | a0004 | c0006 | t0007 | g0150 | AFR | LWK | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0256 | REF | REF | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| homoSapiens_grch38 | hp1 | a0001 | c0035 | t0004 | g0306 | REF | REF | TPCN2_chr11_69043932_69095597 | TPCN2 | chr11 | 69043932 | 69095597 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:69049068
|
C | T | 1 | a0012 | 2 | NA18964.hp1 NA19057.hp1 |
missense_variant | MODERATE | c.71C>T | p.Ala24Val | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/25 | 137/4969 | 71/2259 | 24/752 | chr11 | 69049068 | ||
| chr11:69049077
|
C | G | 1 | a0013 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.80C>G | p.Thr27Ser | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/25 | 146/4969 | 80/2259 | 27/752 | chr11 | 69049077 | ||
| chr11:69054039
|
C | T | 2 | a0024a0025 | 2 | HG02615.hp1 HG03688.hp2 |
missense_variant | MODERATE | c.116C>T | p.Ala39Val | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/25 | 182/4969 | 116/2259 | 39/752 | chr11 | 69054039 | ||
| chr11:69054065
|
C | T | 1 | a0014 | 1 | HG02622.hp1 | stop_gained | HIGH | c.142C>T | p.Gln48* | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/25 | 208/4969 | 142/2259 | 48/752 | chr11 | 69054065 | ||
| chr11:69054782
|
C | T | 1 | a0015 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.236C>T | p.Ser79Leu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/25 | 302/4969 | 236/2259 | 79/752 | chr11 | 69054782 | ||
| chr11:69054787
|
G | A | 1 | a0010 | 3 | HG01884.hp2 HG02976.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.241G>A | p.Val81Ile | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/25 | 307/4969 | 241/2259 | 81/752 | chr11 | 69054787 | ||
| chr11:69054796
|
C | T | 1 | a0009 | 5 | HG00544.hp1 HG00609.hp1 HG02074.hp2 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.250C>T | p.Arg84Trp | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/25 | 316/4969 | 250/2259 | 84/752 | chr11 | 69054796 | ||
| chr11:69055184
|
C | G | 1 | a0016 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.261C>G | p.Ser87Arg | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/25 | 327/4969 | 261/2259 | 87/752 | chr11 | 69055184 | ||
| chr11:69055282
|
C | T | 1 | a0017 | 1 | NA18942.hp2 | missense_variant | MODERATE | c.359C>T | p.Pro120Leu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/25 | 425/4969 | 359/2259 | 120/752 | chr11 | 69055282 | ||
| chr11:69055291
|
G | A | 1 | a0018 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.368G>A | p.Gly123Asp | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/25 | 434/4969 | 368/2259 | 123/752 | chr11 | 69055291 | ||
| chr11:69057635
|
G | T | 1 | a0019 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.487G>T | p.Val163Leu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/25 | 553/4969 | 487/2259 | 163/752 | chr11 | 69057635 | ||
| chr11:69063896
|
G | A | 1 | a0008 | 6 | HG00099.hp1 HG00323.hp1 HG01123.hp2 others(3): Show |
missense_variant&splice_region_variant | MODERATE | c.655G>A | p.Val219Ile | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/25 | 721/4969 | 655/2259 | 219/752 | chr11 | 69063896 | ||
| chr11:69067602
|
G | A | 1 | a0023 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.826G>A | p.Asp276Asn | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/25 | 892/4969 | 826/2259 | 276/752 | chr11 | 69067602 | ||
| chr11:69072692
|
A | G | 6 | a0002a0012a0015others(3): Show | 91 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(88): Show |
missense_variant | MODERATE | c.1127A>G | p.Lys376Arg | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 12/25 | 1193/4969 | 1127/2259 | 376/752 | chr11 | 69072692 | ||
| chr11:69072931
|
G | A | 2 | a0005a0020 | 31 | HG00099.hp2 HG00621.hp1 HG00642.hp2 others(28): Show |
missense_variant | MODERATE | c.1160G>A | p.Gly387Asp | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1226/4969 | 1160/2259 | 387/752 | chr11 | 69072931 | ||
| chr11:69072938
|
T | TCTGAAGG others(26): Show |
1 | a0020 | 1 | HG01255.hp2 | conservative_inframe_insertion | MODERATE | c.1170_1171insAAGGTG others(27): Show |
p.Leu390_Leu391insLy others(31): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1237/4969 | 1171/2259 | 391/752 | INFO_REALIGN_3_PRIME | chr11 | 69072938 | |
| chr11:69072942
|
C | A | 1 | a0020 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1171C>A | p.Leu391Ile | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1237/4969 | 1171/2259 | 391/752 | chr11 | 69072942 | ||
| chr11:69072946
|
C | G | 1 | a0020 | 1 | HG01255.hp2 | stop_gained | HIGH | c.1175C>G | p.Ser392* | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1241/4969 | 1175/2259 | 392/752 | chr11 | 69072946 | ||
| chr11:69072949
|
C | G | 1 | a0020 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1178C>G | p.Ala393Gly | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1244/4969 | 1178/2259 | 393/752 | chr11 | 69072949 | ||
| chr11:69072957
|
T | G | 1 | a0020 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1186T>G | p.Phe396Val | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1252/4969 | 1186/2259 | 396/752 | chr11 | 69072957 | ||
| chr11:69072964
|
A | G | 1 | a0020 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1193A>G | p.Lys398Arg | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1259/4969 | 1193/2259 | 398/752 | chr11 | 69072964 | ||
| chr11:69072986
|
A | C | 1 | a0020 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1215A>C | p.Arg405Ser | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1281/4969 | 1215/2259 | 405/752 | chr11 | 69072986 | ||
| chr11:69072989
|
T | G | 1 | a0020 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1218T>G | p.Ser406Arg | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1284/4969 | 1218/2259 | 406/752 | chr11 | 69072989 | ||
| chr11:69072998
|
A | T | 1 | a0020 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.1227A>T | p.Lys409Asn | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1293/4969 | 1227/2259 | 409/752 | chr11 | 69072998 | ||
| chr11:69073000
|
A | G | 1 | a0020 | 1 | HG01255.hp2 | missense_variant&splice_region_variant | MODERATE | c.1229A>G | p.Glu410Gly | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1295/4969 | 1229/2259 | 410/752 | chr11 | 69073000 | ||
| chr11:69078931
|
A | T | 4 | a0006a0008a0013others(1): Show | 26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
missense_variant | MODERATE | c.1450A>T | p.Met484Leu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/25 | 1516/4969 | 1450/2259 | 484/752 | chr11 | 69078931 | ||
| chr11:69081443
|
C | T | 1 | a0021 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.1633C>T | p.Arg545Cys | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/25 | 1699/4969 | 1633/2259 | 545/752 | chr11 | 69081443 | ||
| chr11:69083946
|
T | C | 19 | a0002a0003a0004others(16): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
missense_variant&splice_region_variant | MODERATE | c.1691T>C | p.Leu564Pro | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/25 | 1757/4969 | 1691/2259 | 564/752 | chr11 | 69083946 | ||
| chr11:69085921
|
A | G | 1 | a0011 | 2 | HG02280.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.1994A>G | p.Tyr665Cys | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/25 | 2060/4969 | 1994/2259 | 665/752 | chr11 | 69085921 | ||
| chr11:69086561
|
C | T | 1 | a0007 | 8 | HG01069.hp1 HG01192.hp2 HG02083.hp2 others(5): Show |
missense_variant | MODERATE | c.2042C>T | p.Ser681Leu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/25 | 2108/4969 | 2042/2259 | 681/752 | chr11 | 69086561 | ||
| chr11:69087895
|
G | A | 4 | a0003a0009a0021others(1): Show | 71 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(68): Show |
missense_variant | MODERATE | c.2201G>A | p.Gly734Glu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2267/4969 | 2201/2259 | 734/752 | chr11 | 69087895 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:69049096
|
A | G | 4 | a0001c0005a0003c0042a0007c0009others(1): Show | 35 | HG00423.hp1 HG00639.hp1 HG01069.hp1 others(32): Show |
synonymous_variant | LOW | c.99A>G | p.Gln33Gln | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/25 | 165/4969 | 99/2259 | 33/752 | chr11 | 69049096 | ||
| chr11:69054738
|
C | T | 1 | a0004c0013 | 5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
synonymous_variant | LOW | c.192C>T | p.His64His | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/25 | 258/4969 | 192/2259 | 64/752 | chr11 | 69054738 | ||
| chr11:69055190
|
C | T | 2 | a0004c0015a0025c0040 | 4 | HG02559.hp2 HG02615.hp1 HG03540.hp1 others(1): Show |
synonymous_variant | LOW | c.267C>T | p.Thr89Thr | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/25 | 333/4969 | 267/2259 | 89/752 | chr11 | 69055190 | ||
| chr11:69055271
|
T | C | 42 | a0001c0001a0001c0005a0002c0002others(39): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
synonymous_variant | LOW | c.348T>C | p.Ala116Ala | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/25 | 414/4969 | 348/2259 | 116/752 | chr11 | 69055271 | ||
| chr11:69055298
|
C | G | 1 | a0002c0033 | 1 | HG01516.hp1 | synonymous_variant | LOW | c.375C>G | p.Thr125Thr | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/25 | 441/4969 | 375/2259 | 125/752 | chr11 | 69055298 | ||
| chr11:69057667
|
C | T | 1 | a0004c0031 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.519C>T | p.Thr173Thr | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/25 | 585/4969 | 519/2259 | 173/752 | chr11 | 69057667 | ||
| chr11:69063952
|
G | A | 3 | a0004c0015a0004c0016a0025c0040 | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
synonymous_variant | LOW | c.711G>A | p.Leu237Leu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/25 | 777/4969 | 711/2259 | 237/752 | chr11 | 69063952 | ||
| chr11:69063955
|
C | T | 1 | a0003c0020 | 2 | NA19068.hp2 NA19083.hp1 |
synonymous_variant | LOW | c.714C>T | p.Phe238Phe | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/25 | 780/4969 | 714/2259 | 238/752 | chr11 | 69063955 | ||
| chr11:69067574
|
G | A | 1 | a0004c0023 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.798G>A | p.Leu266Leu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/25 | 864/4969 | 798/2259 | 266/752 | chr11 | 69067574 | ||
| chr11:69072687
|
C | T | 1 | a0006c0030 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.1122C>T | p.Ser374Ser | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 12/25 | 1188/4969 | 1122/2259 | 374/752 | chr11 | 69072687 | ||
| chr11:69072929
|
T | C | 16 | a0002c0027a0003c0003a0003c0020others(13): Show | 138 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(135): Show |
synonymous_variant | LOW | c.1158T>C | p.Tyr386Tyr | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1224/4969 | 1158/2259 | 386/752 | chr11 | 69072929 | ||
| chr11:69072944
|
C | G | 14 | a0002c0029a0003c0003a0003c0020others(11): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
synonymous_variant | LOW | c.1173C>G | p.Leu391Leu | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/25 | 1239/4969 | 1173/2259 | 391/752 | chr11 | 69072944 | ||
| chr11:69078547
|
C | T | 1 | a0002c0019 | 2 | HG03209.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.1296C>T | p.Tyr432Tyr | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 14/25 | 1362/4969 | 1296/2259 | 432/752 | chr11 | 69078547 | ||
| chr11:69083998
|
G | T | 14 | a0003c0003a0003c0020a0003c0025others(11): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
synonymous_variant | LOW | c.1743G>T | p.Ala581Ala | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/25 | 1809/4969 | 1743/2259 | 581/752 | chr11 | 69083998 | ||
| chr11:69085889
|
C | T | 3 | a0004c0011a0004c0013a0004c0031 | 12 | HG02809.hp1 HG02886.hp2 HG02895.hp1 others(9): Show |
synonymous_variant | LOW | c.1962C>T | p.Asn654Asn | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/25 | 2028/4969 | 1962/2259 | 654/752 | chr11 | 69085889 | ||
| chr11:69086544
|
A | G | 6 | a0002c0018a0006c0007a0006c0030others(3): Show | 28 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(25): Show |
synonymous_variant | LOW | c.2025A>G | p.Val675Val | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/25 | 2091/4969 | 2025/2259 | 675/752 | chr11 | 69086544 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:69048976
|
G | A | 3 | a0004c0006t0019a0004c0006t0020a0004c0023t0019 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-22G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/25 | 22 | chr11 | 69048976 | |||||
| chr11:69087958
|
C | T | 1 | a0001c0005t0042 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 5 | chr11 | 69087958 | |||||
| chr11:69087966
|
C | T | 1 | a0002c0002t0041 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 13 | chr11 | 69087966 | |||||
| chr11:69088015
|
G | A | 29 | a0002c0002t0001a0002c0002t0023a0002c0002t0026others(26): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*62G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 62 | chr11 | 69088015 | |||||
| chr11:69088111
|
G | A | 2 | a0004c0006t0019a0004c0023t0019 | 2 | HG02145.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*158G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 158 | chr11 | 69088111 | |||||
| chr11:69088127
|
A | G | 9 | a0003c0003t0002a0003c0003t0039a0003c0020t0002others(6): Show | 72 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*174A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 174 | chr11 | 69088127 | |||||
| chr11:69088163
|
C | T | 1 | a0004c0008t0031 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*210C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 210 | chr11 | 69088163 | |||||
| chr11:69088173
|
G | A | 1 | a0002c0002t0023 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*220G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 220 | chr11 | 69088173 | |||||
| chr11:69088234
|
C | T | 1 | a0001c0001t0022 | 2 | HG02615.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*281C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 281 | chr11 | 69088234 | |||||
| chr11:69088247
|
A | G | 1 | a0002c0002t0030 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*294A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 294 | chr11 | 69088247 | |||||
| chr11:69088373
|
A | T | 3 | a0004c0011t0012a0004c0013t0015a0004c0031t0012 | 12 | HG02809.hp1 HG02886.hp2 HG02895.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*420A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 420 | chr11 | 69088373 | |||||
| chr11:69088486
|
A | G | 19 | a0002c0002t0001a0002c0002t0023a0002c0002t0026others(16): Show | 92 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*533A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 533 | chr11 | 69088486 | |||||
| chr11:69088587
|
A | G | 1 | a0002c0002t0029 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*634A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 634 | chr11 | 69088587 | |||||
| chr11:69088643
|
A | G | 3 | a0004c0008t0013a0004c0008t0031a0010c0014t0013 | 7 | HG01884.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*690A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 690 | chr11 | 69088643 | |||||
| chr11:69088756
|
G | T | 1 | a0001c0001t0011 | 7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*803G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 803 | chr11 | 69088756 | |||||
| chr11:69088804
|
C | G | 1 | a0013c0043t0025 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*851C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 851 | chr11 | 69088804 | |||||
| chr11:69089119
|
G | A | 3 | a0004c0006t0018a0005c0004t0008a0005c0004t0032 | 16 | HG00621.hp1 HG00642.hp2 HG01943.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1166G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1166 | chr11 | 69089119 | |||||
| chr11:69089139
|
G | A | 1 | a0004c0006t0033 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1186G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1186 | chr11 | 69089139 | |||||
| chr11:69089158
|
G | A | 2 | a0001c0001t0016a0011c0017t0016 | 4 | HG01934.hp1 HG02280.hp1 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1205G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1205 | chr11 | 69089158 | |||||
| chr11:69089212
|
G | A | 19 | a0002c0002t0001a0002c0002t0023a0002c0002t0026others(16): Show | 92 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*1259G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1259 | chr11 | 69089212 | |||||
| chr11:69089224
|
C | G | 1 | a0002c0002t0028 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1271C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1271 | chr11 | 69089224 | |||||
| chr11:69089242
|
TAATAAC | T | 26 | a0003c0003t0002a0003c0003t0039a0003c0020t0002others(23): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1312_*1317delACAA others(2): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1312 | INFO_REALIGN_3_PRIME | chr11 | 69089242 | ||||
| chr11:69089336
|
C | G | 19 | a0002c0002t0001a0002c0002t0023a0002c0002t0026others(16): Show | 92 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*1383C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1383 | chr11 | 69089336 | |||||
| chr11:69089375
|
T | A | 5 | a0004c0008t0013a0004c0008t0017a0004c0008t0031others(2): Show | 11 | HG01884.hp2 HG02258.hp2 HG02630.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1422T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1422 | chr11 | 69089375 | |||||
| chr11:69089382
|
G | A | 1 | a0004c0006t0036 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1429G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1429 | chr11 | 69089382 | |||||
| chr11:69089448
|
C | T | 15 | a0003c0003t0002a0003c0003t0039a0003c0020t0002others(12): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*1495C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1495 | chr11 | 69089448 | |||||
| chr11:69089457
|
G | A | 1 | a0004c0006t0036 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1504G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1504 | chr11 | 69089457 | |||||
| chr11:69089550
|
T | G | 3 | a0004c0015t0014a0004c0016t0014a0025c0040t0014 | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1597T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1597 | chr11 | 69089550 | |||||
| chr11:69089566
|
G | A | 1 | a0002c0002t0026 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1613G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1613 | chr11 | 69089566 | |||||
| chr11:69089570
|
C | T | 60 | a0002c0002t0001a0002c0002t0023a0002c0002t0026others(57): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*1617C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1617 | chr11 | 69089570 | |||||
| chr11:69089753
|
C | A | 3 | a0001c0001t0003a0017c0034t0003a0019c0032t0003 | 45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1800C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1800 | chr11 | 69089753 | |||||
| chr11:69089849
|
T | C | 1 | a0005c0004t0038 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1896T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1896 | chr11 | 69089849 | |||||
| chr11:69089889
|
G | T | 3 | a0001c0001t0003a0017c0034t0003a0019c0032t0003 | 45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1936G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1936 | chr11 | 69089889 | |||||
| chr11:69089916
|
GT | G | 25 | a0003c0003t0002a0003c0003t0039a0003c0020t0002others(22): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1971delT | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1971 | INFO_REALIGN_3_PRIME | chr11 | 69089916 | ||||
| chr11:69089942
|
C | T | 3 | a0001c0001t0003a0017c0034t0003a0019c0032t0003 | 45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1989C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 1989 | chr11 | 69089942 | |||||
| chr11:69090125
|
T | G | 1 | a0004c0006t0018 | 3 | NA19009.hp2 NA19065.hp1 NA19080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2172T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2172 | chr11 | 69090125 | |||||
| chr11:69090172
|
C | T | 1 | a0006c0007t0021 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2219C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2219 | chr11 | 69090172 | |||||
| chr11:69090194
|
TCTCATCT others(27): Show |
T | 15 | a0003c0003t0002a0003c0003t0039a0003c0020t0002others(12): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*2245_*2278delATCT others(30): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2245 | INFO_REALIGN_3_PRIME | chr11 | 69090194 | ||||
| chr11:69090222
|
C | T | 1 | a0001c0001t0035 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2269C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2269 | chr11 | 69090222 | |||||
| chr11:69090407
|
G | C | 2 | a0001c0001t0010a0001c0001t0035 | 9 | HG00558.hp2 HG00597.hp1 HG02015.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2454G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2454 | chr11 | 69090407 | |||||
| chr11:69090417
|
T | A | 1 | a0003c0003t0039 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2464T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2464 | chr11 | 69090417 | |||||
| chr11:69090422
|
T | A | 1 | a0002c0002t0027 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2469T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2469 | chr11 | 69090422 | |||||
| chr11:69090440
|
T | G | 1 | a0008c0010t0024 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2487T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2487 | chr11 | 69090440 | |||||
| chr11:69090519
|
A | G | 1 | a0004c0006t0037 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2566A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2566 | chr11 | 69090519 | |||||
| chr11:69090568
|
A | G | 4 | a0001c0001t0005a0001c0001t0010a0001c0001t0022others(1): Show | 37 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2615A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2615 | chr11 | 69090568 | |||||
| chr11:69090588
|
C | T | 1 | a0005c0004t0032 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2635C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 25/25 | 2635 | chr11 | 69090588 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:69049357
|
T | C | 277 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(274): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.109+251T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69049357 | ||||||
| chr11:69049403
|
G | A | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.109+297G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69049403 | ||||||
| chr11:69049407
|
A | G | 3 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0023t0019g0271 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+301A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69049407 | ||||||
| chr11:69049568
|
C | T | 2 | a0005c0004t0007g0268a0005c0004t0007g0269 | 2 | HG00741.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.109+462C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69049568 | ||||||
| chr11:69049582
|
C | G | 65 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(62): Show | 84 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.109+476C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69049582 | ||||||
| chr11:69049647
|
C | G | 40 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(37): Show | 44 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.109+541C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69049647 | ||||||
| chr11:69049761
|
C | T | 214 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(211): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.109+655C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69049761 | ||||||
| chr11:69049973
|
T | G | 6 | a0008c0010t0006g0025a0008c0010t0006g0100a0008c0010t0006g0101others(3): Show | 6 | HG00099.hp1 HG00323.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+867T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69049973 | ||||||
| chr11:69050256
|
C | T | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.109+1150C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050256 | ||||||
| chr11:69050429
|
G | A | 5 | a0008c0010t0006g0025a0008c0010t0006g0100a0008c0010t0006g0101others(2): Show | 5 | HG00099.hp1 HG00323.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+1323G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050429 | ||||||
| chr11:69050490
|
G | A | 3 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0023t0019g0271 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+1384G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050490 | ||||||
| chr11:69050567
|
G | A | 3 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0023t0019g0271 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+1461G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050567 | ||||||
| chr11:69050577
|
T | C | 278 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(275): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.109+1471T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050577 | ||||||
| chr11:69050629
|
C | T | 1 | a0004c0006t0036g0218 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.109+1523C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050629 | ||||||
| chr11:69050638
|
A | G | 22 | a0001c0005t0004g0001a0001c0005t0004g0008a0001c0005t0004g0023others(19): Show | 34 | HG00423.hp1 HG00639.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.109+1532A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050638 | ||||||
| chr11:69050680
|
G | A | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.109+1574G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050680 | ||||||
| chr11:69050982
|
T | C | 1 | a0004c0006t0020g0047 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.109+1876T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69050982 | ||||||
| chr11:69051025
|
G | A | 1 | a0013c0043t0025g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.109+1919G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051025 | ||||||
| chr11:69051028
|
A | G | 222 | a0001c0001t0003g0082a0001c0001t0004g0155a0001c0001t0004g0156others(219): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.109+1922A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051028 | ||||||
| chr11:69051149
|
A | G | 110 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(107): Show | 133 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.109+2043A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051149 | ||||||
| chr11:69051267
|
G | T | 219 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(216): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.109+2161G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051267 | ||||||
| chr11:69051468
|
A | G | 66 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(63): Show | 85 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.109+2362A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051468 | ||||||
| chr11:69051490
|
G | C | 12 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(9): Show | 14 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.109+2384G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051490 | ||||||
| chr11:69051543
|
C | T | 12 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(9): Show | 14 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.109+2437C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051543 | ||||||
| chr11:69051571
|
T | C | 1 | a0002c0002t0001g0220 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.110-2462T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051571 | ||||||
| chr11:69051590
|
A | C | 2 | a0003c0003t0002g0181a0003c0003t0002g0182 | 2 | NA18974.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.110-2443A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051590 | ||||||
| chr11:69051629
|
C | T | 67 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(64): Show | 86 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.110-2404C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051629 | ||||||
| chr11:69051731
|
C | T | 8 | a0001c0001t0010g0307a0001c0001t0010g0308a0001c0001t0010g0309others(5): Show | 8 | HG00558.hp2 HG02015.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.110-2302C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051731 | ||||||
| chr11:69051736
|
C | T | 21 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(18): Show | 23 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.110-2297C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051736 | ||||||
| chr11:69051819
|
A | T | 1 | a0005c0004t0008g0180 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.110-2214A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051819 | ||||||
| chr11:69051856
|
G | T | 1 | a0002c0002t0001g0267 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.110-2177G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051856 | ||||||
| chr11:69051966
|
G | A | 2 | a0004c0011t0012g0201a0004c0031t0012g0202 | 2 | HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.110-2067G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69051966 | ||||||
| chr11:69052001
|
G | A | 21 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(18): Show | 23 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.110-2032G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052001 | ||||||
| chr11:69052010
|
G | A | 1 | a0001c0001t0003g0055 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.110-2023G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052010 | ||||||
| chr11:69052030
|
G | A | 1 | a0002c0029t0001g0273 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.110-2003G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052030 | ||||||
| chr11:69052245
|
C | T | 2 | a0005c0004t0007g0037a0020c0024t0007g0179 | 3 | HG01070.hp2 HG01071.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.110-1788C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052245 | ||||||
| chr11:69052352
|
T | A | 33 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(30): Show | 37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-1681T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052352 | ||||||
| chr11:69052481
|
G | A | 2 | a0002c0027t0001g0186a0016c0036t0001g0187 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.110-1552G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052481 | ||||||
| chr11:69052560
|
A | G | 33 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(30): Show | 37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-1473A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052560 | ||||||
| chr11:69052577
|
C | T | 6 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(3): Show | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-1456C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052577 | ||||||
| chr11:69052591
|
C | T | 33 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(30): Show | 37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-1442C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052591 | ||||||
| chr11:69052600
|
T | C | 324 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(321): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.110-1433T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052600 | ||||||
| chr11:69052653
|
C | T | 21 | a0001c0001t0011g0170a0006c0007t0006g0004a0006c0007t0006g0168others(18): Show | 26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.110-1380C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052653 | ||||||
| chr11:69052655
|
G | A | 33 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(30): Show | 37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-1378G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052655 | ||||||
| chr11:69052702
|
G | A | 1 | a0012c0021t0001g0222 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.110-1331G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052702 | ||||||
| chr11:69052712
|
G | A | 1 | a0002c0002t0001g0223 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.110-1321G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052712 | ||||||
| chr11:69052788
|
T | C | 33 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(30): Show | 37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-1245T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052788 | ||||||
| chr11:69052803
|
T | A | 2 | a0004c0008t0013g0194a0004c0008t0031g0195 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.110-1230T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052803 | ||||||
| chr11:69052931
|
G | A | 1 | a0006c0030t0006g0167 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.110-1102G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052931 | ||||||
| chr11:69052948
|
C | T | 1 | a0001c0005t0004g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.110-1085C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052948 | ||||||
| chr11:69052961
|
C | T | 64 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(61): Show | 83 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.110-1072C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69052961 | ||||||
| chr11:69053014
|
C | T | 33 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(30): Show | 37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-1019C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053014 | ||||||
| chr11:69053015
|
G | A | 5 | a0004c0008t0004g0105a0004c0008t0017g0106a0004c0008t0017g0183others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-1018G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053015 | ||||||
| chr11:69053028
|
G | A | 5 | a0004c0008t0004g0105a0004c0008t0017g0106a0004c0008t0017g0183others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-1005G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053028 | ||||||
| chr11:69053049
|
T | C | 33 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(30): Show | 37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-984T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053049 | ||||||
| chr11:69053101
|
T | C | 215 | a0001c0001t0003g0082a0001c0001t0004g0155a0001c0001t0004g0156others(212): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.110-932T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053101 | ||||||
| chr11:69053148
|
C | T | 85 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(82): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.110-885C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053148 | ||||||
| chr11:69053211
|
C | T | 1 | a0001c0001t0003g0080 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.110-822C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053211 | ||||||
| chr11:69053358
|
C | G | 36 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(33): Show | 46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.110-675C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053358 | ||||||
| chr11:69053408
|
A | G | 33 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(30): Show | 37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-625A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053408 | ||||||
| chr11:69053455
|
C | T | 1 | a0004c0023t0019g0271 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.110-578C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053455 | ||||||
| chr11:69053514
|
A | G | 33 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(30): Show | 37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.110-519A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053514 | ||||||
| chr11:69053566
|
T | G | 181 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(178): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.110-467T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053566 | ||||||
| chr11:69053826
|
T | C | 2 | a0006c0007t0006g0168a0006c0007t0021g0036 | 3 | HG01106.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.110-207T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053826 | ||||||
| chr11:69053910
|
T | C | 1 | a0001c0001t0005g0274 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.110-123T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053910 | ||||||
| chr11:69053994
|
A | T | 1 | a0004c0006t0009g0217 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.110-39A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 1/24 | chr11 | 69053994 | ||||||
| chr11:69054148
|
G | A | 33 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(30): Show | 37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.174+51G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054148 | ||||||
| chr11:69054180
|
G | C | 64 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(61): Show | 83 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.174+83G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054180 | ||||||
| chr11:69054233
|
T | C | 22 | a0001c0005t0004g0001a0001c0005t0004g0008a0001c0005t0004g0023others(19): Show | 34 | HG00423.hp1 HG00639.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.174+136T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054233 | ||||||
| chr11:69054349
|
C | T | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+252C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054349 | ||||||
| chr11:69054394
|
G | A | 64 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(61): Show | 83 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.174+297G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054394 | ||||||
| chr11:69054449
|
C | T | 1 | a0001c0001t0005g0305 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.175-272C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054449 | ||||||
| chr11:69054479
|
T | C | 273 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(270): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.175-242T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054479 | ||||||
| chr11:69054545
|
C | T | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-176C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054545 | ||||||
| chr11:69054555
|
G | C | 55 | a0001c0001t0011g0170a0004c0006t0009g0016a0004c0006t0009g0190others(52): Show | 64 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.175-166G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054555 | ||||||
| chr11:69054661
|
C | T | 1 | a0004c0006t0020g0047 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.175-60C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 2/24 | chr11 | 69054661 | ||||||
| chr11:69054964
|
A | C | 2 | a0004c0008t0017g0106a0004c0008t0034g0185 | 2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.251+167A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/24 | chr11 | 69054964 | ||||||
| chr11:69055000
|
C | A | 6 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(3): Show | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.252-175C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/24 | chr11 | 69055000 | ||||||
| chr11:69055039
|
G | A | 1 | a0002c0002t0001g0226 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.252-136G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/24 | chr11 | 69055039 | ||||||
| chr11:69055077
|
G | A | 2 | a0003c0003t0002g0107a0021c0026t0002g0193 | 2 | NA18983.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.252-98G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/24 | chr11 | 69055077 | ||||||
| chr11:69055086
|
C | T | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.252-89C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 3/24 | chr11 | 69055086 | ||||||
| chr11:69055363
|
C | T | 21 | a0001c0001t0011g0170a0006c0007t0006g0004a0006c0007t0006g0168others(18): Show | 26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.429+11C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055363 | ||||||
| chr11:69055419
|
G | C | 2 | a0001c0001t0011g0170a0006c0007t0006g0169 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.429+67G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055419 | ||||||
| chr11:69055501
|
A | G | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+149A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055501 | ||||||
| chr11:69055528
|
T | TGTCAGCT others(39): Show |
126 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(123): Show | 160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.429+304_429+349dup others(46): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | 69055528 | |||||
| chr11:69055574
|
C | T | 1 | a0004c0023t0019g0271 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.429+222C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055574 | ||||||
| chr11:69055620
|
C | T | 3 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0023t0019g0271 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+268C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055620 | ||||||
| chr11:69055656
|
G | GCCAGTGT others(39): Show |
1 | a0003c0003t0002g0108 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.429+343_429+388dup others(46): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | 69055656 | |||||
| chr11:69055656
|
G | GCCAGTGT others(85): Show |
84 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(81): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.429+349_429+350ins others(92): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | 69055656 | |||||
| chr11:69055656
|
G | GCCAGTGT others(177): Show |
1 | a0003c0003t0002g0166 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.429+349_429+350ins others(184): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | 69055656 | |||||
| chr11:69055656
|
GCCAGTGT others(39): Show |
G | 12 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(9): Show | 14 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.429+343_429+388del others(46): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | 69055656 | |||||
| chr11:69055666
|
C | CGTCAGCT others(39): Show |
1 | a0001c0001t0003g0079 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.429+349_429+350ins others(46): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | 69055666 | |||||
| chr11:69055695
|
A | AACTGAGG others(85): Show |
4 | a0002c0002t0001g0221a0004c0008t0017g0106a0005c0004t0008g0081others(1): Show | 4 | HG02129.hp2 HG02630.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+349_429+350ins others(92): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | 69055695 | |||||
| chr11:69055709
|
T | G | 1 | a0005c0004t0008g0081 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.429+357T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055709 | ||||||
| chr11:69055779
|
A | G | 220 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(217): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.429+427A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055779 | ||||||
| chr11:69055965
|
C | G | 1 | a0001c0001t0003g0078 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.429+613C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055965 | ||||||
| chr11:69055975
|
C | T | 1 | a0004c0008t0031g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.429+623C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69055975 | ||||||
| chr11:69056023
|
A | G | 3 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0023t0019g0271 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+671A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056023 | ||||||
| chr11:69056076
|
G | A | 1 | a0001c0001t0003g0057 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.429+724G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056076 | ||||||
| chr11:69056176
|
C | G | 216 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(213): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.429+824C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056176 | ||||||
| chr11:69056239
|
G | A | 192 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(189): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.429+887G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056239 | ||||||
| chr11:69056275
|
G | C | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+923G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056275 | ||||||
| chr11:69056355
|
C | T | 34 | a0001c0001t0004g0290a0001c0001t0005g0011a0001c0001t0005g0048others(31): Show | 39 | HG00558.hp2 HG01496.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.429+1003C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056355 | ||||||
| chr11:69056472
|
T | C | 185 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(182): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.430-1106T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056472 | ||||||
| chr11:69056511
|
C | T | 7 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(4): Show | 7 | HG02572.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.430-1067C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056511 | ||||||
| chr11:69056588
|
C | T | 1 | a0004c0013t0015g0211 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.430-990C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056588 | ||||||
| chr11:69056636
|
T | C | 33 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(30): Show | 37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.430-942T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056636 | ||||||
| chr11:69056666
|
T | TG | 33 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(30): Show | 37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.430-910dupG | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr11 | 69056666 | |||||
| chr11:69056746
|
T | G | 1 | a0002c0019t0001g0039 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.430-832T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056746 | ||||||
| chr11:69056819
|
C | A | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-759C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056819 | ||||||
| chr11:69056886
|
A | G | 1 | a0004c0006t0036g0218 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.430-692A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056886 | ||||||
| chr11:69056919
|
C | G | 3 | a0001c0001t0005g0300a0001c0001t0005g0301a0001c0001t0005g0305 | 3 | HG03130.hp2 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.430-659C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056919 | ||||||
| chr11:69056923
|
C | T | 21 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(18): Show | 23 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.430-655C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056923 | ||||||
| chr11:69056998
|
C | T | 1 | a0009c0012t0002g0165 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.430-580C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69056998 | ||||||
| chr11:69057046
|
A | C | 218 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(215): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.430-532A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057046 | ||||||
| chr11:69057065
|
C | T | 224 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(221): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.430-513C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057065 | ||||||
| chr11:69057118
|
G | A | 1 | a0001c0001t0005g0272 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.430-460G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057118 | ||||||
| chr11:69057128
|
G | A | 12 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(9): Show | 14 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.430-450G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057128 | ||||||
| chr11:69057164
|
G | A | 33 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(30): Show | 37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.430-414G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057164 | ||||||
| chr11:69057248
|
T | C | 33 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(30): Show | 37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.430-330T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057248 | ||||||
| chr11:69057279
|
C | A | 4 | a0004c0013t0015g0038a0004c0013t0015g0208a0004c0013t0015g0209others(1): Show | 5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-299C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057279 | ||||||
| chr11:69057286
|
G | A | 4 | a0004c0013t0015g0038a0004c0013t0015g0208a0004c0013t0015g0209others(1): Show | 5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-292G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057286 | ||||||
| chr11:69057441
|
C | T | 3 | a0010c0014t0013g0198a0010c0014t0013g0199a0010c0014t0013g0200 | 3 | HG01884.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.430-137C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057441 | ||||||
| chr11:69057442
|
G | A | 41 | a0001c0001t0011g0170a0001c0005t0004g0001a0001c0005t0004g0008others(38): Show | 58 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.430-136G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057442 | ||||||
| chr11:69057501
|
G | C | 33 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(30): Show | 37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.430-77G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057501 | ||||||
| chr11:69057521
|
G | A | 4 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(1): Show | 6 | HG01346.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-57G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057521 | ||||||
| chr11:69057561
|
G | T | 18 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(15): Show | 19 | HG02572.hp2 HG02622.hp1 HG02809.hp1 others(16): Show |
intron_variant | MODIFIER | c.430-17G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057561 | ||||||
| chr11:69057569
|
A | C | 218 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(215): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.430-9A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 4/24 | chr11 | 69057569 | ||||||
| chr11:69057870
|
G | A | 33 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(30): Show | 37 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.546+176G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69057870 | ||||||
| chr11:69057924
|
G | A | 2 | a0001c0001t0022g0302a0001c0001t0022g0303 | 2 | HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.546+230G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69057924 | ||||||
| chr11:69057983
|
C | T | 17 | a0001c0005t0004g0001a0001c0005t0004g0008a0001c0005t0004g0023others(14): Show | 29 | HG00423.hp1 HG00639.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.546+289C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69057983 | ||||||
| chr11:69058007
|
C | T | 1 | a0004c0006t0033g0207 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.546+313C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058007 | ||||||
| chr11:69058030
|
C | T | 4 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(1): Show | 4 | HG02559.hp2 HG02615.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.546+336C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058030 | ||||||
| chr11:69058150
|
C | G | 1 | a0002c0002t0001g0266 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.546+456C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058150 | ||||||
| chr11:69058183
|
C | G | 280 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(277): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.546+489C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058183 | ||||||
| chr11:69058226
|
C | G | 1 | a0001c0001t0003g0055 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.546+532C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058226 | ||||||
| chr11:69058285
|
G | A | 2 | a0004c0008t0013g0194a0004c0008t0031g0195 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.546+591G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058285 | ||||||
| chr11:69058317
|
A | C | 1 | a0003c0020t0002g0164 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.546+623A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058317 | ||||||
| chr11:69058481
|
G | C | 1 | a0001c0001t0010g0307 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.546+787G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058481 | ||||||
| chr11:69058526
|
GT | G | 230 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(227): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.546+833delT | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058526 | ||||||
| chr11:69058683
|
C | T | 1 | a0002c0002t0001g0261 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.546+989C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058683 | ||||||
| chr11:69058687
|
A | G | 222 | a0001c0001t0003g0077a0001c0001t0004g0155a0001c0001t0004g0156others(219): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.546+993A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058687 | ||||||
| chr11:69058708
|
C | T | 7 | a0001c0001t0011g0299a0002c0002t0001g0017a0002c0002t0001g0275others(4): Show | 9 | HG02055.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.546+1014C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058708 | ||||||
| chr11:69058721
|
C | T | 1 | a0005c0004t0007g0162 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.546+1027C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058721 | ||||||
| chr11:69058777
|
C | A | 97 | a0001c0001t0003g0055a0001c0001t0004g0155a0001c0001t0004g0156others(94): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.546+1083C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058777 | ||||||
| chr11:69058846
|
C | T | 1 | a0004c0006t0018g0015 | 3 | NA19009.hp2 NA19065.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.546+1152C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058846 | ||||||
| chr11:69058849
|
C | T | 107 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(104): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.546+1155C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058849 | ||||||
| chr11:69058863
|
G | A | 1 | a0011c0017t0016g0285 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.546+1169G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69058863 | ||||||
| chr11:69059028
|
G | A | 3 | a0001c0001t0003g0019a0001c0001t0003g0078a0019c0032t0003g0019 | 3 | NA18956.hp2 NA18962.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.546+1334G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059028 | ||||||
| chr11:69059031
|
G | A | 1 | a0003c0003t0002g0112 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.546+1337G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059031 | ||||||
| chr11:69059063
|
C | T | 1 | a0001c0005t0004g0096 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.546+1369C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059063 | ||||||
| chr11:69059064
|
G | A | 44 | a0001c0001t0004g0290a0001c0001t0005g0011a0001c0001t0005g0048others(41): Show | 50 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.546+1370G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059064 | ||||||
| chr11:69059075
|
G | A | 97 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(94): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.546+1381G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059075 | ||||||
| chr11:69059085
|
G | C | 22 | a0001c0001t0011g0170a0006c0007t0006g0004a0006c0007t0006g0168others(19): Show | 27 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.546+1391G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059085 | ||||||
| chr11:69059101
|
G | A | 2 | a0004c0006t0019g0270a0004c0006t0020g0047 | 3 | HG02145.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.546+1407G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059101 | ||||||
| chr11:69059145
|
G | A | 1 | a0009c0012t0002g0028 | 2 | HG00544.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.546+1451G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059145 | ||||||
| chr11:69059237
|
C | A | 1 | a0004c0011t0012g0203 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.546+1543C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059237 | ||||||
| chr11:69059387
|
G | T | 27 | a0001c0001t0011g0170a0004c0015t0014g0051a0004c0015t0014g0052others(24): Show | 32 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.546+1693G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059387 | ||||||
| chr11:69059427
|
G | A | 103 | a0001c0001t0011g0170a0002c0002t0001g0002a0002c0002t0001g0003others(100): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.546+1733G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059427 | ||||||
| chr11:69059469
|
C | G | 1 | a0002c0019t0001g0039 | 2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.546+1775C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059469 | ||||||
| chr11:69059606
|
T | C | 118 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(115): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.546+1912T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059606 | ||||||
| chr11:69059614
|
G | A | 21 | a0001c0001t0011g0170a0006c0007t0006g0004a0006c0007t0006g0168others(18): Show | 26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.546+1920G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059614 | ||||||
| chr11:69059707
|
T | A | 51 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(48): Show | 65 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.546+2013T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059707 | ||||||
| chr11:69059747
|
A | C | 4 | a0004c0013t0015g0038a0004c0013t0015g0208a0004c0013t0015g0209others(1): Show | 5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+2053A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059747 | ||||||
| chr11:69059816
|
A | G | 1 | a0002c0002t0001g0260 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.546+2122A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059816 | ||||||
| chr11:69059888
|
T | C | 1 | a0003c0003t0002g0113 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.546+2194T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69059888 | ||||||
| chr11:69060113
|
A | G | 1 | a0001c0001t0005g0304 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.546+2419A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060113 | ||||||
| chr11:69060158
|
C | G | 36 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(33): Show | 46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.546+2464C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060158 | ||||||
| chr11:69060181
|
G | T | 1 | a0004c0006t0009g0190 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.546+2487G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060181 | ||||||
| chr11:69060187
|
A | G | 119 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(116): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.546+2493A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060187 | ||||||
| chr11:69060197
|
T | C | 1 | a0004c0023t0019g0271 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.546+2503T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060197 | ||||||
| chr11:69060202
|
CCA | C | 5 | a0004c0008t0004g0105a0004c0008t0017g0106a0004c0008t0017g0183others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+2513_546+2514d others(4): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr11 | 69060202 | |||||
| chr11:69060215
|
T | C | 324 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(321): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.546+2521T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060215 | ||||||
| chr11:69060249
|
T | C | 256 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(253): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.546+2555T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060249 | ||||||
| chr11:69060391
|
C | T | 16 | a0002c0002t0001g0003a0002c0002t0001g0043a0002c0002t0001g0243others(13): Show | 21 | HG00408.hp2 HG00621.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.547-2493C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060391 | ||||||
| chr11:69060692
|
G | A | 5 | a0004c0008t0004g0105a0004c0008t0017g0106a0004c0008t0017g0183others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-2192G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060692 | ||||||
| chr11:69060749
|
A | C | 1 | a0016c0036t0001g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.547-2135A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060749 | ||||||
| chr11:69060750
|
G | T | 1 | a0016c0036t0001g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.547-2134G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060750 | ||||||
| chr11:69060770
|
T | C | 117 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(114): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.547-2114T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060770 | ||||||
| chr11:69060856
|
T | C | 4 | a0001c0001t0005g0286a0001c0001t0005g0287a0001c0001t0005g0288others(1): Show | 4 | NA18612.hp1 NA18947.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-2028T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060856 | ||||||
| chr11:69060860
|
T | C | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.547-2024T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060860 | ||||||
| chr11:69060866
|
C | T | 1 | a0001c0001t0003g0076 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.547-2018C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060866 | ||||||
| chr11:69060952
|
G | A | 4 | a0004c0013t0015g0038a0004c0013t0015g0208a0004c0013t0015g0209others(1): Show | 5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-1932G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060952 | ||||||
| chr11:69060995
|
G | A | 1 | a0023c0041t0004g0088 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.547-1889G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69060995 | ||||||
| chr11:69061008
|
A | C | 4 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(1): Show | 6 | HG01346.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.547-1876A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061008 | ||||||
| chr11:69061210
|
G | A | 117 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(114): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.547-1674G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061210 | ||||||
| chr11:69061330
|
T | TC | 36 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(33): Show | 46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.547-1552dupC | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr11 | 69061330 | |||||
| chr11:69061413
|
G | A | 4 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(1): Show | 6 | HG01346.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.547-1471G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061413 | ||||||
| chr11:69061461
|
G | A | 67 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(64): Show | 88 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.547-1423G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061461 | ||||||
| chr11:69061481
|
C | T | 22 | a0001c0001t0011g0170a0006c0007t0006g0004a0006c0007t0006g0168others(19): Show | 27 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.547-1403C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061481 | ||||||
| chr11:69061580
|
C | T | 1 | a0001c0001t0005g0274 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.547-1304C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061580 | ||||||
| chr11:69061636
|
G | A | 1 | a0002c0002t0001g0254 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.547-1248G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061636 | ||||||
| chr11:69061776
|
A | T | 1 | a0013c0043t0025g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.547-1108A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061776 | ||||||
| chr11:69061854
|
GGTGGT | G | 117 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(114): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.547-1023_547-1019d others(7): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr11 | 69061854 | |||||
| chr11:69061920
|
T | C | 117 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(114): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.547-964T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69061920 | ||||||
| chr11:69062048
|
T | C | 5 | a0004c0008t0004g0105a0004c0008t0017g0106a0004c0008t0017g0183others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-836T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062048 | ||||||
| chr11:69062066
|
C | T | 117 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(114): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.547-818C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062066 | ||||||
| chr11:69062067
|
G | A | 1 | a0006c0007t0006g0171 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.547-817G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062067 | ||||||
| chr11:69062103
|
A | C | 2 | a0012c0021t0001g0222a0012c0021t0001g0253 | 2 | NA18964.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.547-781A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062103 | ||||||
| chr11:69062170
|
C | T | 96 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(93): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.547-714C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062170 | ||||||
| chr11:69062349
|
G | T | 22 | a0001c0001t0011g0170a0006c0007t0006g0004a0006c0007t0006g0168others(19): Show | 27 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.547-535G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062349 | ||||||
| chr11:69062422
|
G | A | 1 | a0009c0012t0002g0114 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.547-462G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062422 | ||||||
| chr11:69062486
|
C | T | 21 | a0001c0001t0011g0170a0006c0007t0006g0004a0006c0007t0006g0168others(18): Show | 26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.547-398C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062486 | ||||||
| chr11:69062555
|
AC | A | 36 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(33): Show | 46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.547-327delC | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr11 | 69062555 | |||||
| chr11:69062601
|
T | TTGGACA | 118 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(115): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.547-283_547-282ins others(6): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062601 | ||||||
| chr11:69062645
|
C | T | 1 | a0004c0006t0033g0207 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.547-239C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062645 | ||||||
| chr11:69062649
|
C | T | 1 | a0002c0002t0001g0252 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.547-235C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062649 | ||||||
| chr11:69062758
|
G | A | 118 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(115): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.547-126G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062758 | ||||||
| chr11:69062805
|
C | T | 5 | a0004c0008t0004g0105a0004c0008t0017g0106a0004c0008t0017g0183others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-79C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 5/24 | chr11 | 69062805 | ||||||
| chr11:69063044
|
C | T | 1 | a0003c0003t0002g0108 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.653+54C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063044 | ||||||
| chr11:69063160
|
T | G | 192 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(189): Show | 245 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.653+170T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063160 | ||||||
| chr11:69063197
|
T | C | 3 | a0010c0014t0013g0198a0010c0014t0013g0199a0010c0014t0013g0200 | 3 | HG01884.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.653+207T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063197 | ||||||
| chr11:69063222
|
C | T | 1 | a0010c0014t0013g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.653+232C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063222 | ||||||
| chr11:69063239
|
G | A | 77 | a0002c0002t0001g0229a0002c0002t0001g0265a0003c0003t0002g0009others(74): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.653+249G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063239 | ||||||
| chr11:69063260
|
G | C | 9 | a0001c0001t0011g0170a0001c0001t0011g0291a0001c0001t0011g0298others(6): Show | 9 | HG02451.hp1 HG02615.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.653+270G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063260 | ||||||
| chr11:69063260
|
G | GC | 6 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(3): Show | 6 | HG02559.hp2 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.653+271dupC | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr11 | 69063260 | |||||
| chr11:69063290
|
C | T | 1 | a0005c0004t0007g0162 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.653+300C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063290 | ||||||
| chr11:69063323
|
C | T | 5 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0016t0014g0049others(2): Show | 5 | HG02451.hp1 HG02615.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+333C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063323 | ||||||
| chr11:69063383
|
T | C | 324 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(321): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.653+393T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063383 | ||||||
| chr11:69063390
|
C | T | 3 | a0004c0008t0017g0106a0004c0008t0017g0184a0004c0008t0034g0185 | 3 | HG02630.hp1 HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.653+400C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063390 | ||||||
| chr11:69063456
|
G | A | 31 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(28): Show | 40 | HG00408.hp1 HG00438.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.654-439G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063456 | ||||||
| chr11:69063467
|
A | G | 1 | a0001c0001t0010g0314 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.654-428A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063467 | ||||||
| chr11:69063501
|
G | A | 2 | a0002c0002t0001g0189a0002c0002t0001g0255 | 2 | HG00140.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.654-394G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063501 | ||||||
| chr11:69063514
|
C | T | 1 | a0002c0027t0001g0186 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.654-381C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063514 | ||||||
| chr11:69063698
|
C | G | 147 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(144): Show | 183 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.654-197C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063698 | ||||||
| chr11:69063699
|
G | A | 2 | a0002c0027t0001g0186a0016c0036t0001g0187 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.654-196G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063699 | ||||||
| chr11:69063755
|
G | A | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.654-140G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063755 | ||||||
| chr11:69063825
|
C | G | 90 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(87): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.654-70C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063825 | ||||||
| chr11:69063828
|
G | A | 1 | a0001c0001t0003g0058 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.654-67G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 6/24 | chr11 | 69063828 | ||||||
| chr11:69063997
|
T | C | 1 | a0001c0001t0022g0302 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.726+30T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69063997 | ||||||
| chr11:69064068
|
C | T | 1 | a0001c0001t0003g0021 | 2 | NA18986.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.726+101C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064068 | ||||||
| chr11:69064175
|
G | A | 1 | a0006c0007t0021g0036 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.726+208G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064175 | ||||||
| chr11:69064285
|
C | CT | 111 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(108): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.726+318_726+319ins others(1): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064285 | ||||||
| chr11:69064317
|
C | T | 4 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(1): Show | 6 | HG01346.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.726+350C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064317 | ||||||
| chr11:69064431
|
C | T | 36 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(33): Show | 46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.726+464C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064431 | ||||||
| chr11:69064441
|
C | T | 279 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(276): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.726+474C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064441 | ||||||
| chr11:69064452
|
C | T | 111 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(108): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.726+485C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064452 | ||||||
| chr11:69064562
|
A | C | 111 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(108): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.726+595A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064562 | ||||||
| chr11:69064663
|
A | C | 1 | a0002c0002t0001g0042 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.726+696A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064663 | ||||||
| chr11:69064753
|
G | A | 23 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(20): Show | 35 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.726+786G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064753 | ||||||
| chr11:69064883
|
T | TTGTC | 21 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(18): Show | 23 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.726+919_726+920ins others(4): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | 69064883 | |||||
| chr11:69064929
|
CTG | C | 84 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(81): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.726+972_726+973del others(2): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | 69064929 | |||||
| chr11:69064945
|
A | T | 1 | a0005c0004t0038g0139 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.726+978A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064945 | ||||||
| chr11:69064959
|
AGTGTCTG others(33): Show |
A | 1 | a0003c0003t0002g0108 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.726+1002_726+1041d others(42): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | 69064959 | |||||
| chr11:69064964
|
C | CTG | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.726+1000_726+1001d others(4): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | 69064964 | |||||
| chr11:69064981
|
A | G | 68 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(65): Show | 89 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.726+1014A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69064981 | ||||||
| chr11:69064981
|
ATGTC | A | 21 | a0006c0007t0006g0004a0006c0007t0006g0168a0006c0007t0006g0169others(18): Show | 26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.726+1018_726+1021d others(6): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | 69064981 | |||||
| chr11:69065020
|
T | G | 3 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0023t0019g0271 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.726+1053T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065020 | ||||||
| chr11:69065034
|
T | C | 1 | a0003c0003t0002g0108 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.726+1067T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065034 | ||||||
| chr11:69065037
|
G | A | 93 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(90): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.726+1070G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065037 | ||||||
| chr11:69065062
|
CTA | C | 178 | a0001c0001t0003g0082a0001c0001t0004g0155a0001c0001t0004g0156others(175): Show | 230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.726+1097_726+1098d others(4): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | 69065062 | |||||
| chr11:69065062
|
CTATG | C | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.726+1097_726+1100d others(6): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr11 | 69065062 | |||||
| chr11:69065126
|
G | A | 1 | a0005c0004t0008g0140 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.726+1159G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065126 | ||||||
| chr11:69065155
|
T | C | 1 | a0001c0001t0005g0292 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.726+1188T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065155 | ||||||
| chr11:69065236
|
C | T | 1 | a0004c0006t0033g0207 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.726+1269C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065236 | ||||||
| chr11:69065247
|
G | A | 1 | a0001c0001t0004g0290 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.726+1280G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065247 | ||||||
| chr11:69065262
|
C | G | 111 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(108): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.726+1295C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065262 | ||||||
| chr11:69065366
|
A | G | 279 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(276): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.726+1399A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065366 | ||||||
| chr11:69065380
|
G | A | 70 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(67): Show | 91 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.726+1413G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065380 | ||||||
| chr11:69065419
|
C | T | 1 | a0003c0003t0002g0152 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.726+1452C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065419 | ||||||
| chr11:69065507
|
G | A | 2 | a0001c0005t0042g0089a0023c0041t0004g0088 | 2 | HG00639.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.726+1540G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065507 | ||||||
| chr11:69065605
|
C | G | 279 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(276): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.726+1638C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065605 | ||||||
| chr11:69065925
|
G | C | 2 | a0001c0005t0004g0023a0001c0005t0004g0085 | 3 | NA18950.hp1 NA18975.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.727-1578G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065925 | ||||||
| chr11:69065953
|
G | T | 1 | a0002c0002t0001g0264 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.727-1550G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065953 | ||||||
| chr11:69065988
|
G | C | 1 | a0001c0001t0005g0277 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.727-1515G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065988 | ||||||
| chr11:69065994
|
C | T | 111 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(108): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.727-1509C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69065994 | ||||||
| chr11:69066027
|
T | A | 1 | a0003c0020t0002g0164 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.727-1476T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066027 | ||||||
| chr11:69066028
|
G | T | 1 | a0003c0020t0002g0164 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.727-1475G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066028 | ||||||
| chr11:69066045
|
C | T | 1 | a0002c0002t0028g0251 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.727-1458C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066045 | ||||||
| chr11:69066053
|
A | G | 279 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(276): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.727-1450A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066053 | ||||||
| chr11:69066069
|
T | A | 1 | a0001c0001t0003g0055 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.727-1434T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066069 | ||||||
| chr11:69066097
|
T | C | 1 | a0001c0001t0003g0059 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.727-1406T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066097 | ||||||
| chr11:69066127
|
A | G | 111 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(108): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.727-1376A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066127 | ||||||
| chr11:69066140
|
T | C | 2 | a0001c0001t0011g0293a0001c0001t0011g0294 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.727-1363T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066140 | ||||||
| chr11:69066164
|
A | G | 111 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(108): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.727-1339A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066164 | ||||||
| chr11:69066213
|
C | T | 4 | a0001c0001t0003g0019a0001c0001t0003g0072a0001c0001t0003g0078others(1): Show | 4 | NA18956.hp2 NA18962.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.727-1290C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066213 | ||||||
| chr11:69066235
|
G | C | 111 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(108): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.727-1268G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066235 | ||||||
| chr11:69066258
|
T | C | 274 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(271): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.727-1245T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066258 | ||||||
| chr11:69066327
|
A | T | 24 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(21): Show | 36 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.727-1176A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066327 | ||||||
| chr11:69066380
|
C | T | 1 | a0006c0007t0006g0178 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.727-1123C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066380 | ||||||
| chr11:69066415
|
A | G | 157 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(154): Show | 205 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.727-1088A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066415 | ||||||
| chr11:69066490
|
T | C | 1 | a0002c0002t0001g0256 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.727-1013T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066490 | ||||||
| chr11:69066568
|
C | A | 4 | a0003c0003t0002g0009a0003c0003t0002g0112a0003c0003t0002g0117others(1): Show | 7 | HG00733.hp1 HG01255.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-935C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066568 | ||||||
| chr11:69066636
|
C | T | 111 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(108): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.727-867C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066636 | ||||||
| chr11:69066643
|
G | T | 1 | a0004c0023t0019g0271 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.727-860G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066643 | ||||||
| chr11:69066648
|
G | C | 1 | a0004c0011t0012g0204 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.727-855G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066648 | ||||||
| chr11:69066713
|
G | C | 6 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(3): Show | 6 | HG00544.hp2 HG01928.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.727-790G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066713 | ||||||
| chr11:69066771
|
C | T | 1 | a0013c0043t0025g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.727-732C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066771 | ||||||
| chr11:69066799
|
G | T | 1 | a0001c0001t0003g0071 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.727-704G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066799 | ||||||
| chr11:69066873
|
A | G | 111 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(108): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.727-630A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066873 | ||||||
| chr11:69066905
|
G | A | 132 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(129): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.727-598G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066905 | ||||||
| chr11:69066923
|
C | G | 1 | a0001c0001t0011g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.727-580C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066923 | ||||||
| chr11:69066961
|
C | T | 1 | a0004c0006t0020g0047 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.727-542C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69066961 | ||||||
| chr11:69067039
|
A | G | 4 | a0002c0002t0001g0017a0002c0002t0001g0275a0002c0002t0001g0276others(1): Show | 6 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.727-464A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69067039 | ||||||
| chr11:69067112
|
C | A | 3 | a0001c0001t0005g0011a0001c0001t0005g0295a0001c0001t0005g0296 | 6 | NA18942.hp1 NA18945.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.727-391C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69067112 | ||||||
| chr11:69067176
|
A | G | 1 | a0002c0002t0001g0220 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.727-327A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69067176 | ||||||
| chr11:69067205
|
C | T | 4 | a0001c0001t0010g0284a0001c0001t0010g0307a0001c0001t0010g0312others(1): Show | 4 | HG00597.hp1 NA18747.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.727-298C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69067205 | ||||||
| chr11:69067363
|
G | A | 70 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(67): Show | 91 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.727-140G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69067363 | ||||||
| chr11:69067500
|
T | C | 279 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(276): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
splice_region_variant&intron_variant | LOW | c.727-3T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 7/24 | chr11 | 69067500 | ||||||
| chr11:69067714
|
T | A | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.829+109T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69067714 | ||||||
| chr11:69067845
|
T | G | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.829+240T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69067845 | ||||||
| chr11:69067904
|
A | T | 243 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(240): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.829+299A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69067904 | ||||||
| chr11:69068017
|
G | T | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.829+412G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068017 | ||||||
| chr11:69068132
|
G | T | 1 | a0004c0008t0013g0197 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.829+527G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068132 | ||||||
| chr11:69068159
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.829+554C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068159 | ||||||
| chr11:69068160
|
G | A | 12 | a0004c0008t0004g0105a0004c0008t0013g0194a0004c0008t0013g0196others(9): Show | 12 | HG01884.hp2 HG02258.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.829+555G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068160 | ||||||
| chr11:69068289
|
A | C | 1 | a0009c0012t0002g0028 | 2 | HG00544.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.829+684A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068289 | ||||||
| chr11:69068303
|
C | G | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.829+698C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068303 | ||||||
| chr11:69068314
|
G | GCCGTCTG others(71): Show |
1 | a0004c0016t0014g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.829+736_829+737ins others(78): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068314 | |||||
| chr11:69068316
|
CGTCTGAG others(734): Show |
C | 1 | a0001c0001t0011g0298 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.829+734_830-1351de others(1): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068316 | |||||
| chr11:69068329
|
G | GGAAGTGA others(32): Show |
2 | a0005c0004t0007g0111a0005c0004t0007g0141 | 2 | HG01168.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.829+736_829+737ins others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068329 | |||||
| chr11:69068342
|
C | CTGGGAGC others(1045): Show |
3 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157 | 3 | HG00438.hp2 NA18945.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.829+853_829+854ins others(1052): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068342 | |||||
| chr11:69068342
|
C | CTGGGAGC others(149): Show |
1 | a0001c0001t0003g0075 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.829+771_829+772ins others(156): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068342 | |||||
| chr11:69068342
|
C | G | 119 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(116): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.829+737C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068342 | ||||||
| chr11:69068353
|
A | G | 2 | a0004c0006t0019g0270a0004c0006t0020g0047 | 3 | HG02145.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.829+748A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068353 | ||||||
| chr11:69068354
|
C | T | 1 | a0010c0014t0013g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.829+749C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068354 | ||||||
| chr11:69068364
|
C | T | 12 | a0004c0008t0004g0105a0004c0008t0013g0194a0004c0008t0013g0196others(9): Show | 12 | HG01884.hp2 HG02258.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.829+759C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068364 | ||||||
| chr11:69068368
|
G | T | 82 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(79): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.829+763G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068368 | ||||||
| chr11:69068381
|
G | C | 9 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0015t0014g0051others(6): Show | 10 | HG01168.hp2 HG02080.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.829+776G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068381 | ||||||
| chr11:69068381
|
G | GTGGGAGC others(32): Show |
4 | a0001c0001t0010g0311a0004c0006t0009g0016a0004c0006t0009g0190others(1): Show | 6 | HG00558.hp2 HG01346.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.829+815_829+853dup others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068381 | |||||
| chr11:69068381
|
GTGGGAGC others(32): Show |
G | 1 | a0002c0002t0001g0189 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.829+815_829+853del others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068381 | |||||
| chr11:69068420
|
C | CTGGGAGC others(188): Show |
4 | a0004c0013t0015g0038a0004c0013t0015g0208a0004c0013t0015g0209others(1): Show | 5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.829+853_829+854ins others(195): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068420 | |||||
| chr11:69068420
|
C | CTGGGAGC others(227): Show |
2 | a0004c0011t0012g0205a0004c0011t0012g0210 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.829+853_829+854ins others(234): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068420 | |||||
| chr11:69068420
|
C | G | 1 | a0001c0001t0003g0075 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.829+815C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068420 | ||||||
| chr11:69068420
|
CTGGGAGC others(32): Show |
C | 61 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(58): Show | 80 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.829+893_829+931del others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068420 | |||||
| chr11:69068434
|
G | GTCTGAGT others(32): Show |
1 | a0003c0003t0002g0119 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.829+853_829+854ins others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068434 | |||||
| chr11:69068456
|
G | C | 34 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(31): Show | 44 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.829+851G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068456 | ||||||
| chr11:69068459
|
G | C | 210 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(207): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.829+854G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068459 | ||||||
| chr11:69068473
|
G | A | 1 | a0003c0003t0002g0013 | 3 | HG01243.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.829+868G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068473 | ||||||
| chr11:69068498
|
G | C | 15 | a0002c0002t0001g0042a0002c0002t0001g0043a0002c0002t0001g0230others(12): Show | 17 | HG00741.hp2 HG01074.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.829+893G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068498 | ||||||
| chr11:69068498
|
G | GTGGGAGC others(188): Show |
7 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(4): Show | 7 | HG02572.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.829+931_829+932ins others(195): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068498 | |||||
| chr11:69068537
|
C | CTGGGAGC others(32): Show |
74 | a0003c0003t0002g0009a0003c0003t0002g0014a0003c0003t0002g0027others(71): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.829+1016_829+1054d others(41): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068537 | |||||
| chr11:69068537
|
C | G | 78 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(75): Show | 94 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.829+932C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068537 | ||||||
| chr11:69068538
|
T | TGGGAGCA others(110): Show |
1 | a0004c0016t0014g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.829+1005_829+1006i others(119): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068538 | |||||
| chr11:69068548
|
A | G | 6 | a0002c0002t0001g0043a0002c0002t0001g0230a0002c0002t0001g0243others(3): Show | 7 | HG01192.hp1 NA18956.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.829+943A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068548 | ||||||
| chr11:69068576
|
G | C | 4 | a0001c0001t0010g0284a0001c0001t0010g0307a0001c0001t0010g0312others(1): Show | 4 | HG00597.hp1 NA18747.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.829+971G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068576 | ||||||
| chr11:69068577
|
T | TGGGAGCA others(149): Show |
4 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(1): Show | 4 | HG02559.hp2 HG02615.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.829+1022_829+1023i others(158): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068577 | |||||
| chr11:69068587
|
A | G | 60 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(57): Show | 78 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.829+982A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068587 | ||||||
| chr11:69068611
|
C | G | 1 | a0001c0005t0004g0095 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.829+1006C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068611 | ||||||
| chr11:69068615
|
G | GTGGGAGC others(691): Show |
1 | a0003c0003t0002g0034 | 2 | HG01346.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.829+1054_829+1055i others(700): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068615 | |||||
| chr11:69068621
|
GCAGGACC others(32): Show |
G | 1 | a0002c0002t0001g0042 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.829+1055_829+1093d others(41): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068621 | |||||
| chr11:69068629
|
G | A | 4 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(1): Show | 4 | HG02559.hp2 HG02615.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.829+1024G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068629 | ||||||
| chr11:69068629
|
G | GTCTGAGT others(149): Show |
1 | a0004c0016t0014g0049 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.829+1054_829+1055i others(158): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068629 | |||||
| chr11:69068651
|
G | A | 1 | a0001c0005t0004g0095 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.829+1046G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068651 | ||||||
| chr11:69068654
|
G | C | 7 | a0002c0002t0001g0043a0002c0002t0001g0230a0002c0002t0001g0243others(4): Show | 8 | HG01192.hp1 HG03579.hp1 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.829+1049G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068654 | ||||||
| chr11:69068655
|
T | G | 1 | a0001c0005t0004g0095 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.829+1050T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068655 | ||||||
| chr11:69068660
|
A | G | 279 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(276): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.829+1055A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068660 | ||||||
| chr11:69068686
|
G | GACCGCAG others(227): Show |
1 | a0002c0002t0001g0230 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.829+1123_829+1124i others(236): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068686 | |||||
| chr11:69068693
|
G | C | 63 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(60): Show | 83 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.829+1088G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068693 | ||||||
| chr11:69068694
|
TGGGAGCA others(71): Show |
T | 1 | a0001c0005t0004g0095 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.829+1163_829+1240d others(80): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068694 | |||||
| chr11:69068725
|
G | T | 5 | a0002c0002t0001g0017a0002c0002t0001g0275a0002c0002t0001g0276others(2): Show | 7 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.829+1120G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068725 | ||||||
| chr11:69068728
|
C | CGCAGTGG others(32): Show |
4 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(1): Show | 4 | HG02559.hp2 HG02615.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.829+1161_829+1162i others(41): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068728 | |||||
| chr11:69068728
|
C | G | 23 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(20): Show | 35 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.829+1123C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068728 | ||||||
| chr11:69068729
|
G | A | 6 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(3): Show | 7 | HG01192.hp1 HG03579.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.829+1124G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068729 | ||||||
| chr11:69068733
|
T | G | 6 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(3): Show | 7 | HG01192.hp1 HG03579.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.829+1128T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068733 | ||||||
| chr11:69068768
|
A | G | 26 | a0001c0005t0004g0056a0002c0002t0001g0043a0002c0002t0001g0243others(23): Show | 30 | HG00323.hp2 HG01192.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.829+1163A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068768 | ||||||
| chr11:69068772
|
G | T | 24 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(21): Show | 28 | HG00323.hp2 HG01192.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.829+1167G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068772 | ||||||
| chr11:69068785
|
G | A | 7 | a0001c0005t0004g0095a0002c0002t0001g0043a0002c0002t0001g0243others(4): Show | 8 | HG01192.hp1 HG02257.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.829+1180G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068785 | ||||||
| chr11:69068807
|
G | A | 8 | a0003c0003t0002g0013a0003c0003t0002g0134a0003c0003t0002g0137others(5): Show | 10 | HG00323.hp2 HG01243.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.829+1202G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068807 | ||||||
| chr11:69068810
|
G | C | 1 | a0022c0028t0040g0242 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.829+1205G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068810 | ||||||
| chr11:69068811
|
T | G | 8 | a0003c0003t0002g0013a0003c0003t0002g0134a0003c0003t0002g0137others(5): Show | 10 | HG00323.hp2 HG01243.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.829+1206T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068811 | ||||||
| chr11:69068821
|
ACCGTCTG others(538): Show |
A | 1 | a0022c0028t0040g0242 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.829+1244_830-1037d others(2): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068821 | |||||
| chr11:69068823
|
C | T | 56 | a0001c0001t0004g0290a0003c0003t0002g0009a0003c0003t0002g0014others(53): Show | 68 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.829+1218C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068823 | ||||||
| chr11:69068824
|
G | A | 153 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(150): Show | 200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.829+1219G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068824 | ||||||
| chr11:69068849
|
C | G | 234 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(231): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.829+1244C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068849 | ||||||
| chr11:69068862
|
C | T | 4 | a0003c0003t0002g0013a0003c0003t0002g0134a0003c0003t0002g0137others(1): Show | 6 | HG00323.hp2 HG01243.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.829+1257C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068862 | ||||||
| chr11:69068885
|
GCACTGGG others(304): Show |
G | 2 | a0003c0003t0002g0013a0004c0006t0009g0192 | 4 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.829+1283_830-1232d others(2): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068885 | |||||
| chr11:69068888
|
C | G | 152 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(149): Show | 186 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.829+1283C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068888 | ||||||
| chr11:69068889
|
T | TGGGAGCA others(31): Show |
2 | a0005c0004t0008g0081a0005c0004t0008g0151 | 2 | HG02129.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.829+1309_829+1310i others(40): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068889 | |||||
| chr11:69068920
|
G | T | 7 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(4): Show | 8 | HG01192.hp1 HG02257.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.829+1315G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068920 | ||||||
| chr11:69068923
|
C | A | 84 | a0003c0003t0002g0009a0003c0003t0002g0014a0003c0003t0002g0027others(81): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.829+1318C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068923 | ||||||
| chr11:69068927
|
C | G | 42 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(39): Show | 56 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.829+1322C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068927 | ||||||
| chr11:69068940
|
CGTCTGAG others(32): Show |
C | 1 | a0001c0005t0004g0095 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.829+1354_829+1392d others(41): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69068940 | |||||
| chr11:69068959
|
T | G | 151 | a0001c0001t0003g0060a0001c0001t0004g0155a0001c0001t0004g0156others(148): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.829+1354T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068959 | ||||||
| chr11:69068962
|
C | A | 3 | a0003c0003t0002g0134a0003c0003t0002g0137a0003c0003t0002g0160 | 3 | HG00323.hp2 HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.829+1357C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068962 | ||||||
| chr11:69068966
|
C | G | 272 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(269): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.829+1361C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068966 | ||||||
| chr11:69068979
|
T | C | 181 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(178): Show | 230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.829+1374T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69068979 | ||||||
| chr11:69069002
|
G | A | 1 | a0004c0011t0012g0203 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.829+1397G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069002 | ||||||
| chr11:69069006
|
T | G | 5 | a0004c0011t0012g0201a0004c0011t0012g0203a0004c0011t0012g0204others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.829+1401T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069006 | ||||||
| chr11:69069018
|
T | C | 30 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0008t0017g0106others(27): Show | 36 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.830-1412T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069018 | ||||||
| chr11:69069019
|
GTCTGAGT others(71): Show |
G | 1 | a0004c0008t0017g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.830-1350_830-1273d others(80): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069019 | |||||
| chr11:69069041
|
G | A | 9 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(6): Show | 10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1389G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069041 | ||||||
| chr11:69069045
|
T | G | 9 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(6): Show | 10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1385T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069045 | ||||||
| chr11:69069057
|
T | C | 8 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0011t0012g0201others(5): Show | 9 | HG02145.hp1 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.830-1373T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069057 | ||||||
| chr11:69069058
|
G | A | 9 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(6): Show | 10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1372G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069058 | ||||||
| chr11:69069058
|
G | C | 97 | a0003c0003t0002g0009a0003c0003t0002g0014a0003c0003t0002g0027others(94): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.830-1372G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069058 | ||||||
| chr11:69069076
|
GACC | G | 90 | a0003c0003t0002g0009a0003c0003t0002g0014a0003c0003t0002g0027others(87): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.830-1351_830-1349d others(5): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069076 | |||||
| chr11:69069078
|
C | CACGGGGA others(1232): Show |
1 | a0004c0006t0009g0213 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.830-1352_830-1351i others(1241): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069078 | ||||||
| chr11:69069078
|
C | CACGGGGA others(299): Show |
1 | a0004c0006t0033g0207 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.830-1352_830-1351i others(308): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069078 | ||||||
| chr11:69069078
|
C | CACGGGGA others(1312): Show |
1 | a0004c0006t0009g0217 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.830-1352_830-1351i others(1321): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069078 | ||||||
| chr11:69069078
|
C | CACGGGGA others(1234): Show |
1 | a0004c0006t0009g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.830-1352_830-1351i others(1243): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069078 | ||||||
| chr11:69069078
|
C | CACGGGGA others(1273): Show |
1 | a0004c0006t0009g0215 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.830-1352_830-1351i others(1282): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069078 | ||||||
| chr11:69069078
|
C | CACGGGGA others(1234): Show |
1 | a0014c0038t0009g0212 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.830-1352_830-1351i others(1243): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069078 | ||||||
| chr11:69069078
|
C | CACGGGGA others(1234): Show |
1 | a0004c0006t0009g0216 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.830-1352_830-1351i others(1243): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069078 | ||||||
| chr11:69069079
|
C | CGCACTGG others(146): Show |
2 | a0004c0006t0019g0270a0004c0006t0020g0047 | 3 | HG02145.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.830-1351_830-1350i others(155): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069079 | ||||||
| chr11:69069079
|
C | CGCAGTGG others(185): Show |
1 | a0004c0023t0019g0271 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.830-1351_830-1350i others(194): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069079 | ||||||
| chr11:69069079
|
C | CGCAGTGG others(223): Show |
5 | a0004c0011t0012g0201a0004c0011t0012g0203a0004c0011t0012g0204others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.830-1351_830-1350i others(232): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069079 | ||||||
| chr11:69069079
|
C | CGCAGTGG others(29): Show |
1 | a0003c0003t0002g0134 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.830-1351_830-1350i others(38): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069079 | ||||||
| chr11:69069079
|
C | G | 7 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(4): Show | 7 | HG02572.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.830-1351C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069079 | ||||||
| chr11:69069080
|
A | G | 11 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(8): Show | 12 | HG01192.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.830-1350A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069080 | ||||||
| chr11:69069083
|
G | C | 106 | a0003c0003t0002g0009a0003c0003t0002g0014a0003c0003t0002g0027others(103): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.830-1347G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069083 | ||||||
| chr11:69069084
|
G | T | 11 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(8): Show | 12 | HG01192.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.830-1346G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069084 | ||||||
| chr11:69069097
|
A | C | 2 | a0003c0003t0002g0137a0003c0003t0002g0160 | 2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.830-1333A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069097 | ||||||
| chr11:69069097
|
A | G | 9 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(6): Show | 10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1333A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069097 | ||||||
| chr11:69069097
|
ATCTGAGT others(538): Show |
A | 1 | a0011c0017t0016g0285 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.830-1295_830-751de others(1): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069097 | |||||
| chr11:69069122
|
G | C | 2 | a0003c0003t0002g0137a0003c0003t0002g0160 | 2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.830-1308G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069122 | ||||||
| chr11:69069123
|
T | G | 2 | a0003c0003t0002g0137a0003c0003t0002g0160 | 2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.830-1307T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069123 | ||||||
| chr11:69069135
|
T | C | 1 | a0004c0008t0017g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.830-1295T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069135 | ||||||
| chr11:69069135
|
TGTCTGAG others(70): Show |
T | 2 | a0001c0001t0011g0293a0001c0001t0011g0294 | 2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.830-1256_830-1180d others(79): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069135 | |||||
| chr11:69069136
|
G | A | 2 | a0003c0003t0002g0137a0003c0003t0002g0160 | 2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.830-1294G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069136 | ||||||
| chr11:69069149
|
G | C | 9 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(6): Show | 10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1281G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069149 | ||||||
| chr11:69069154
|
G | T | 2 | a0003c0003t0002g0137a0003c0003t0002g0160 | 2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.830-1276G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069154 | ||||||
| chr11:69069155
|
AC | A | 9 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(6): Show | 10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1273delC | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069155 | |||||
| chr11:69069157
|
C | T | 1 | a0004c0006t0007g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.830-1273C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069157 | ||||||
| chr11:69069158
|
G | A | 9 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(6): Show | 10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1272G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069158 | ||||||
| chr11:69069162
|
T | G | 9 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(6): Show | 10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1268T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069162 | ||||||
| chr11:69069174
|
T | C | 117 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(114): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.830-1256T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069174 | ||||||
| chr11:69069174
|
TGTCTGAG others(265): Show |
T | 2 | a0003c0003t0002g0137a0003c0003t0002g0160 | 2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.830-1242_830-971de others(1): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069174 | |||||
| chr11:69069188
|
C | G | 9 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(6): Show | 10 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1242C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069188 | ||||||
| chr11:69069194
|
A | AC | 13 | a0001c0001t0005g0300a0001c0001t0005g0301a0001c0001t0005g0305others(10): Show | 14 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.830-1235dupC | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069194 | |||||
| chr11:69069196
|
A | G | 13 | a0001c0001t0005g0300a0001c0001t0005g0301a0001c0001t0005g0305others(10): Show | 14 | HG01192.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.830-1234A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069196 | ||||||
| chr11:69069200
|
G | T | 12 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(9): Show | 15 | HG01192.hp1 HG01243.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.830-1230G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069200 | ||||||
| chr11:69069200
|
GGGGAGCA others(305): Show |
G | 1 | a0004c0008t0017g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.830-1192_830-881de others(1): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069200 | |||||
| chr11:69069210
|
A | G | 1 | a0005c0004t0007g0037 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.830-1220A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069210 | ||||||
| chr11:69069234
|
C | T | 1 | a0006c0007t0006g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.830-1196C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069234 | ||||||
| chr11:69069238
|
G | A | 1 | a0006c0007t0006g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.830-1192G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069238 | ||||||
| chr11:69069238
|
G | C | 9 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(6): Show | 10 | HG01168.hp2 HG01192.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.830-1192G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069238 | ||||||
| chr11:69069251
|
C | T | 4 | a0002c0002t0001g0248a0002c0002t0001g0249a0002c0002t0001g0250others(1): Show | 4 | NA18941.hp2 NA18979.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.830-1179C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069251 | ||||||
| chr11:69069265
|
G | T | 21 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(18): Show | 23 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.830-1165G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069265 | ||||||
| chr11:69069270
|
G | C | 11 | a0004c0011t0012g0201a0004c0011t0012g0203a0004c0011t0012g0204others(8): Show | 12 | HG02809.hp1 HG02886.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.830-1160G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069270 | ||||||
| chr11:69069273
|
C | A | 1 | a0003c0003t0002g0013 | 3 | HG01243.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.830-1157C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069273 | ||||||
| chr11:69069277
|
C | CTGGGAGC others(32): Show |
1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.830-1139_830-1101d others(41): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069277 | |||||
| chr11:69069277
|
C | G | 33 | a0001c0001t0003g0060a0002c0002t0001g0017a0002c0002t0001g0275others(30): Show | 42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.830-1153C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069277 | ||||||
| chr11:69069288
|
A | G | 1 | a0006c0007t0006g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.830-1142A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069288 | ||||||
| chr11:69069290
|
C | T | 1 | a0016c0036t0001g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.830-1140C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069290 | ||||||
| chr11:69069309
|
G | T | 8 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(5): Show | 9 | HG01192.hp1 HG02258.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.830-1121G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069309 | ||||||
| chr11:69069320
|
G | A | 1 | a0003c0003t0002g0013 | 3 | HG01243.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.830-1110G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069320 | ||||||
| chr11:69069327
|
A | G | 5 | a0004c0008t0004g0105a0004c0008t0017g0183a0006c0007t0006g0169others(2): Show | 5 | HG02257.hp2 HG02258.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.830-1103A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069327 | ||||||
| chr11:69069327
|
ACCATCTG others(32): Show |
A | 1 | a0003c0003t0002g0013 | 3 | HG01243.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.830-1100_830-1062d others(41): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069327 | |||||
| chr11:69069329
|
C | T | 1 | a0002c0027t0001g0186 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.830-1101C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069329 | ||||||
| chr11:69069330
|
A | G | 273 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(270): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.830-1100A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069330 | ||||||
| chr11:69069348
|
T | G | 135 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(132): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.830-1082T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069348 | ||||||
| chr11:69069355
|
G | C | 20 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(17): Show | 22 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(19): Show |
intron_variant | MODIFIER | c.830-1075G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069355 | ||||||
| chr11:69069366
|
G | A | 115 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(112): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.830-1064G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069366 | ||||||
| chr11:69069366
|
G | GCCGTCTG others(71): Show |
1 | a0004c0008t0017g0184 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.830-1026_830-1025i others(80): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069366 | |||||
| chr11:69069366
|
GCCGTCTG others(32): Show |
G | 1 | a0001c0001t0010g0308 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.830-997_830-959del others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069366 | |||||
| chr11:69069368
|
C | T | 1 | a0004c0006t0009g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.830-1062C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069368 | ||||||
| chr11:69069369
|
G | A | 68 | a0003c0003t0002g0009a0003c0003t0002g0014a0003c0003t0002g0027others(65): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.830-1061G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069369 | ||||||
| chr11:69069381
|
G | A | 24 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(21): Show | 36 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.830-1049G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069381 | ||||||
| chr11:69069394
|
G | C | 1 | a0006c0007t0006g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.830-1036G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069394 | ||||||
| chr11:69069405
|
A | G | 44 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(41): Show | 54 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.830-1025A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069405 | ||||||
| chr11:69069412
|
G | C | 1 | a0004c0006t0009g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.830-1018G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069412 | ||||||
| chr11:69069421
|
G | C | 1 | a0004c0006t0009g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.830-1009G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069421 | ||||||
| chr11:69069426
|
G | T | 1 | a0003c0003t0002g0013 | 3 | HG01243.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.830-1004G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069426 | ||||||
| chr11:69069426
|
GACCGCAG others(71): Show |
G | 1 | a0002c0002t0029g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.830-926_830-849del others(78): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069426 | |||||
| chr11:69069427
|
ACCGCAGT others(72): Show |
A | 1 | a0004c0006t0009g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.830-1001_830-923de others(80): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069427 | |||||
| chr11:69069433
|
G | C | 7 | a0004c0008t0004g0105a0004c0008t0017g0183a0005c0004t0007g0141others(4): Show | 7 | HG01168.hp2 HG01255.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.830-997G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069433 | ||||||
| chr11:69069446
|
C | T | 1 | a0003c0003t0002g0013 | 3 | HG01243.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.830-984C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069446 | ||||||
| chr11:69069465
|
G | T | 3 | a0004c0008t0004g0105a0004c0008t0017g0183a0016c0036t0001g0187 | 3 | HG02258.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.830-965G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069465 | ||||||
| chr11:69069472
|
C | G | 38 | a0001c0001t0005g0289a0002c0002t0001g0043a0002c0002t0001g0243others(35): Show | 43 | HG01168.hp2 HG01192.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.830-958C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069472 | ||||||
| chr11:69069490
|
G | C | 3 | a0003c0003t0002g0013a0003c0003t0002g0137a0003c0003t0002g0160 | 5 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.830-940G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069490 | ||||||
| chr11:69069499
|
G | C | 4 | a0003c0003t0002g0013a0003c0003t0002g0137a0003c0003t0002g0160others(1): Show | 6 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.830-931G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069499 | ||||||
| chr11:69069499
|
G | GAAGTGAC others(265): Show |
1 | a0006c0007t0006g0169 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.830-927_830-926ins others(272): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069499 | |||||
| chr11:69069504
|
T | G | 121 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(118): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.830-926T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069504 | ||||||
| chr11:69069505
|
AC | A | 4 | a0003c0003t0002g0013a0003c0003t0002g0137a0003c0003t0002g0160others(1): Show | 6 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.830-923delC | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069505 | |||||
| chr11:69069508
|
G | A | 5 | a0003c0003t0002g0013a0003c0003t0002g0137a0003c0003t0002g0160others(2): Show | 7 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.830-922G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069508 | ||||||
| chr11:69069508
|
G | GCACTGGG others(265): Show |
1 | a0003c0003t0002g0135 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.830-920_830-919ins others(272): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069508 | |||||
| chr11:69069511
|
G | C | 21 | a0004c0008t0004g0105a0004c0008t0017g0183a0006c0007t0006g0004others(18): Show | 26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.830-919G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069511 | ||||||
| chr11:69069512
|
T | G | 6 | a0003c0003t0002g0013a0003c0003t0002g0135a0003c0003t0002g0137others(3): Show | 8 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.830-918T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069512 | ||||||
| chr11:69069512
|
T | TGGGAGCA others(31): Show |
5 | a0002c0002t0001g0043a0002c0002t0001g0243a0002c0002t0001g0244others(2): Show | 6 | HG01192.hp1 NA18956.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.830-893_830-892ins others(38): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069512 | |||||
| chr11:69069512
|
T | TGGGAGCA others(263): Show |
1 | a0002c0002t0001g0231 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.830-881_830-880ins others(270): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069512 | |||||
| chr11:69069512
|
T | TGGGAGCA others(265): Show |
1 | a0002c0002t0001g0264 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.830-881_830-880ins others(272): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069512 | |||||
| chr11:69069512
|
T | TGGGAGCA others(265): Show |
52 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0017others(49): Show | 68 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.830-881_830-880ins others(272): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069512 | |||||
| chr11:69069512
|
T | TGGGAGCA others(226): Show |
68 | a0003c0003t0002g0009a0003c0003t0002g0014a0003c0003t0002g0027others(65): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.830-881_830-880ins others(233): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069512 | |||||
| chr11:69069512
|
T | TGGGAGCA others(226): Show |
5 | a0002c0002t0001g0003a0002c0002t0023g0003a0002c0002t0026g0003others(2): Show | 9 | HG00621.hp2 HG02071.hp1 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.830-881_830-880ins others(233): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069512 | |||||
| chr11:69069512
|
T | TGGGAGCA others(265): Show |
1 | a0018c0022t0001g0240 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.830-881_830-880ins others(272): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069512 | |||||
| chr11:69069512
|
T | TGGGAGCA others(187): Show |
1 | a0009c0012t0002g0165 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.830-881_830-880ins others(194): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069512 | |||||
| chr11:69069543
|
G | A | 1 | a0004c0023t0019g0271 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.830-887G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069543 | ||||||
| chr11:69069546
|
C | CGCAGTGG others(226): Show |
1 | a0006c0007t0006g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.830-881_830-880ins others(233): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069546 | |||||
| chr11:69069546
|
C | T | 1 | a0006c0007t0006g0169 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.830-884C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069546 | ||||||
| chr11:69069550
|
C | A | 143 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(140): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.830-880C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069550 | ||||||
| chr11:69069550
|
C | CTGGGAGC others(304): Show |
6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.830-764_830-763ins others(311): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069550 | |||||
| chr11:69069550
|
C | CTGGGAGC others(32): Show |
2 | a0004c0008t0013g0196a0010c0014t0013g0200 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.830-842_830-841ins others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069550 | |||||
| chr11:69069550
|
C | CTGGGAGC others(304): Show |
6 | a0004c0008t0013g0194a0004c0008t0013g0197a0004c0008t0031g0195others(3): Show | 6 | HG01884.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.830-842_830-841ins others(311): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069550 | |||||
| chr11:69069550
|
C | CTGGGAGC others(304): Show |
1 | a0004c0006t0033g0207 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.830-842_830-841ins others(311): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069550 | |||||
| chr11:69069550
|
C | CTGGGAGC others(304): Show |
2 | a0004c0006t0019g0270a0004c0006t0020g0047 | 3 | HG02145.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.830-842_830-841ins others(311): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069550 | |||||
| chr11:69069550
|
C | CTGGGAGC others(304): Show |
11 | a0004c0011t0012g0201a0004c0011t0012g0203a0004c0011t0012g0204others(8): Show | 12 | HG02809.hp1 HG02886.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.830-842_830-841ins others(311): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069550 | |||||
| chr11:69069550
|
C | G | 54 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(51): Show | 66 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.830-880C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069550 | ||||||
| chr11:69069550
|
C | GTGGGAGC others(265): Show |
1 | a0002c0002t0001g0230 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.830-880delCinsGTGG others(269): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069550 | ||||||
| chr11:69069551
|
T | TGGAAGCA others(148): Show |
1 | a0005c0004t0007g0141 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.830-877_830-876ins others(155): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069551 | |||||
| chr11:69069551
|
T | TGGGAGCA others(187): Show |
13 | a0005c0004t0007g0026a0005c0004t0007g0037a0005c0004t0007g0111others(10): Show | 15 | HG00099.hp2 HG00741.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.830-842_830-841ins others(194): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069551 | |||||
| chr11:69069554
|
G | A | 1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.830-876G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069554 | ||||||
| chr11:69069563
|
C | T | 18 | a0001c0001t0004g0156a0001c0001t0004g0157a0001c0005t0004g0001others(15): Show | 27 | HG00423.hp1 HG01069.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.830-867C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069563 | ||||||
| chr11:69069589
|
C | A | 14 | a0005c0004t0007g0026a0005c0004t0007g0037a0005c0004t0007g0111others(11): Show | 16 | HG00099.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.830-841C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069589 | ||||||
| chr11:69069589
|
C | CTGGGAGC others(343): Show |
5 | a0004c0006t0009g0214a0004c0006t0009g0215a0004c0006t0009g0216others(2): Show | 5 | HG02622.hp1 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.830-725_830-724ins others(350): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069589 | |||||
| chr11:69069589
|
C | CTGGGAGC others(32): Show |
1 | a0002c0027t0001g0186 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.830-829_830-828ins others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069589 | |||||
| chr11:69069589
|
C | G | 121 | a0001c0001t0003g0007a0001c0001t0003g0060a0001c0001t0003g0068others(118): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.830-841C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069589 | ||||||
| chr11:69069590
|
T | TGGGAGCA others(109): Show |
1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.830-810_830-809ins others(116): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069590 | |||||
| chr11:69069628
|
G | A | 1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.830-802G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069628 | ||||||
| chr11:69069634
|
G | A | 1 | a0023c0041t0004g0088 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.830-796G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069634 | ||||||
| chr11:69069663
|
C | T | 40 | a0001c0001t0004g0290a0001c0001t0005g0011a0001c0001t0005g0048others(37): Show | 45 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.830-767C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069663 | ||||||
| chr11:69069664
|
G | A | 44 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(41): Show | 54 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.830-766G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069664 | ||||||
| chr11:69069664
|
G | GCAGTGGG others(226): Show |
3 | a0002c0027t0001g0186a0004c0008t0017g0184a0016c0036t0001g0187 | 3 | HG02486.hp2 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.830-725_830-724ins others(233): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069664 | |||||
| chr11:69069664
|
G | GCAGTGGG others(265): Show |
4 | a0004c0008t0004g0105a0004c0008t0013g0196a0004c0008t0017g0183others(1): Show | 4 | HG02258.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.830-725_830-724ins others(272): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069664 | |||||
| chr11:69069664
|
G | GCAGTGGG others(304): Show |
19 | a0006c0007t0006g0004a0006c0007t0006g0168a0006c0007t0006g0171others(16): Show | 24 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.830-725_830-724ins others(311): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069664 | |||||
| chr11:69069667
|
G | C | 24 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(21): Show | 36 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.830-763G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069667 | ||||||
| chr11:69069706
|
C | G | 85 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(82): Show | 106 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.830-724C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069706 | ||||||
| chr11:69069707
|
T | TGGGAGCA others(345): Show |
1 | a0004c0006t0009g0213 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.830-686_830-685ins others(352): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069707 | |||||
| chr11:69069742
|
G | T | 1 | a0001c0005t0042g0089 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.830-688G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069742 | ||||||
| chr11:69069745
|
C | G | 2 | a0003c0003t0002g0133a0004c0023t0019g0271 | 2 | HG01099.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.830-685C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069745 | ||||||
| chr11:69069780
|
C | G | 1 | a0002c0002t0001g0239 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.830-650C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069780 | ||||||
| chr11:69069784
|
C | G | 219 | a0001c0001t0003g0077a0001c0005t0004g0096a0002c0002t0001g0002others(216): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.830-646C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069784 | ||||||
| chr11:69069788
|
G | A | 108 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(105): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.830-642G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069788 | ||||||
| chr11:69069797
|
C | CGTCTCAG others(304): Show |
1 | a0004c0023t0019g0271 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.830-629_830-628ins others(311): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069797 | |||||
| chr11:69069797
|
C | CGTCTGAG others(32): Show |
1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.830-612_830-611ins others(39): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69069797 | |||||
| chr11:69069797
|
C | T | 217 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(214): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.830-633C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069797 | ||||||
| chr11:69069833
|
G | C | 3 | a0001c0001t0016g0018a0011c0017t0016g0018a0011c0017t0016g0285 | 4 | HG01934.hp1 HG02280.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.830-597G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069833 | ||||||
| chr11:69069861
|
G | C | 1 | a0001c0001t0010g0312 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.830-569G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069861 | ||||||
| chr11:69069861
|
G | GC | 323 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(320): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.830-569_830-568ins others(1): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069861 | ||||||
| chr11:69069900
|
G | A | 21 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(18): Show | 23 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.830-530G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069900 | ||||||
| chr11:69069951
|
G | C | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.830-479G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69069951 | ||||||
| chr11:69070026
|
CT | C | 109 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(106): Show | 135 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.830-392delT | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr11 | 69070026 | |||||
| chr11:69070046
|
A | G | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.830-384A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070046 | ||||||
| chr11:69070089
|
G | A | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.830-341G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070089 | ||||||
| chr11:69070093
|
C | T | 3 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0023t0019g0271 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.830-337C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070093 | ||||||
| chr11:69070094
|
G | A | 1 | a0002c0002t0001g0275 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.830-336G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070094 | ||||||
| chr11:69070184
|
C | T | 1 | a0003c0003t0002g0033 | 2 | NA19010.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.830-246C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070184 | ||||||
| chr11:69070280
|
C | G | 1 | a0001c0001t0005g0282 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.830-150C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070280 | ||||||
| chr11:69070326
|
A | G | 70 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(67): Show | 91 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.830-104A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070326 | ||||||
| chr11:69070407
|
C | A | 1 | a0004c0008t0017g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.830-23C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070407 | ||||||
| chr11:69070409
|
G | A | 1 | a0004c0008t0017g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.830-21G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070409 | ||||||
| chr11:69070413
|
T | C | 2 | a0003c0020t0002g0115a0003c0020t0002g0164 | 2 | NA19068.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.830-17T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 8/24 | chr11 | 69070413 | ||||||
| chr11:69070514
|
G | A | 1 | a0004c0006t0033g0207 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.895+19G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070514 | ||||||
| chr11:69070552
|
C | A | 1 | a0001c0001t0005g0286 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.895+57C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070552 | ||||||
| chr11:69070560
|
C | T | 109 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(106): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.895+65C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070560 | ||||||
| chr11:69070716
|
C | T | 1 | a0002c0002t0001g0245 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.895+221C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070716 | ||||||
| chr11:69070779
|
A | T | 1 | a0003c0003t0002g0132 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.895+284A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070779 | ||||||
| chr11:69070826
|
C | T | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.895+331C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070826 | ||||||
| chr11:69070852
|
C | T | 1 | a0002c0002t0001g0266 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.895+357C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070852 | ||||||
| chr11:69070954
|
A | C | 1 | a0002c0002t0001g0231 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.896-402A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070954 | ||||||
| chr11:69070962
|
G | A | 1 | a0001c0005t0004g0092 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.896-394G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070962 | ||||||
| chr11:69070995
|
C | G | 1 | a0004c0008t0001g0219 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.896-361C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69070995 | ||||||
| chr11:69071003
|
C | G | 109 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(106): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.896-353C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69071003 | ||||||
| chr11:69071089
|
GGCTTCAC others(21): Show |
G | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.896-214_896-187del others(28): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr11 | 69071089 | |||||
| chr11:69071130
|
G | A | 19 | a0006c0007t0006g0004a0006c0007t0006g0168a0006c0007t0006g0171others(16): Show | 24 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.896-226G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69071130 | ||||||
| chr11:69071269
|
C | T | 2 | a0002c0002t0001g0223a0002c0002t0001g0264 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.896-87C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69071269 | ||||||
| chr11:69071344
|
C | G | 6 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(3): Show | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.896-12C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 9/24 | chr11 | 69071344 | ||||||
| chr11:69071461
|
G | A | 1 | a0002c0002t0001g0257 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.960+41G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071461 | ||||||
| chr11:69071519
|
C | G | 2 | a0004c0006t0009g0192a0004c0006t0037g0191 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.960+99C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071519 | ||||||
| chr11:69071553
|
C | T | 1 | a0005c0004t0008g0109 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.960+133C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071553 | ||||||
| chr11:69071645
|
G | A | 4 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(1): Show | 6 | HG01346.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+225G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071645 | ||||||
| chr11:69071659
|
C | T | 12 | a0004c0008t0004g0105a0004c0008t0013g0194a0004c0008t0013g0196others(9): Show | 12 | HG01884.hp2 HG02258.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.960+239C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071659 | ||||||
| chr11:69071701
|
G | T | 3 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0023t0019g0271 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.961-222G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071701 | ||||||
| chr11:69071712
|
G | A | 3 | a0004c0006t0009g0016a0004c0006t0009g0192a0004c0006t0037g0191 | 5 | HG01891.hp2 HG02717.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.961-211G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071712 | ||||||
| chr11:69071719
|
T | C | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.961-204T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071719 | ||||||
| chr11:69071806
|
G | GC | 16 | a0001c0001t0011g0294a0001c0005t0004g0094a0002c0002t0001g0247others(13): Show | 16 | HG01934.hp2 HG02055.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.961-108dupC | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr11 | 69071806 | |||||
| chr11:69071808
|
C | G | 1 | a0001c0005t0042g0089 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.961-115C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071808 | ||||||
| chr11:69071814
|
C | G | 1 | a0002c0002t0001g0244 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.961-109C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071814 | ||||||
| chr11:69071843
|
G | A | 1 | a0005c0004t0038g0139 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.961-80G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071843 | ||||||
| chr11:69071866
|
G | A | 50 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(47): Show | 64 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.961-57G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 10/24 | chr11 | 69071866 | ||||||
| chr11:69072024
|
G | GTGAGTGC others(6): Show |
1 | a0002c0002t0001g0231 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1061+4_1061+16dupA others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr11 | 69072024 | |||||
| chr11:69072077
|
G | A | 1 | a0005c0004t0008g0138 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1061+54G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072077 | ||||||
| chr11:69072087
|
C | T | 35 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(32): Show | 45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1061+64C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072087 | ||||||
| chr11:69072175
|
C | A | 7 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(4): Show | 7 | HG02572.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1061+152C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072175 | ||||||
| chr11:69072191
|
G | A | 3 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0023t0019g0271 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1061+168G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072191 | ||||||
| chr11:69072192
|
C | T | 2 | a0003c0042t0002g0099a0006c0030t0006g0167 | 2 | HG03834.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1061+169C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072192 | ||||||
| chr11:69072226
|
G | GC | 89 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(86): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1061+209dupC | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr11 | 69072226 | |||||
| chr11:69072233
|
G | C | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1061+210G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072233 | ||||||
| chr11:69072254
|
G | A | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1061+231G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072254 | ||||||
| chr11:69072257
|
C | T | 1 | a0001c0001t0005g0272 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1061+234C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072257 | ||||||
| chr11:69072378
|
C | T | 1 | a0002c0002t0001g0259 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1062-249C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072378 | ||||||
| chr11:69072442
|
G | C | 21 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(18): Show | 30 | HG00423.hp1 HG00438.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1062-185G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072442 | ||||||
| chr11:69072455
|
C | T | 35 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(32): Show | 45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1062-172C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072455 | ||||||
| chr11:69072481
|
C | T | 109 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(106): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1062-146C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072481 | ||||||
| chr11:69072546
|
G | A | 101 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(98): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1062-81G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072546 | ||||||
| chr11:69072581
|
G | T | 1 | a0002c0002t0001g0256 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1062-46G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072581 | ||||||
| chr11:69072582
|
A | C | 1 | a0002c0002t0001g0256 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1062-45A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072582 | ||||||
| chr11:69072600
|
C | T | 3 | a0010c0014t0013g0198a0010c0014t0013g0199a0010c0014t0013g0200 | 3 | HG01884.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1062-27C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072600 | ||||||
| chr11:69072603
|
C | T | 35 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(32): Show | 45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1062-24C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 11/24 | chr11 | 69072603 | ||||||
| chr11:69072775
|
T | C | 1 | a0003c0003t0002g0117 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1143+67T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 12/24 | chr11 | 69072775 | ||||||
| chr11:69072846
|
GGGGCGCT others(9): Show |
G | 2 | a0004c0008t0013g0196a0004c0008t0013g0197 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1144-54_1144-39del others(16): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr11 | 69072846 | |||||
| chr11:69072854
|
C | T | 1 | a0001c0001t0004g0157 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1144-61C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 12/24 | chr11 | 69072854 | ||||||
| chr11:69073022
|
C | T | 2 | a0003c0003t0002g0137a0003c0003t0002g0160 | 2 | HG02109.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1230+21C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073022 | ||||||
| chr11:69073041
|
C | G | 1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+40C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073041 | ||||||
| chr11:69073046
|
C | A | 1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+45C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073046 | ||||||
| chr11:69073051
|
T | G | 1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+50T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073051 | ||||||
| chr11:69073052
|
C | A | 1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+51C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073052 | ||||||
| chr11:69073053
|
C | T | 1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+52C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073053 | ||||||
| chr11:69073058
|
C | A | 1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+57C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073058 | ||||||
| chr11:69073076
|
A | T | 1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+75A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073076 | ||||||
| chr11:69073081
|
T | G | 1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+80T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073081 | ||||||
| chr11:69073085
|
A | C | 1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+84A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073085 | ||||||
| chr11:69073095
|
C | A | 1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+94C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073095 | ||||||
| chr11:69073103
|
C | A | 1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+102C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073103 | ||||||
| chr11:69073104
|
ACCTGCCA others(21): Show |
A | 1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+104_1230+131d others(30): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073104 | ||||||
| chr11:69073149
|
T | A | 112 | a0001c0001t0005g0286a0001c0001t0005g0287a0003c0003t0002g0009others(109): Show | 138 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1230+148T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073149 | ||||||
| chr11:69073179
|
T | G | 1 | a0001c0001t0003g0076 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1230+178T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073179 | ||||||
| chr11:69073236
|
G | T | 1 | a0004c0006t0007g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1230+235G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073236 | ||||||
| chr11:69073399
|
A | G | 12 | a0004c0008t0004g0105a0004c0008t0013g0194a0004c0008t0013g0196others(9): Show | 12 | HG01884.hp2 HG02258.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1230+398A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073399 | ||||||
| chr11:69073448
|
T | C | 122 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(119): Show | 149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1230+447T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073448 | ||||||
| chr11:69073671
|
G | A | 1 | a0003c0003t0002g0143 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1230+670G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073671 | ||||||
| chr11:69073774
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1230+773C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073774 | ||||||
| chr11:69073780
|
CTGTAGAT others(45): Show |
C | 1 | a0003c0003t0002g0107 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1230+826_1230+877d others(54): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69073780 | |||||
| chr11:69073789
|
C | A | 11 | a0001c0001t0003g0006a0001c0001t0003g0019a0001c0001t0003g0058others(8): Show | 14 | HG00733.hp2 HG01070.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1230+788C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073789 | ||||||
| chr11:69073834
|
G | A | 1 | a0001c0001t0003g0062 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1230+833G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073834 | ||||||
| chr11:69073844
|
G | C | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1230+843G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69073844 | ||||||
| chr11:69073974
|
AG | A | 85 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(82): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1230+976delG | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69073974 | |||||
| chr11:69074103
|
A | G | 219 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(216): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1230+1102A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074103 | ||||||
| chr11:69074205
|
C | T | 1 | a0004c0006t0007g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1230+1204C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074205 | ||||||
| chr11:69074219
|
T | G | 323 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(320): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.1230+1218T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074219 | ||||||
| chr11:69074262
|
G | C | 1 | a0001c0001t0005g0295 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1230+1261G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074262 | ||||||
| chr11:69074340
|
G | A | 1 | a0004c0013t0015g0208 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1230+1339G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074340 | ||||||
| chr11:69074341
|
C | T | 1 | a0002c0002t0001g0244 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1230+1340C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074341 | ||||||
| chr11:69074421
|
T | C | 2 | a0003c0003t0002g0124a0003c0003t0002g0132 | 2 | NA18959.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1230+1420T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074421 | ||||||
| chr11:69074428
|
T | C | 1 | a0001c0001t0003g0022 | 2 | NA18974.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.1230+1427T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074428 | ||||||
| chr11:69074451
|
T | TA | 36 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(33): Show | 46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1230+1451dupA | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69074451 | |||||
| chr11:69074490
|
T | C | 8 | a0003c0003t0002g0031a0003c0003t0002g0113a0003c0003t0002g0120others(5): Show | 9 | HG00558.hp1 NA18947.hp1 NA18973.hp2 others(6): Show |
intron_variant | MODIFIER | c.1230+1489T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074490 | ||||||
| chr11:69074525
|
A | G | 109 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(106): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1230+1524A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074525 | ||||||
| chr11:69074553
|
C | T | 6 | a0003c0003t0002g0014a0003c0003t0002g0027a0003c0003t0002g0129others(3): Show | 9 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(6): Show |
intron_variant | MODIFIER | c.1230+1552C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074553 | ||||||
| chr11:69074560
|
C | T | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1230+1559C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074560 | ||||||
| chr11:69074580
|
GA | G | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1230+1581delA | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69074580 | |||||
| chr11:69074630
|
A | C | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1230+1629A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074630 | ||||||
| chr11:69074654
|
G | C | 1 | a0004c0006t0007g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1230+1653G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074654 | ||||||
| chr11:69074715
|
T | G | 4 | a0004c0013t0015g0038a0004c0013t0015g0208a0004c0013t0015g0209others(1): Show | 5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1230+1714T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074715 | ||||||
| chr11:69074982
|
C | T | 24 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(21): Show | 36 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1230+1981C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69074982 | ||||||
| chr11:69075004
|
C | T | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1230+2003C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075004 | ||||||
| chr11:69075023
|
G | A | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1230+2022G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075023 | ||||||
| chr11:69075127
|
T | C | 36 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(33): Show | 46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1230+2126T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075127 | ||||||
| chr11:69075153
|
G | A | 7 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(4): Show | 7 | HG02572.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1230+2152G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075153 | ||||||
| chr11:69075229
|
T | C | 1 | a0001c0001t0003g0068 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1230+2228T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075229 | ||||||
| chr11:69075236
|
A | G | 22 | a0004c0008t0017g0184a0006c0007t0006g0004a0006c0007t0006g0168others(19): Show | 27 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1230+2235A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075236 | ||||||
| chr11:69075418
|
A | G | 36 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(33): Show | 46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1230+2417A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075418 | ||||||
| chr11:69075433
|
A | G | 280 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(277): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1230+2432A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075433 | ||||||
| chr11:69075451
|
A | G | 1 | a0002c0002t0001g0238 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1230+2450A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075451 | ||||||
| chr11:69075535
|
G | A | 27 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(24): Show | 32 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1230+2534G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075535 | ||||||
| chr11:69075544
|
G | C | 36 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(33): Show | 46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1230+2543G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075544 | ||||||
| chr11:69075651
|
G | A | 116 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(113): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1230+2650G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075651 | ||||||
| chr11:69075720
|
C | T | 7 | a0004c0011t0012g0201a0004c0011t0012g0203a0004c0011t0012g0204others(4): Show | 7 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1230+2719C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075720 | ||||||
| chr11:69075743
|
C | T | 1 | a0018c0022t0001g0240 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1231-2739C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075743 | ||||||
| chr11:69075744
|
G | A | 1 | a0004c0006t0019g0270 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1231-2738G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075744 | ||||||
| chr11:69075760
|
C | T | 2 | a0002c0002t0001g0040a0002c0033t0001g0040 | 2 | HG00735.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1231-2722C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075760 | ||||||
| chr11:69075802
|
T | G | 1 | a0002c0002t0001g0252 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1231-2680T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075802 | ||||||
| chr11:69075892
|
C | T | 1 | a0003c0003t0002g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1231-2590C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075892 | ||||||
| chr11:69075946
|
G | A | 9 | a0005c0004t0007g0037a0005c0004t0007g0141a0005c0004t0007g0142others(6): Show | 10 | HG00099.hp2 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1231-2536G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075946 | ||||||
| chr11:69075955
|
T | C | 4 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(1): Show | 6 | HG01346.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-2527T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69075955 | ||||||
| chr11:69076138
|
A | G | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-2344A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076138 | ||||||
| chr11:69076239
|
C | T | 2 | a0003c0003t0002g0181a0003c0003t0002g0182 | 2 | NA18974.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.1231-2243C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076239 | ||||||
| chr11:69076240
|
G | A | 7 | a0004c0011t0012g0201a0004c0011t0012g0203a0004c0011t0012g0204others(4): Show | 7 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-2242G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076240 | ||||||
| chr11:69076243
|
C | T | 89 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(86): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1231-2239C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076243 | ||||||
| chr11:69076247
|
G | A | 3 | a0005c0004t0007g0026a0005c0004t0007g0268a0005c0004t0007g0269 | 4 | HG00741.hp1 HG01123.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-2235G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076247 | ||||||
| chr11:69076272
|
C | G | 6 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(3): Show | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-2210C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076272 | ||||||
| chr11:69076280
|
G | A | 1 | a0001c0001t0004g0290 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1231-2202G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076280 | ||||||
| chr11:69076324
|
C | T | 1 | a0003c0003t0002g0166 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1231-2158C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076324 | ||||||
| chr11:69076378
|
T | G | 1 | a0001c0005t0004g0091 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1231-2104T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076378 | ||||||
| chr11:69076445
|
C | G | 219 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(216): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1231-2037C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076445 | ||||||
| chr11:69076464
|
C | T | 68 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(65): Show | 89 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1231-2018C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076464 | ||||||
| chr11:69076522
|
G | A | 84 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(81): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1231-1960G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076522 | ||||||
| chr11:69076528
|
C | G | 1 | a0002c0029t0001g0273 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1231-1954C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076528 | ||||||
| chr11:69076538
|
GCCTGCCC others(18): Show |
G | 1 | a0005c0004t0007g0154 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1231-1905_1231-188 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076538 | |||||
| chr11:69076553
|
C | CTGTCCCT others(358): Show |
3 | a0006c0007t0006g0175a0006c0007t0006g0176a0006c0007t0006g0177 | 3 | HG02698.hp2 HG02738.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1231-1906_1231-190 others(369): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076553 | |||||
| chr11:69076553
|
C | CTGTCCCT others(383): Show |
17 | a0006c0007t0006g0004a0006c0007t0006g0168a0006c0007t0006g0169others(14): Show | 22 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1231-1906_1231-190 others(394): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076553 | |||||
| chr11:69076555
|
G | A | 12 | a0004c0008t0004g0105a0004c0008t0013g0194a0004c0008t0013g0196others(9): Show | 12 | HG01884.hp2 HG02258.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1231-1927G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076555 | ||||||
| chr11:69076575
|
G | C | 66 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(63): Show | 86 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1231-1907G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076575 | ||||||
| chr11:69076577
|
T | C | 134 | a0002c0002t0001g0042a0002c0002t0001g0221a0002c0027t0001g0186others(131): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1231-1905T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076577 | ||||||
| chr11:69076578
|
C | A | 22 | a0002c0027t0001g0186a0006c0007t0006g0004a0006c0007t0006g0168others(19): Show | 27 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1231-1904C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076578 | ||||||
| chr11:69076578
|
C | G | 112 | a0002c0002t0001g0042a0002c0002t0001g0221a0003c0003t0002g0009others(109): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1231-1904C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076578 | ||||||
| chr11:69076579
|
T | C | 2 | a0002c0027t0001g0186a0016c0036t0001g0187 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1231-1903T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076579 | ||||||
| chr11:69076588
|
A | ACCTGCCC others(308): Show |
1 | a0013c0043t0025g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1231-1881_1231-188 others(319): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076588 | |||||
| chr11:69076602
|
C | G | 111 | a0002c0002t0001g0042a0002c0002t0001g0221a0003c0003t0002g0009others(108): Show | 138 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1231-1880C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076602 | ||||||
| chr11:69076627
|
G | A | 35 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(32): Show | 45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1231-1855G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076627 | ||||||
| chr11:69076627
|
G | C | 131 | a0002c0002t0001g0042a0002c0002t0001g0221a0003c0003t0002g0009others(128): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1231-1855G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076627 | ||||||
| chr11:69076627
|
GGTGTCCC others(18): Show |
G | 44 | a0001c0001t0004g0290a0001c0001t0005g0011a0001c0001t0005g0048others(41): Show | 49 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1231-1780_1231-175 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076627 | |||||
| chr11:69076638
|
A | ACCTGCCC others(100): Show |
2 | a0004c0006t0019g0270a0004c0006t0020g0047 | 3 | HG02145.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1231-1830_1231-182 others(111): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076638 | |||||
| chr11:69076648
|
C | CTGCCCTC others(67): Show |
1 | a0004c0023t0019g0271 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1231-1830_1231-182 others(78): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076648 | |||||
| chr11:69076653
|
G | A | 3 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0023t0019g0271 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-1829G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076653 | ||||||
| chr11:69076663
|
A | ACTTGCCC others(1): Show |
3 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0023t0019g0271 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-1818_1231-181 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076663 | |||||
| chr11:69076677
|
C | T | 2 | a0004c0008t0004g0105a0004c0008t0017g0183 | 2 | HG02258.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1231-1805C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076677 | ||||||
| chr11:69076678
|
G | A | 3 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0023t0019g0271 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-1804G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076678 | ||||||
| chr11:69076690
|
C | T | 3 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0023t0019g0271 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-1792C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076690 | ||||||
| chr11:69076701
|
C | G | 1 | a0004c0006t0009g0216 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1231-1781C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076701 | ||||||
| chr11:69076702
|
C | T | 35 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(32): Show | 45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1231-1780C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076702 | ||||||
| chr11:69076702
|
CGTGTCCC others(18): Show |
C | 7 | a0004c0008t0013g0197a0004c0015t0014g0051a0004c0015t0014g0052others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1231-1730_1231-170 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076702 | |||||
| chr11:69076703
|
G | A | 3 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0023t0019g0271 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-1779G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076703 | ||||||
| chr11:69076706
|
T | C | 3 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0023t0019g0271 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-1776T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076706 | ||||||
| chr11:69076706
|
T | TCCCTCCA others(150): Show |
82 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(79): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1231-1756_1231-175 others(161): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076706 | |||||
| chr11:69076706
|
T | TCCCTCCA others(142): Show |
1 | a0005c0004t0007g0161 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1231-1756_1231-175 others(153): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076706 | |||||
| chr11:69076706
|
T | TCCCTCCA others(175): Show |
6 | a0004c0011t0012g0203a0004c0011t0012g0204a0004c0011t0012g0205others(3): Show | 6 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-1756_1231-175 others(186): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076706 | |||||
| chr11:69076721
|
TCCTGCTG others(60): Show |
T | 10 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(7): Show | 12 | HG01346.hp2 HG01891.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1231-1755_1231-168 others(71): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076721 | |||||
| chr11:69076725
|
G | GCCCTCCT others(122): Show |
5 | a0004c0013t0015g0038a0004c0013t0015g0208a0004c0013t0015g0209others(2): Show | 6 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-1756_1231-175 others(133): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076725 | |||||
| chr11:69076727
|
T | C | 130 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(127): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1231-1755T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076727 | ||||||
| chr11:69076728
|
G | A | 26 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(23): Show | 38 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1231-1754G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076728 | ||||||
| chr11:69076728
|
G | GCCA | 6 | a0004c0013t0015g0038a0004c0013t0015g0208a0004c0013t0015g0209others(3): Show | 7 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-1754_1231-175 others(7): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076728 | ||||||
| chr11:69076729
|
T | C | 26 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(23): Show | 38 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1231-1753T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076729 | ||||||
| chr11:69076731
|
T | C | 5 | a0004c0013t0015g0038a0004c0013t0015g0208a0004c0013t0015g0209others(2): Show | 6 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-1751T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076731 | ||||||
| chr11:69076746
|
TCCTGCTG others(10): Show |
T | 1 | a0004c0011t0012g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1231-1730_1231-171 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076746 | |||||
| chr11:69076750
|
G | GCCCTC | 26 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(23): Show | 38 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1231-1731_1231-173 others(9): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076750 | |||||
| chr11:69076752
|
T | C | 236 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(233): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1231-1730T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076752 | ||||||
| chr11:69076753
|
G | A | 1 | a0005c0004t0007g0149 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1729G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076753 | ||||||
| chr11:69076753
|
G | GCCA | 27 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(24): Show | 39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1729_1231-172 others(7): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076753 | ||||||
| chr11:69076754
|
T | C | 1 | a0005c0004t0007g0149 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1728T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076754 | ||||||
| chr11:69076771
|
TCCTGCCG others(10): Show |
T | 6 | a0001c0001t0003g0066a0001c0001t0003g0067a0002c0002t0001g0042others(3): Show | 7 | HG00741.hp2 HG01167.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-1704_1231-168 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076771 | |||||
| chr11:69076773
|
C | G | 26 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(23): Show | 38 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1231-1709C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076773 | ||||||
| chr11:69076778
|
G | A | 163 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(160): Show | 208 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1231-1704G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076778 | ||||||
| chr11:69076779
|
T | C | 91 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(88): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1231-1703T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076779 | ||||||
| chr11:69076788
|
A | ACCTGCCC others(1): Show |
91 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(88): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1231-1687_1231-168 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076788 | |||||
| chr11:69076788
|
A | ACTTGCCC others(1): Show |
27 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(24): Show | 39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1693_1231-169 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076788 | |||||
| chr11:69076789
|
C | CCTGCCCT others(607): Show |
1 | a0006c0007t0006g0188 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1231-1532_1231-153 others(618): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076789 | |||||
| chr11:69076789
|
C | CCTGCCCT others(922): Show |
3 | a0008c0010t0006g0100a0008c0010t0006g0101a0008c0010t0006g0102 | 3 | HG00099.hp1 HG00323.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1231-1456_1231-145 others(933): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076789 | |||||
| chr11:69076789
|
C | CCTGCCCT others(607): Show |
1 | a0006c0007t0006g0168 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1231-1456_1231-145 others(618): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076789 | |||||
| chr11:69076789
|
C | CCTGCCCT others(607): Show |
15 | a0006c0007t0006g0004a0006c0007t0006g0169a0006c0007t0006g0171others(12): Show | 20 | HG00735.hp2 HG01167.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.1231-1456_1231-145 others(618): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076789 | |||||
| chr11:69076789
|
C | CCTGCCCT others(682): Show |
1 | a0013c0043t0025g0104 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1231-1680_1231-167 others(693): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076789 | |||||
| chr11:69076798
|
C | CTGCCCTC others(1): Show |
109 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(106): Show | 139 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1231-1680_1231-167 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076798 | |||||
| chr11:69076798
|
C | CTGCCCTC others(34): Show |
1 | a0002c0002t0001g0189 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1231-1680_1231-167 others(45): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076798 | |||||
| chr11:69076798
|
C | G | 6 | a0001c0001t0003g0066a0001c0001t0003g0067a0002c0002t0001g0042others(3): Show | 7 | HG00741.hp2 HG01167.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-1684C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076798 | ||||||
| chr11:69076804
|
T | C | 6 | a0004c0013t0015g0038a0004c0013t0015g0208a0004c0013t0015g0209others(3): Show | 7 | HG02523.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-1678T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076804 | ||||||
| chr11:69076815
|
C | T | 143 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(140): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1231-1667C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076815 | ||||||
| chr11:69076831
|
G | A | 58 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(55): Show | 70 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1231-1651G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076831 | ||||||
| chr11:69076831
|
G | C | 32 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(29): Show | 45 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1231-1651G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076831 | ||||||
| chr11:69076848
|
T | C | 32 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(29): Show | 45 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1231-1634T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076848 | ||||||
| chr11:69076854
|
T | TCCTGCCA others(10): Show |
26 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(23): Show | 38 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1231-1622_1231-162 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076854 | |||||
| chr11:69076856
|
C | CTGCCCTC others(18): Show |
4 | a0004c0013t0015g0038a0004c0013t0015g0208a0004c0013t0015g0209others(1): Show | 5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-1619_1231-161 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076856 | |||||
| chr11:69076864
|
A | C | 157 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(154): Show | 203 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1231-1618A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076864 | ||||||
| chr11:69076864
|
A | G | 5 | a0002c0002t0001g0189a0002c0002t0001g0229a0002c0002t0001g0258others(2): Show | 5 | HG00642.hp1 HG01099.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-1618A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076864 | ||||||
| chr11:69076869
|
A | G | 27 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(24): Show | 39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1613A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076869 | ||||||
| chr11:69076897
|
C | A | 36 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(33): Show | 46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1231-1585C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076897 | ||||||
| chr11:69076900
|
C | T | 27 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(24): Show | 39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1582C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076900 | ||||||
| chr11:69076901
|
C | T | 27 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(24): Show | 39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1581C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076901 | ||||||
| chr11:69076902
|
A | G | 27 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(24): Show | 39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1580A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076902 | ||||||
| chr11:69076907
|
C | T | 27 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(24): Show | 39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1575C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076907 | ||||||
| chr11:69076908
|
C | G | 27 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(24): Show | 39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1574C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076908 | ||||||
| chr11:69076914
|
T | C | 95 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(92): Show | 119 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1231-1568T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076914 | ||||||
| chr11:69076914
|
T | TTGCCCTC others(1): Show |
37 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(34): Show | 47 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.1231-1563_1231-155 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076914 | |||||
| chr11:69076914
|
T | TTTCCCTC others(1): Show |
27 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(24): Show | 39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1567_1231-156 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076914 | |||||
| chr11:69076930
|
C | T | 124 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(121): Show | 160 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1231-1552C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076930 | ||||||
| chr11:69076942
|
C | T | 1 | a0001c0001t0003g0067 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1231-1540C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076942 | ||||||
| chr11:69076951
|
T | C | 124 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(121): Show | 160 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1231-1531T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076951 | ||||||
| chr11:69076952
|
G | A | 1 | a0005c0004t0007g0149 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1530G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076952 | ||||||
| chr11:69076952
|
G | GTGTCCCT others(134): Show |
15 | a0003c0003t0002g0034a0003c0003t0002g0126a0003c0003t0002g0129others(12): Show | 18 | HG01243.hp2 HG01346.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1231-1519_1231-151 others(145): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076952 | |||||
| chr11:69076962
|
A | ACTTGCCC others(34): Show |
81 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(78): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1231-1519_1231-151 others(45): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69076962 | |||||
| chr11:69076975
|
C | T | 27 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(24): Show | 39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1507C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076975 | ||||||
| chr11:69076976
|
C | T | 27 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(24): Show | 39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1506C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076976 | ||||||
| chr11:69076977
|
A | G | 40 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(37): Show | 54 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.1231-1505A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076977 | ||||||
| chr11:69076982
|
C | T | 27 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(24): Show | 39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1500C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076982 | ||||||
| chr11:69076983
|
C | G | 27 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(24): Show | 39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1499C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076983 | ||||||
| chr11:69076989
|
C | T | 28 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(25): Show | 40 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1231-1493C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69076989 | ||||||
| chr11:69077002
|
A | G | 82 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(79): Show | 103 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1231-1480A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077002 | ||||||
| chr11:69077003
|
C | T | 109 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(106): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1231-1479C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077003 | ||||||
| chr11:69077007
|
C | T | 1 | a0005c0004t0007g0149 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1475C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077007 | ||||||
| chr11:69077008
|
C | G | 1 | a0005c0004t0007g0149 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1474C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077008 | ||||||
| chr11:69077012
|
ACCTGCCC others(1): Show |
A | 27 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(24): Show | 39 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1455_1231-144 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077012 | |||||
| chr11:69077014
|
C | T | 1 | a0005c0004t0007g0149 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1468C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077014 | ||||||
| chr11:69077016
|
G | T | 1 | a0005c0004t0007g0149 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1466G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077016 | ||||||
| chr11:69077020
|
T | TCCTGTTG others(35): Show |
28 | a0004c0006t0007g0150a0004c0006t0019g0270a0004c0006t0033g0207others(25): Show | 33 | HG00099.hp2 HG00621.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1231-1458_1231-145 others(46): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077020 | |||||
| chr11:69077022
|
C | CTGTTGTG others(10): Show |
53 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(50): Show | 69 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1231-1458_1231-145 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077022 | |||||
| chr11:69077045
|
A | ACCTGCCC others(1): Show |
12 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(9): Show | 14 | HG01106.hp1 HG01346.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1231-1435_1231-142 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077045 | |||||
| chr11:69077055
|
G | C | 110 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(107): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1231-1427G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077055 | ||||||
| chr11:69077055
|
G | T | 14 | a0003c0003t0002g0034a0003c0003t0002g0126a0003c0003t0002g0129others(11): Show | 17 | HG01346.hp1 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1231-1427G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077055 | ||||||
| chr11:69077060
|
A | G | 1 | a0005c0004t0007g0149 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1422A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077060 | ||||||
| chr11:69077061
|
T | C | 70 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(67): Show | 90 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1231-1421T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077061 | ||||||
| chr11:69077070
|
ACTTGCCC others(1): Show |
A | 52 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(49): Show | 67 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1231-1410_1231-140 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077070 | |||||
| chr11:69077072
|
T | C | 72 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(69): Show | 93 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1231-1410T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077072 | ||||||
| chr11:69077078
|
T | TCCTGCCA others(43): Show |
1 | a0003c0003t0002g0031 | 2 | NA18973.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1231-1398_1231-139 others(54): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077078 | |||||
| chr11:69077078
|
T | TCCTGCCA others(110): Show |
3 | a0004c0013t0015g0038a0004c0013t0015g0208a0004c0013t0015g0211 | 4 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1398_1231-139 others(121): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077078 | |||||
| chr11:69077078
|
T | TCCTGTTG others(60): Show |
1 | a0005c0004t0007g0149 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1400_1231-139 others(71): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077078 | |||||
| chr11:69077094
|
T | C | 58 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(55): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1231-1388T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077094 | ||||||
| chr11:69077094
|
T | TGTCCCTC others(68): Show |
1 | a0003c0003t0002g0129 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1231-1378_1231-137 others(79): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077094 | |||||
| chr11:69077094
|
T | TGTCCCTC others(284): Show |
1 | a0001c0001t0003g0063 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1231-1378_1231-137 others(295): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077094 | |||||
| chr11:69077094
|
T | TGTCCCTC others(18): Show |
51 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(48): Show | 68 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1231-1378_1231-137 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077094 | |||||
| chr11:69077103
|
ACTTGCCC others(1): Show |
A | 3 | a0001c0005t0004g0097a0004c0006t0036g0218a0023c0041t0004g0088 | 3 | HG01243.hp2 HG02717.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1231-1377_1231-137 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077103 | |||||
| chr11:69077105
|
T | C | 122 | a0001c0001t0003g0063a0001c0001t0004g0155a0001c0001t0004g0156others(119): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.1231-1377T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077105 | ||||||
| chr11:69077105
|
T | TTGCCCTC others(301): Show |
1 | a0001c0001t0005g0287 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(312): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | |||||
| chr11:69077105
|
T | TTGCCCTC others(432): Show |
1 | a0002c0002t0001g0244 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(443): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | |||||
| chr11:69077105
|
T | TTGCCCTC others(317): Show |
27 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(24): Show | 37 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(328): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | |||||
| chr11:69077105
|
T | TTGCCCTC others(317): Show |
2 | a0001c0001t0003g0065a0001c0001t0003g0071 | 2 | HG02074.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(328): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | |||||
| chr11:69077105
|
T | TTGCCCTC others(342): Show |
6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(353): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | |||||
| chr11:69077105
|
T | TTGCCCTC others(408): Show |
19 | a0006c0007t0006g0168a0006c0007t0006g0169a0006c0007t0006g0171others(16): Show | 20 | HG00099.hp1 HG00323.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(419): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | |||||
| chr11:69077105
|
T | TTGCCCTC others(1007): Show |
1 | a0006c0007t0006g0004 | 5 | HG01167.hp1 HG01169.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(1018): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | |||||
| chr11:69077105
|
T | TTGCCCTC others(350): Show |
1 | a0006c0007t0006g0173 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(361): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | |||||
| chr11:69077105
|
T | TTGCCCTC others(325): Show |
38 | a0001c0001t0004g0290a0001c0001t0005g0272a0001c0001t0005g0277others(35): Show | 39 | HG00544.hp2 HG01106.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(336): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | |||||
| chr11:69077105
|
T | TTGCCCTC others(300): Show |
7 | a0001c0001t0005g0011a0001c0001t0005g0286a0001c0001t0005g0288others(4): Show | 10 | NA18612.hp1 NA18942.hp1 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(311): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | |||||
| chr11:69077105
|
T | TTGCCCTC others(325): Show |
10 | a0001c0001t0005g0048a0001c0001t0010g0284a0001c0001t0010g0307others(7): Show | 11 | HG00558.hp2 HG00597.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(336): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | |||||
| chr11:69077105
|
T | TTGCCCTC others(341): Show |
5 | a0002c0002t0001g0017a0002c0002t0001g0263a0002c0002t0001g0275others(2): Show | 7 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(352): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | |||||
| chr11:69077105
|
T | TTGCCCTC others(457): Show |
57 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(54): Show | 76 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(468): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | |||||
| chr11:69077105
|
T | TTGCCCTC others(456): Show |
1 | a0002c0002t0001g0249 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(467): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | |||||
| chr11:69077105
|
T | TTGCCCTC others(458): Show |
1 | a0002c0002t0001g0230 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(469): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | |||||
| chr11:69077105
|
T | TTGCCCTC others(482): Show |
1 | a0002c0002t0001g0266 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(493): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | |||||
| chr11:69077105
|
T | TTGCCCTC others(325): Show |
3 | a0010c0014t0013g0198a0010c0014t0013g0199a0010c0014t0013g0200 | 3 | HG01884.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1231-1332_1231-133 others(336): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077105 | |||||
| chr11:69077111
|
T | TCCTGCCA others(10): Show |
3 | a0003c0003t0002g0034a0003c0003t0002g0126a0003c0003t0002g0166 | 4 | HG01346.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1365_1231-136 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077111 | |||||
| chr11:69077111
|
T | TCCTGCCC others(325): Show |
1 | a0001c0001t0005g0274 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(336): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077111 | |||||
| chr11:69077111
|
T | TCCTGCCG others(10): Show |
6 | a0004c0011t0012g0203a0004c0011t0012g0204a0004c0011t0012g0205others(3): Show | 6 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-1365_1231-136 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077111 | |||||
| chr11:69077111
|
T | TCCTGCCG others(143): Show |
1 | a0004c0006t0020g0047 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1231-1365_1231-136 others(154): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077111 | |||||
| chr11:69077111
|
T | TCTTGCCA others(10): Show |
1 | a0004c0013t0015g0209 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1231-1370_1231-136 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077111 | |||||
| chr11:69077121
|
C | T | 3 | a0001c0005t0004g0097a0004c0006t0036g0218a0023c0041t0004g0088 | 3 | HG01243.hp2 HG02717.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1231-1361C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077121 | ||||||
| chr11:69077126
|
A | G | 7 | a0004c0006t0020g0047a0004c0011t0012g0203a0004c0011t0012g0204others(4): Show | 8 | HG02809.hp1 HG02895.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1231-1356A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077126 | ||||||
| chr11:69077127
|
T | C | 3 | a0001c0005t0004g0097a0004c0006t0036g0218a0023c0041t0004g0088 | 3 | HG01243.hp2 HG02717.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1231-1355T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077127 | ||||||
| chr11:69077129
|
T | TCCCTCCA others(459): Show |
1 | a0002c0002t0001g0243 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(470): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077129 | |||||
| chr11:69077134
|
C | T | 6 | a0004c0011t0012g0203a0004c0011t0012g0204a0004c0011t0012g0205others(3): Show | 6 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231-1348C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077134 | ||||||
| chr11:69077136
|
A | ACCTGCCC others(1): Show |
3 | a0001c0005t0004g0097a0004c0006t0036g0218a0023c0041t0004g0088 | 3 | HG01243.hp2 HG02717.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1231-1339_1231-133 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077136 | |||||
| chr11:69077136
|
A | ACCTGCCC others(26): Show |
1 | a0005c0004t0007g0149 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1231-1337_1231-133 others(37): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077136 | |||||
| chr11:69077144
|
T | TCCTGCCA others(319): Show |
1 | a0001c0001t0003g0075 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1231-1332_1231-133 others(330): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077144 | |||||
| chr11:69077146
|
C | T | 53 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(50): Show | 69 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1231-1336C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077146 | ||||||
| chr11:69077151
|
G | A | 80 | a0001c0001t0003g0019a0001c0001t0003g0072a0001c0001t0003g0078others(77): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1231-1331G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077151 | ||||||
| chr11:69077152
|
T | C | 56 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(53): Show | 73 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1231-1330T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077152 | ||||||
| chr11:69077161
|
A | ACCTGCCC others(1): Show |
56 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(53): Show | 73 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1231-1314_1231-130 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077161 | |||||
| chr11:69077161
|
A | ACCTGCCC others(12): Show |
1 | a0001c0005t0004g0024 | 2 | NA18990.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1231-1317_1231-129 others(23): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077161 | |||||
| chr11:69077176
|
G | A | 62 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(59): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1231-1306G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077176 | ||||||
| chr11:69077176
|
G | GTGTCCCT others(525): Show |
4 | a0001c0001t0003g0019a0001c0001t0003g0072a0001c0001t0003g0078others(1): Show | 4 | NA18956.hp2 NA18962.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-1299_1231-129 others(536): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077176 | |||||
| chr11:69077176
|
G | GTGTCCCT others(159): Show |
6 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(3): Show | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-1299_1231-129 others(170): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077176 | |||||
| chr11:69077176
|
G | GTGTCCCT others(159): Show |
4 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(1): Show | 6 | HG01346.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-1299_1231-129 others(170): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077176 | |||||
| chr11:69077184
|
T | C | 80 | a0001c0001t0003g0019a0001c0001t0003g0072a0001c0001t0003g0078others(77): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1231-1298T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077184 | ||||||
| chr11:69077184
|
T | TCACCTGC others(43): Show |
1 | a0003c0003t0002g0129 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1231-1280_1231-123 others(54): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077184 | |||||
| chr11:69077186
|
A | ACTTGCCC others(125): Show |
1 | a0002c0002t0001g0229 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1231-1295_1231-129 others(136): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077186 | |||||
| chr11:69077201
|
A | G | 18 | a0001c0001t0011g0293a0001c0001t0011g0294a0001c0005t0004g0097others(15): Show | 22 | HG01346.hp1 HG01515.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1231-1281A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077201 | ||||||
| chr11:69077202
|
T | C | 16 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(13): Show | 18 | HG01346.hp2 HG01891.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1231-1280T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077202 | ||||||
| chr11:69077209
|
C | T | 3 | a0001c0005t0004g0097a0005c0004t0007g0149a0023c0041t0004g0088 | 3 | HG02523.hp1 HG02717.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1231-1273C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077209 | ||||||
| chr11:69077211
|
A | ACCTGCCC others(1): Show |
16 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(13): Show | 18 | HG01346.hp2 HG01891.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1231-1264_1231-125 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077211 | |||||
| chr11:69077226
|
A | G | 6 | a0003c0003t0002g0034a0003c0003t0002g0035a0003c0003t0002g0126others(3): Show | 8 | HG01346.hp1 HG01515.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1231-1256A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077226 | ||||||
| chr11:69077227
|
T | C | 1 | a0004c0023t0019g0271 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1231-1255T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077227 | ||||||
| chr11:69077227
|
T | TGTCCCTC others(176): Show |
1 | a0004c0006t0020g0047 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1231-1245_1231-124 others(187): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077227 | |||||
| chr11:69077228
|
G | A | 1 | a0001c0001t0005g0274 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1231-1254G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077228 | ||||||
| chr11:69077234
|
C | T | 3 | a0003c0003t0002g0034a0003c0003t0002g0126a0003c0003t0002g0166 | 4 | HG01346.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1248C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077234 | ||||||
| chr11:69077246
|
C | T | 10 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(7): Show | 12 | HG01346.hp2 HG01891.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1231-1236C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077246 | ||||||
| chr11:69077251
|
A | G | 3 | a0004c0013t0015g0038a0004c0013t0015g0208a0004c0013t0015g0211 | 4 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1231A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077251 | ||||||
| chr11:69077252
|
C | T | 7 | a0001c0005t0004g0097a0003c0003t0002g0034a0003c0003t0002g0126others(4): Show | 9 | HG01346.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1231-1230C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077252 | ||||||
| chr11:69077253
|
G | A | 67 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(64): Show | 88 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1231-1229G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077253 | ||||||
| chr11:69077261
|
ACCTGCCC others(1): Show |
A | 25 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(22): Show | 37 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.1231-1206_1231-119 others(12): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077261 | |||||
| chr11:69077263
|
C | T | 3 | a0004c0013t0015g0038a0004c0013t0015g0208a0004c0013t0015g0211 | 4 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1219C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077263 | ||||||
| chr11:69077269
|
T | TCCTGCCA others(10): Show |
1 | a0023c0041t0004g0088 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1231-1207_1231-120 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077269 | |||||
| chr11:69077269
|
T | TCCTGCCA others(10): Show |
3 | a0003c0003t0002g0034a0003c0003t0002g0126a0003c0003t0002g0166 | 4 | HG01346.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1207_1231-120 others(21): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077269 | |||||
| chr11:69077269
|
T | TCCTGCCC others(267): Show |
1 | a0002c0002t0001g0229 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1231-1187_1231-118 others(278): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077269 | |||||
| chr11:69077269
|
T | TCCTGCCC others(243): Show |
1 | a0004c0013t0015g0209 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1231-1199_1231-119 others(254): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077269 | |||||
| chr11:69077269
|
T | TCCTGCCC others(95): Show |
1 | a0002c0002t0001g0230 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1231-1204_1231-120 others(106): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077269 | |||||
| chr11:69077269
|
T | TCCTGCCG others(260): Show |
3 | a0004c0013t0015g0038a0004c0013t0015g0208a0004c0013t0015g0211 | 4 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1207_1231-120 others(271): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077269 | |||||
| chr11:69077284
|
A | G | 4 | a0004c0013t0015g0038a0004c0013t0015g0208a0004c0013t0015g0209others(1): Show | 5 | HG02886.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-1198A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077284 | ||||||
| chr11:69077285
|
T | C | 1 | a0001c0005t0004g0097 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1231-1197T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077285 | ||||||
| chr11:69077292
|
C | CCACCTGC others(101): Show |
1 | a0004c0011t0012g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1231-1187_1231-118 others(112): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077292 | |||||
| chr11:69077296
|
T | C | 220 | a0001c0005t0004g0097a0002c0002t0001g0002a0002c0002t0001g0003others(217): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1231-1186T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077296 | ||||||
| chr11:69077309
|
G | A | 8 | a0001c0005t0004g0097a0004c0008t0013g0194a0004c0008t0013g0196others(5): Show | 8 | HG01884.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1231-1173G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077309 | ||||||
| chr11:69077317
|
C | T | 1 | a0004c0011t0012g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1231-1165C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077317 | ||||||
| chr11:69077321
|
C | T | 1 | a0001c0005t0004g0097 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1231-1161C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077321 | ||||||
| chr11:69077333
|
T | C | 109 | a0001c0001t0005g0296a0001c0005t0004g0097a0003c0003t0002g0009others(106): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1231-1149T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077333 | ||||||
| chr11:69077334
|
G | A | 2 | a0001c0001t0005g0296a0004c0011t0012g0201 | 2 | HG03195.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1231-1148G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077334 | ||||||
| chr11:69077342
|
T | C | 20 | a0001c0001t0005g0296a0001c0005t0004g0097a0001c0005t0042g0089others(17): Show | 21 | HG00639.hp1 HG01884.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1231-1140T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077342 | ||||||
| chr11:69077342
|
T | TCACCTGC others(19): Show |
1 | a0001c0001t0005g0287 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1231-1117_1231-111 others(30): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077342 | |||||
| chr11:69077342
|
T | TCACCTGC others(18): Show |
1 | a0004c0006t0033g0207 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1231-1123_1231-109 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077342 | |||||
| chr11:69077342
|
T | TCACCTGC others(18): Show |
1 | a0005c0004t0008g0151 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1231-1124_1231-112 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077342 | |||||
| chr11:69077342
|
T | TCACCTGC others(43): Show |
4 | a0004c0011t0012g0203a0004c0011t0012g0205a0004c0011t0012g0206others(1): Show | 4 | HG02080.hp2 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231-1124_1231-112 others(54): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077342 | |||||
| chr11:69077342
|
T | TCACCTGC others(68): Show |
3 | a0004c0011t0012g0204a0004c0011t0012g0210a0004c0031t0012g0202 | 3 | HG02809.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1231-1124_1231-112 others(79): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077342 | |||||
| chr11:69077358
|
C | T | 1 | a0001c0005t0004g0097 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1231-1124C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077358 | ||||||
| chr11:69077359
|
A | G | 1 | a0001c0005t0004g0097 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1231-1123A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077359 | ||||||
| chr11:69077360
|
T | TGTCCCTC others(18): Show |
6 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(3): Show | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077360 | |||||
| chr11:69077363
|
C | CCTCCACC others(90): Show |
1 | a0002c0002t0001g0249 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1231-1118_1231-111 others(101): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077363 | |||||
| chr11:69077371
|
C | CTGCCCTC others(93): Show |
10 | a0004c0008t0004g0105a0004c0008t0013g0194a0004c0008t0013g0196others(7): Show | 10 | HG01884.hp2 HG02258.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(104): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | |||||
| chr11:69077371
|
C | CTGCCCTC others(68): Show |
8 | a0001c0001t0005g0300a0004c0008t0017g0184a0004c0008t0034g0185others(5): Show | 8 | HG00099.hp2 HG00642.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(79): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | |||||
| chr11:69077371
|
C | CTGCCCTC others(43): Show |
113 | a0001c0001t0003g0064a0001c0001t0011g0170a0001c0001t0011g0291others(110): Show | 136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(54): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | |||||
| chr11:69077371
|
C | CTGCCCTC others(68): Show |
1 | a0003c0003t0002g0033 | 2 | NA19010.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(79): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | |||||
| chr11:69077371
|
C | CTGCCCTC others(143): Show |
1 | a0002c0002t0001g0232 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1231-1099_1231-109 others(154): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | |||||
| chr11:69077371
|
C | CTGCCCTC others(409): Show |
1 | a0001c0001t0003g0020 | 2 | NA18985.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(420): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | |||||
| chr11:69077371
|
C | CTGCCCTC others(93): Show |
64 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(61): Show | 85 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(104): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | |||||
| chr11:69077371
|
C | CTGCCCTC others(18): Show |
74 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(71): Show | 89 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(29): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | |||||
| chr11:69077371
|
C | CTGCCCTC others(392): Show |
3 | a0001c0001t0003g0021a0001c0001t0003g0066a0001c0001t0003g0067 | 4 | NA18986.hp1 NA18998.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1231-1099_1231-109 others(403): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69077371 | |||||
| chr11:69077371
|
C | T | 42 | a0001c0001t0003g0019a0001c0001t0003g0072a0001c0001t0003g0078others(39): Show | 59 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1231-1111C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077371 | ||||||
| chr11:69077474
|
G | T | 1 | a0003c0003t0002g0131 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1231-1008G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077474 | ||||||
| chr11:69077498
|
G | A | 254 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(251): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1231-984G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077498 | ||||||
| chr11:69077500
|
C | T | 1 | a0001c0005t0004g0097 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1231-982C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077500 | ||||||
| chr11:69077519
|
C | G | 7 | a0004c0008t0013g0194a0004c0008t0013g0196a0004c0008t0013g0197others(4): Show | 7 | HG01884.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1231-963C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077519 | ||||||
| chr11:69077647
|
A | G | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1231-835A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077647 | ||||||
| chr11:69077689
|
G | A | 6 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(3): Show | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231-793G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077689 | ||||||
| chr11:69077712
|
G | T | 1 | a0001c0001t0005g0292 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1231-770G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077712 | ||||||
| chr11:69077847
|
T | G | 1 | a0018c0022t0001g0240 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1231-635T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077847 | ||||||
| chr11:69077928
|
C | T | 1 | a0004c0023t0019g0271 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1231-554C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077928 | ||||||
| chr11:69077974
|
A | G | 219 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(216): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1231-508A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69077974 | ||||||
| chr11:69078050
|
C | T | 1 | a0001c0001t0010g0309 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1231-432C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69078050 | ||||||
| chr11:69078159
|
C | CT | 87 | a0001c0001t0003g0077a0001c0001t0011g0294a0003c0003t0002g0009others(84): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.1231-310dupT | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr11 | 69078159 | |||||
| chr11:69078199
|
A | C | 1 | a0004c0006t0033g0207 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1231-283A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69078199 | ||||||
| chr11:69078268
|
A | G | 1 | a0003c0003t0039g0127 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1231-214A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69078268 | ||||||
| chr11:69078395
|
C | T | 1 | a0003c0003t0002g0034 | 2 | HG01346.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1231-87C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69078395 | ||||||
| chr11:69078399
|
G | A | 84 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(81): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1231-83G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 13/24 | chr11 | 69078399 | ||||||
| chr11:69078630
|
A | G | 219 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(216): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1350+29A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 14/24 | chr11 | 69078630 | ||||||
| chr11:69079051
|
A | C | 280 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(277): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1539+31A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079051 | ||||||
| chr11:69079069
|
C | T | 7 | a0004c0011t0012g0201a0004c0011t0012g0203a0004c0011t0012g0204others(4): Show | 7 | HG02809.hp1 HG02895.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1539+49C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079069 | ||||||
| chr11:69079110
|
G | A | 2 | a0003c0003t0002g0013a0003c0003t0002g0119 | 4 | HG01074.hp2 HG01243.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1539+90G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079110 | ||||||
| chr11:69079418
|
T | C | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1539+398T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079418 | ||||||
| chr11:69079537
|
A | G | 280 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(277): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1540-297A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079537 | ||||||
| chr11:69079582
|
C | T | 1 | a0002c0002t0001g0243 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1540-252C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079582 | ||||||
| chr11:69079628
|
C | T | 1 | a0001c0005t0004g0056 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1540-206C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079628 | ||||||
| chr11:69079670
|
T | C | 219 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(216): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1540-164T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079670 | ||||||
| chr11:69079688
|
C | T | 82 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(79): Show | 103 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1540-146C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 16/24 | chr11 | 69079688 | ||||||
| chr11:69080219
|
C | G | 35 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(32): Show | 45 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1589+336C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080219 | ||||||
| chr11:69080353
|
A | T | 21 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(18): Show | 23 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.1589+470A>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080353 | ||||||
| chr11:69080498
|
G | T | 7 | a0003c0003t0002g0031a0003c0003t0002g0113a0003c0003t0002g0120others(4): Show | 8 | HG00558.hp1 NA18973.hp2 NA19011.hp2 others(5): Show |
intron_variant | MODIFIER | c.1589+615G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080498 | ||||||
| chr11:69080499
|
C | T | 7 | a0003c0003t0002g0031a0003c0003t0002g0113a0003c0003t0002g0120others(4): Show | 8 | HG00558.hp1 NA18973.hp2 NA19011.hp2 others(5): Show |
intron_variant | MODIFIER | c.1589+616C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080499 | ||||||
| chr11:69080520
|
G | A | 1 | a0003c0003t0002g0113 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1589+637G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080520 | ||||||
| chr11:69080561
|
C | T | 2 | a0004c0006t0019g0270a0004c0006t0020g0047 | 3 | HG02145.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1589+678C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080561 | ||||||
| chr11:69080606
|
T | C | 1 | a0004c0008t0017g0184 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1589+723T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080606 | ||||||
| chr11:69080665
|
T | G | 1 | a0001c0001t0003g0069 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1590-735T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080665 | ||||||
| chr11:69080764
|
C | T | 1 | a0001c0001t0011g0293 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1590-636C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080764 | ||||||
| chr11:69080918
|
C | T | 21 | a0006c0007t0006g0004a0006c0007t0006g0168a0006c0007t0006g0169others(18): Show | 26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1590-482C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69080918 | ||||||
| chr11:69081004
|
C | T | 1 | a0006c0007t0021g0036 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1590-396C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69081004 | ||||||
| chr11:69081136
|
C | T | 1 | a0007c0009t0004g0093 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1590-264C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69081136 | ||||||
| chr11:69081144
|
A | G | 219 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(216): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1590-256A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69081144 | ||||||
| chr11:69081281
|
A | G | 2 | a0004c0008t0004g0105a0004c0008t0017g0183 | 2 | HG02258.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1590-119A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69081281 | ||||||
| chr11:69081317
|
G | A | 1 | a0007c0009t0004g0086 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1590-83G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69081317 | ||||||
| chr11:69081368
|
C | T | 3 | a0004c0011t0012g0203a0004c0011t0012g0205a0004c0011t0012g0210 | 3 | HG02965.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1590-32C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 17/24 | chr11 | 69081368 | ||||||
| chr11:69081592
|
G | A | 6 | a0001c0001t0004g0290a0001c0001t0011g0170a0001c0001t0011g0291others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689+93G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081592 | ||||||
| chr11:69081605
|
G | A | 84 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(81): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1689+106G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081605 | ||||||
| chr11:69081644
|
C | T | 2 | a0004c0008t0013g0196a0004c0008t0013g0197 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1689+145C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081644 | ||||||
| chr11:69081670
|
T | G | 1 | a0004c0006t0007g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1689+171T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081670 | ||||||
| chr11:69081722
|
C | T | 1 | a0003c0003t0002g0108 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1689+223C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081722 | ||||||
| chr11:69081816
|
G | C | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1689+317G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081816 | ||||||
| chr11:69081852
|
C | T | 1 | a0003c0003t0002g0107 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1689+353C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081852 | ||||||
| chr11:69081874
|
T | C | 220 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(217): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1689+375T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081874 | ||||||
| chr11:69081936
|
C | T | 36 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(33): Show | 46 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1689+437C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69081936 | ||||||
| chr11:69082010
|
G | A | 4 | a0001c0001t0005g0011a0001c0001t0005g0292a0001c0001t0005g0295others(1): Show | 7 | NA18942.hp1 NA18945.hp2 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1689+511G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082010 | ||||||
| chr11:69082133
|
G | A | 2 | a0003c0003t0002g0130a0003c0003t0002g0131 | 2 | HG00738.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1689+634G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082133 | ||||||
| chr11:69082177
|
G | A | 1 | a0002c0002t0001g0266 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1689+678G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082177 | ||||||
| chr11:69082218
|
C | T | 1 | a0004c0006t0018g0015 | 3 | NA19009.hp2 NA19065.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1689+719C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082218 | ||||||
| chr11:69082246
|
A | G | 324 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(321): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1689+747A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082246 | ||||||
| chr11:69082350
|
A | G | 1 | a0015c0037t0001g0237 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1689+851A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082350 | ||||||
| chr11:69082360
|
A | G | 1 | a0001c0001t0004g0290 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1689+861A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082360 | ||||||
| chr11:69082377
|
A | G | 22 | a0002c0002t0001g0236a0006c0007t0006g0004a0006c0007t0006g0168others(19): Show | 27 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1689+878A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082377 | ||||||
| chr11:69082501
|
C | T | 1 | a0003c0003t0002g0120 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1689+1002C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082501 | ||||||
| chr11:69082525
|
G | A | 2 | a0003c0003t0002g0124a0003c0003t0002g0132 | 2 | NA18959.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1689+1026G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082525 | ||||||
| chr11:69082556
|
GGTAAGAC others(117): Show |
G | 1 | a0023c0041t0004g0088 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1689+1090_1689+121 others(4): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr11 | 69082556 | |||||
| chr11:69082564
|
G | T | 1 | a0005c0004t0007g0149 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1689+1065G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082564 | ||||||
| chr11:69082572
|
G | A | 2 | a0005c0004t0007g0141a0005c0004t0007g0147 | 2 | HG01081.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1689+1073G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082572 | ||||||
| chr11:69082589
|
A | C | 3 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0023t0019g0271 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689+1090A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082589 | ||||||
| chr11:69082618
|
GGTAAGAC others(55): Show |
G | 181 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(178): Show | 230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1690-1172_1690-111 others(66): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr11 | 69082618 | |||||
| chr11:69082651
|
G | A | 91 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(88): Show | 116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1689+1152G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082651 | ||||||
| chr11:69082680
|
T | G | 91 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(88): Show | 116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.1689+1181T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082680 | ||||||
| chr11:69082695
|
C | T | 1 | a0003c0003t0002g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1689+1196C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082695 | ||||||
| chr11:69082708
|
A | G | 1 | a0020c0024t0007g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1689+1209A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082708 | ||||||
| chr11:69082713
|
G | A | 1 | a0003c0003t0002g0121 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1689+1214G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082713 | ||||||
| chr11:69082734
|
C | T | 1 | a0003c0003t0002g0144 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1690-1211C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082734 | ||||||
| chr11:69082742
|
T | G | 8 | a0003c0003t0002g0144a0004c0015t0014g0051a0004c0015t0014g0052others(5): Show | 8 | HG00423.hp2 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690-1203T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082742 | ||||||
| chr11:69082749
|
C | T | 4 | a0004c0006t0009g0016a0004c0006t0009g0190a0004c0006t0009g0192others(1): Show | 6 | HG01346.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-1196C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082749 | ||||||
| chr11:69082763
|
T | C | 7 | a0002c0002t0001g0233a0004c0015t0014g0051a0004c0015t0014g0052others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1690-1182T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082763 | ||||||
| chr11:69082773
|
G | A | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-1172G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082773 | ||||||
| chr11:69082773
|
GCGTGCAG others(55): Show |
G | 1 | a0003c0003t0002g0144 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1690-1141_1690-108 others(66): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr11 | 69082773 | |||||
| chr11:69082775
|
G | A | 7 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(4): Show | 7 | HG02572.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1690-1170G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082775 | ||||||
| chr11:69082796
|
C | G | 1 | a0004c0011t0012g0206 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1690-1149C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082796 | ||||||
| chr11:69082796
|
C | T | 108 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(105): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1690-1149C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082796 | ||||||
| chr11:69082804
|
T | G | 219 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(216): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1690-1141T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082804 | ||||||
| chr11:69082805
|
G | A | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-1140G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082805 | ||||||
| chr11:69082812
|
G | T | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-1133G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082812 | ||||||
| chr11:69082825
|
T | C | 104 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(101): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1690-1120T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082825 | ||||||
| chr11:69082835
|
A | G | 105 | a0001c0001t0004g0290a0001c0001t0011g0170a0001c0001t0011g0291others(102): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1690-1110A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082835 | ||||||
| chr11:69082837
|
G | A | 8 | a0001c0001t0005g0274a0001c0001t0005g0277a0001c0001t0005g0278others(5): Show | 8 | HG00544.hp2 HG01496.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690-1108G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082837 | ||||||
| chr11:69082850
|
T | C | 10 | a0002c0002t0001g0044a0002c0002t0001g0045a0002c0002t0001g0254others(7): Show | 12 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.1690-1095T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082850 | ||||||
| chr11:69082858
|
C | T | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1690-1087C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082858 | ||||||
| chr11:69082866
|
G | T | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-1079G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082866 | ||||||
| chr11:69082867
|
A | G | 7 | a0001c0001t0010g0307a0004c0015t0014g0051a0004c0015t0014g0052others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1690-1078A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082867 | ||||||
| chr11:69082873
|
C | T | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-1072C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082873 | ||||||
| chr11:69082874
|
G | T | 104 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(101): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1690-1071G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082874 | ||||||
| chr11:69082874
|
GCATGATC others(179): Show |
G | 3 | a0001c0001t0005g0011a0001c0001t0005g0295a0001c0001t0005g0296 | 6 | NA18942.hp1 NA18945.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-1046_1690-861 others(3): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr11 | 69082874 | |||||
| chr11:69082899
|
G | A | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1690-1046G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082899 | ||||||
| chr11:69082912
|
C | T | 42 | a0001c0001t0004g0290a0001c0001t0005g0048a0001c0001t0005g0272others(39): Show | 44 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1690-1033C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082912 | ||||||
| chr11:69082922
|
T | C | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1690-1023T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082922 | ||||||
| chr11:69082935
|
TGCATGAT others(55): Show |
T | 1 | a0004c0008t0017g0183 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1690-947_1690-886d others(64): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr11 | 69082935 | |||||
| chr11:69082961
|
A | G | 1 | a0001c0001t0003g0070 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1690-984A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082961 | ||||||
| chr11:69082982
|
C | T | 1 | a0016c0036t0001g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1690-963C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69082982 | ||||||
| chr11:69082998
|
GCATGATC others(55): Show |
G | 25 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(22): Show | 37 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.1690-910_1690-849d others(64): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr11 | 69082998 | |||||
| chr11:69083060
|
A | G | 1 | a0006c0007t0006g0177 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1690-885A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083060 | ||||||
| chr11:69083082
|
C | T | 1 | a0002c0002t0001g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1690-863C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083082 | ||||||
| chr11:69083096
|
C | T | 2 | a0004c0011t0012g0205a0004c0011t0012g0210 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1690-849C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083096 | ||||||
| chr11:69083141
|
C | T | 7 | a0001c0001t0003g0022a0001c0001t0003g0055a0001c0001t0003g0063others(4): Show | 8 | HG00408.hp1 HG00609.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.1690-804C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083141 | ||||||
| chr11:69083305
|
G | C | 21 | a0006c0007t0006g0004a0006c0007t0006g0168a0006c0007t0006g0169others(18): Show | 26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1690-640G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083305 | ||||||
| chr11:69083347
|
G | A | 3 | a0004c0006t0019g0270a0004c0006t0020g0047a0004c0023t0019g0271 | 4 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1690-598G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083347 | ||||||
| chr11:69083650
|
C | T | 1 | a0003c0003t0002g0030 | 2 | NA18954.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1690-295C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083650 | ||||||
| chr11:69083670
|
C | T | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1690-275C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083670 | ||||||
| chr11:69083703
|
G | A | 6 | a0004c0015t0014g0051a0004c0015t0014g0052a0004c0015t0014g0053others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690-242G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083703 | ||||||
| chr11:69083768
|
T | A | 1 | a0002c0002t0001g0236 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1690-177T>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083768 | ||||||
| chr11:69083873
|
G | T | 1 | a0008c0010t0006g0103 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1690-72G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 18/24 | chr11 | 69083873 | ||||||
| chr11:69084079
|
G | A | 21 | a0006c0007t0006g0004a0006c0007t0006g0168a0006c0007t0006g0169others(18): Show | 26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1761+63G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084079 | ||||||
| chr11:69084125
|
C | G | 4 | a0001c0001t0005g0286a0001c0001t0005g0287a0001c0001t0005g0288others(1): Show | 4 | NA18612.hp1 NA18947.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1761+109C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084125 | ||||||
| chr11:69084137
|
C | T | 84 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(81): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1761+121C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084137 | ||||||
| chr11:69084238
|
G | C | 2 | a0001c0001t0022g0302a0001c0001t0022g0303 | 2 | HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1761+222G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084238 | ||||||
| chr11:69084322
|
G | A | 1 | a0001c0001t0005g0304 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1761+306G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084322 | ||||||
| chr11:69084438
|
A | G | 1 | a0005c0004t0007g0141 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1761+422A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084438 | ||||||
| chr11:69084589
|
G | A | 84 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(81): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1761+573G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084589 | ||||||
| chr11:69084613
|
G | C | 1 | a0006c0007t0006g0178 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1761+597G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084613 | ||||||
| chr11:69084630
|
C | T | 24 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(21): Show | 36 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1762-580C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084630 | ||||||
| chr11:69084647
|
G | A | 1 | a0002c0002t0001g0041 | 2 | HG02071.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1762-563G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084647 | ||||||
| chr11:69084713
|
C | T | 83 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(80): Show | 104 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1762-497C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084713 | ||||||
| chr11:69084748
|
C | G | 4 | a0004c0008t0004g0105a0004c0008t0017g0106a0004c0008t0017g0183others(1): Show | 4 | HG02258.hp2 HG02630.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1762-462C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084748 | ||||||
| chr11:69084847
|
G | A | 110 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1762-363G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084847 | ||||||
| chr11:69084854
|
G | A | 1 | a0001c0001t0003g0061 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1762-356G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084854 | ||||||
| chr11:69084868
|
T | C | 21 | a0006c0007t0006g0004a0006c0007t0006g0168a0006c0007t0006g0169others(18): Show | 26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1762-342T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084868 | ||||||
| chr11:69084890
|
C | T | 21 | a0006c0007t0006g0004a0006c0007t0006g0168a0006c0007t0006g0169others(18): Show | 26 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1762-320C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69084890 | ||||||
| chr11:69085029
|
G | A | 21 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(18): Show | 23 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.1762-181G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69085029 | ||||||
| chr11:69085176
|
G | A | 6 | a0004c0006t0009g0213a0004c0006t0009g0214a0004c0006t0009g0215others(3): Show | 6 | HG02572.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1762-34G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69085176 | ||||||
| chr11:69085192
|
C | T | 33 | a0001c0001t0005g0011a0001c0001t0005g0048a0001c0001t0005g0272others(30): Show | 37 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1762-18C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 19/24 | chr11 | 69085192 | ||||||
| chr11:69085338
|
G | A | 1 | a0005c0004t0008g0122 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1838+52G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 20/24 | chr11 | 69085338 | ||||||
| chr11:69085460
|
C | T | 1 | a0005c0004t0007g0269 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1838+174C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 20/24 | chr11 | 69085460 | ||||||
| chr11:69085550
|
C | T | 1 | a0003c0003t0002g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1839-121C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 20/24 | chr11 | 69085550 | ||||||
| chr11:69085565
|
T | G | 220 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(217): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1839-106T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 20/24 | chr11 | 69085565 | ||||||
| chr11:69085616
|
C | A | 2 | a0003c0003t0002g0112a0003c0003t0002g0117 | 2 | HG01257.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1839-55C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 20/24 | chr11 | 69085616 | ||||||
| chr11:69085640
|
G | A | 1 | a0002c0002t0001g0234 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1839-31G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 20/24 | chr11 | 69085640 | ||||||
| chr11:69085774
|
AGCACCCT others(3): Show |
A | 1 | a0002c0002t0001g0227 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1920+23_1920+32del others(10): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 21/24 | chr11 | 69085774 | ||||||
| chr11:69085964
|
C | T | 1 | a0022c0028t0040g0242 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2003+34C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/24 | chr11 | 69085964 | ||||||
| chr11:69085993
|
G | A | 1 | a0004c0008t0031g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2003+63G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/24 | chr11 | 69085993 | ||||||
| chr11:69086036
|
C | T | 97 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(94): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.2003+106C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/24 | chr11 | 69086036 | ||||||
| chr11:69086064
|
G | A | 22 | a0001c0001t0004g0290a0004c0006t0009g0213a0004c0006t0009g0214others(19): Show | 24 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(21): Show |
intron_variant | MODIFIER | c.2003+134G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/24 | chr11 | 69086064 | ||||||
| chr11:69086219
|
G | A | 8 | a0002c0027t0001g0186a0004c0015t0014g0051a0004c0015t0014g0052others(5): Show | 8 | HG02451.hp1 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2003+289G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/24 | chr11 | 69086219 | ||||||
| chr11:69086309
|
C | T | 1 | a0010c0014t0013g0198 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2004-214C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/24 | chr11 | 69086309 | ||||||
| chr11:69086381
|
T | C | 2 | a0002c0027t0001g0186a0016c0036t0001g0187 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2004-142T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 22/24 | chr11 | 69086381 | ||||||
| chr11:69086623
|
C | G | 1 | a0001c0001t0005g0300 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2085+19C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69086623 | ||||||
| chr11:69086662
|
C | T | 1 | a0002c0002t0001g0262 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2085+58C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69086662 | ||||||
| chr11:69086714
|
C | A | 1 | a0005c0004t0007g0026 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2085+110C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69086714 | ||||||
| chr11:69086794
|
T | C | 1 | a0004c0006t0033g0207 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2085+190T>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69086794 | ||||||
| chr11:69086800
|
A | AGTGCTCC others(29): Show |
4 | a0001c0001t0005g0011a0001c0001t0005g0292a0001c0001t0005g0295others(1): Show | 7 | NA18942.hp1 NA18945.hp2 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.2085+254_2086-219d others(38): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr11 | 69086800 | |||||
| chr11:69086800
|
A | G | 1 | a0023c0041t0004g0088 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2085+196A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69086800 | ||||||
| chr11:69086800
|
AGTGCTCC others(29): Show |
A | 2 | a0004c0006t0033g0207a0006c0007t0006g0178 | 2 | HG02155.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2085+254_2086-219d others(38): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr11 | 69086800 | |||||
| chr11:69086833
|
G | GGGGGTGC others(29): Show |
277 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(274): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.2086-244_2086-243i others(38): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr11 | 69086833 | |||||
| chr11:69086833
|
G | GGGGGTGC others(101): Show |
3 | a0003c0003t0002g0029a0003c0003t0002g0121a0003c0003t0002g0123 | 4 | NA18940.hp1 NA18990.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.2086-244_2086-243i others(110): Show |
TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr11 | 69086833 | |||||
| chr11:69086833
|
G | T | 1 | a0023c0041t0004g0088 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2085+229G>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69086833 | ||||||
| chr11:69086980
|
C | T | 3 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157 | 3 | HG00438.hp2 NA18945.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.2086-132C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69086980 | ||||||
| chr11:69087032
|
G | A | 1 | a0001c0001t0004g0290 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2086-80G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69087032 | ||||||
| chr11:69087076
|
G | C | 27 | a0001c0001t0005g0048a0001c0001t0005g0277a0001c0001t0005g0279others(24): Show | 28 | HG00558.hp2 HG00597.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.2086-36G>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69087076 | ||||||
| chr11:69087087
|
A | G | 1 | a0002c0002t0001g0244 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2086-25A>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 23/24 | chr11 | 69087087 | ||||||
| chr11:69087284
|
C | T | 1 | a0002c0002t0001g0223 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2180+78C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087284 | ||||||
| chr11:69087287
|
C | T | 1 | a0002c0002t0001g0276 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2180+81C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087287 | ||||||
| chr11:69087368
|
C | T | 1 | a0004c0006t0036g0218 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2180+162C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087368 | ||||||
| chr11:69087510
|
A | C | 323 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0012others(320): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.2180+304A>C | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087510 | ||||||
| chr11:69087625
|
G | A | 2 | a0005c0004t0008g0109a0005c0004t0008g0140 | 2 | NA18946.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.2181-250G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087625 | ||||||
| chr11:69087644
|
C | T | 19 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(16): Show | 28 | HG00423.hp1 HG00438.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.2181-231C>T | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087644 | ||||||
| chr11:69087729
|
T | G | 112 | a0002c0002t0001g0002a0002c0002t0001g0003a0002c0002t0001g0005others(109): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.2181-146T>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087729 | ||||||
| chr11:69087765
|
G | A | 114 | a0003c0003t0002g0009a0003c0003t0002g0013a0003c0003t0002g0014others(111): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.2181-110G>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087765 | ||||||
| chr11:69087846
|
C | A | 2 | a0004c0016t0014g0049a0004c0016t0014g0050 | 2 | HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2181-29C>A | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087846 | ||||||
| chr11:69087864
|
C | G | 6 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(3): Show | 6 | HG00544.hp2 HG01928.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.2181-11C>G | TPCN2 | ENSG00000162341.18 | transcript | ENST00000294309.8 | protein_coding | 24/24 | chr11 | 69087864 |