Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 57157 |
|---|---|
| ensemblid | ENSG00000006576.17 |
| hgncid | 13411 |
| symbol | PHTF2 |
| name | putative homeodomain transcription factor 2 |
| refseq_nuc | NM_001395272.1 |
| refseq_prot | NP_001382201.1 |
| ensembl_nuc | ENST00000422959.8 |
| ensembl_prot | ENSP00000403042.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 77798773 |
| end | 77957225 |
| strand | + |
| ver | v1.2 |
| region | chr7:77798773-77957225 |
| region5000 | chr7:77793773-77962225 |
| regionname0 | PHTF2_chr7_77798773_77957225 |
| regionname5000 | PHTF2_chr7_77793773_77962225 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 751 | 310 | 87 | 60 | 112 | 12 | 37 | 84 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0002 | 0/0 | 751 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0003 | 0/0 | 751 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0004 | 0/0 | 751 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2256 | 243 | 70 | 47 | 91 | 9 | 24 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| c0002 | 0/0 | 2256 | 57 | 13 | 11 | 20 | 1 | 12 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| c0003 | 0/0 | 2256 | 5 | 0 | 2 | 0 | 2 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| c0004 | 0/0 | 2256 | 3 | 3 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| c0005 | 0/0 | 2256 | 2 | 0 | 0 | 0 | 2 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| c0006 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| c0007 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| c0008 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| c0009 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2582 | 221 | 52 | 45 | 89 | 10 | 23 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0002 | 0/0 | 2582 | 51 | 9 | 10 | 20 | 1 | 11 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0003 | 0/0 | 2582 | 6 | 6 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0004 | 0/0 | 2582 | 5 | 0 | 2 | 0 | 2 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0005 | 0/0 | 2584 | 4 | 3 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0006 | 0/0 | 2582 | 3 | 3 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0007 | 0/0 | 2582 | 3 | 3 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0008 | 0/0 | 2582 | 2 | 0 | 0 | 2 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0009 | 0/0 | 2582 | 2 | 1 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0010 | 0/0 | 2582 | 2 | 2 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0011 | 0/0 | 2582 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0012 | 0/0 | 2582 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0013 | 0/0 | 2582 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0014 | 0/0 | 2582 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0015 | 0/0 | 2582 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0016 | 0/0 | 2582 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0017 | 0/0 | 2582 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0018 | 0/0 | 2582 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0019 | 0/0 | 2582 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0020 | 0/0 | 2582 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0021 | 0/0 | 2582 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0022 | 0/0 | 2582 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0023 | 0/0 | 2582 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0024 | 0/0 | 2582 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| t0025 | 0/0 | 2582 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0109 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0224 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2256 | 243 | 70 | 47 | 91 | 9 | 24 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0002 | 0/0 | 2256 | 57 | 13 | 11 | 20 | 1 | 12 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0003 | 0/0 | 2256 | 5 | 0 | 2 | 0 | 2 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0004 | 0/0 | 2256 | 3 | 3 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0006 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0009 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0002c0005 | 0/0 | 2256 | 2 | 0 | 0 | 0 | 2 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0003c0008 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0004c0007 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4837 | 215 | 50 | 45 | 88 | 8 | 22 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0001t0003 | 0/0 | 4837 | 6 | 6 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0001t0005 | 0/0 | 4839 | 4 | 3 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0001t0006 | 0/0 | 4837 | 3 | 3 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0001t0008 | 0/0 | 4837 | 2 | 0 | 0 | 2 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0001t0009 | 0/0 | 4837 | 2 | 1 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0001t0010 | 0/0 | 4837 | 2 | 2 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0001t0011 | 0/0 | 4837 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0001t0012 | 0/0 | 4837 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0001t0014 | 0/0 | 4837 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0001t0015 | 0/0 | 4837 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0001t0017 | 0/0 | 4837 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0001t0018 | 0/0 | 4837 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0001t0019 | 0/0 | 4837 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0001t0021 | 0/0 | 4837 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0001t0023 | 0/0 | 4837 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0002t0001 | 0/0 | 4837 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0002t0002 | 0/0 | 4837 | 51 | 9 | 10 | 20 | 1 | 11 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0002t0013 | 0/0 | 4837 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0002t0016 | 0/0 | 4837 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0002t0020 | 0/0 | 4837 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0002t0022 | 0/0 | 4837 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0002t0025 | 0/0 | 4837 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0003t0004 | 0/0 | 4837 | 5 | 0 | 2 | 0 | 2 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0004t0007 | 0/0 | 4837 | 3 | 3 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0006t0001 | 0/0 | 4837 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0001c0009t0001 | 0/0 | 4837 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0002c0005t0001 | 0/0 | 4837 | 2 | 0 | 0 | 0 | 2 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0003c0008t0024 | 0/0 | 4837 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| a0004c0007t0001 | 0/0 | 4837 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | copy fasta | chr7 | 77793773 | 77962225 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0109 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0224 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0006g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0008g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0008g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0009g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0010g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0011g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0012g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0014g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0015g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0017g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0018g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0019g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0021g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0001t0023g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0013g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0016g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0020g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0022g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0002t0025g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0003t0004g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0003t0004g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0003t0004g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0003t0004g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0003t0004g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0004t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0004t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0004t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0006t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0001c0009t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0002c0005t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0002c0005t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0003c0008t0024g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| a0004c0007t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | GBR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00140 | hp1 | a0001 | c0003 | t0004 | g0004 | EUR | GBR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | GBR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | FIN | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00280 | hp2 | a0002 | c0005 | t0001 | g0190 | EUR | FIN | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | FIN | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00323 | hp2 | a0002 | c0005 | t0001 | g0189 | EUR | FIN | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00438 | hp1 | a0001 | c0001 | t0008 | g0124 | EAS | CHS | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0043 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00642 | hp1 | a0001 | c0003 | t0004 | g0003 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0097 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0055 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0216 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01099 | hp1 | a0001 | c0002 | t0013 | g0294 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0304 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0176 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01256 | hp1 | a0001 | c0003 | t0004 | g0006 | AMR | CLM | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0217 | AMR | CLM | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01517 | hp2 | a0001 | c0001 | t0018 | g0160 | EUR | IBS | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01891 | hp1 | a0001 | c0002 | t0022 | g0080 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02015 | hp1 | a0001 | c0001 | t0008 | g0145 | EAS | KHV | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0310 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | KHV | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | KHV | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | KHV | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CDX | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CDX | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02257 | hp1 | a0001 | c0001 | t0014 | g0150 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02257 | hp2 | a0001 | c0001 | t0017 | g0071 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02258 | hp1 | a0001 | c0001 | t0011 | g0285 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0073 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02280 | hp1 | a0001 | c0001 | t0023 | g0278 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PEL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02451 | hp1 | a0003 | c0008 | t0024 | g0001 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02572 | hp1 | a0001 | c0004 | t0007 | g0069 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0177 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0307 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02723 | hp2 | a0001 | c0006 | t0001 | g0275 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0308 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02965 | hp1 | a0001 | c0004 | t0007 | g0017 | AFR | ESN | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0058 | AFR | ESN | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0311 | AFR | ESN | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | ESN | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0032 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0288 | AFR | ESN | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03209 | hp1 | a0001 | c0001 | t0021 | g0312 | AFR | MSL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0070 | AFR | MSL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03239 | hp2 | a0001 | c0003 | t0004 | g0002 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03453 | hp1 | a0001 | c0004 | t0007 | g0277 | AFR | MSL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | MSL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0215 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0050 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0049 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0289 | AFR | ESN | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0296 | AFR | MSL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03579 | hp2 | a0001 | c0002 | t0020 | g0293 | AFR | MSL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03669 | hp1 | a0001 | c0001 | t0019 | g0066 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0047 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03710 | hp2 | a0004 | c0007 | t0001 | g0110 | SAS | PJL | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03831 | hp2 | a0001 | c0002 | t0025 | g0060 | SAS | BEB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0067 | SAS | BEB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0068 | SAS | BEB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0059 | SAS | STU | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0046 | SAS | STU | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | STU | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0065 | SAS | STU | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | YRI | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0265 | AFR | YRI | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | CHB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0300 | AFR | YRI | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0048 | AFR | YRI | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18970 | hp2 | a0001 | c0001 | t0012 | g0303 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0306 | AFR | LWK | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | LWK | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | LWK | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | LWK | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19079 | hp1 | a0001 | c0009 | t0001 | g0079 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0072 | AFR | YRI | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0061 | AFR | ASW | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0085 | AFR | ASW | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0039 | EUR | TSI | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA20805 | hp1 | a0001 | c0003 | t0004 | g0005 | EUR | TSI | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | TSI | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA20905 | hp1 | a0001 | c0001 | t0015 | g0113 | SAS | GIH | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0098 | SAS | GIH | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0036 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG02559 | hp2 | a0001 | c0002 | t0016 | g0290 | AFR | ACB | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | USA | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | USA | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | USA | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | USA | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0309 | AFR | LWK | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | LWK | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0224 | REF | REF | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0109 | REF | REF | PHTF2_chr7_77793773_77962225 | PHTF2 | chr7 | 77793773 | 77962225 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77922720
|
C | G | 1 | a0003 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.959C>G | p.Ser320Cys | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/19 | 1193/4837 | 959/2256 | 320/751 | chr7 | 77922720 | ||
| chr7:77922741
|
G | A | 1 | a0002 | 2 | HG00280.hp2 HG00323.hp2 |
missense_variant | MODERATE | c.980G>A | p.Arg327Lys | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/19 | 1214/4837 | 980/2256 | 327/751 | chr7 | 77922741 | ||
| chr7:77942757
|
A | G | 1 | a0004 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.1828A>G | p.Ile610Val | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/19 | 2062/4837 | 1828/2256 | 610/751 | chr7 | 77942757 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77901796
|
T | C | 2 | a0001c0002a0001c0004 | 60 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(57): Show |
synonymous_variant | LOW | c.219T>C | p.Pro73Pro | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/19 | 453/4837 | 219/2256 | 73/751 | chr7 | 77901796 | ||
| chr7:77910308
|
T | C | 1 | a0001c0006 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.573T>C | p.Asp191Asp | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/19 | 807/4837 | 573/2256 | 191/751 | chr7 | 77910308 | ||
| chr7:77910356
|
C | T | 1 | a0001c0009 | 1 | NA19079.hp1 | synonymous_variant | LOW | c.621C>T | p.His207His | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/19 | 855/4837 | 621/2256 | 207/751 | chr7 | 77910356 | ||
| chr7:77940242
|
C | T | 1 | a0001c0003 | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
synonymous_variant | LOW | c.1578C>T | p.Arg526Arg | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 13/19 | 1812/4837 | 1578/2256 | 526/751 | chr7 | 77940242 | ||
| chr7:77949747
|
T | C | 1 | a0001c0004 | 3 | HG02572.hp1 HG02965.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.1927T>C | p.Leu643Leu | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/19 | 2161/4837 | 1927/2256 | 643/751 | chr7 | 77949747 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77798798
|
T | C | 1 | a0001c0001t0011 | 1 | HG02258.hp1 | 5_prime_UTR_variant | MODIFIER | c.-209T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/19 | 41458 | chr7 | 77798798 | |||||
| chr7:77798901
|
G | A | 1 | a0001c0001t0008 | 2 | HG00438.hp1 HG02015.hp1 |
5_prime_UTR_variant | MODIFIER | c.-106G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/19 | 41355 | chr7 | 77798901 | |||||
| chr7:77798960
|
C | T | 1 | a0001c0002t0025 | 1 | HG03831.hp2 | 5_prime_UTR_variant | MODIFIER | c.-47C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/19 | 41296 | chr7 | 77798960 | |||||
| chr7:77955024
|
T | C | 1 | a0001c0001t0012 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*146T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 146 | chr7 | 77955024 | |||||
| chr7:77955086
|
G | C | 1 | a0001c0002t0013 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*208G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 208 | chr7 | 77955086 | |||||
| chr7:77955152
|
T | G | 1 | a0001c0001t0014 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*274T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 274 | chr7 | 77955152 | |||||
| chr7:77955190
|
A | G | 1 | a0003c0008t0024 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*312A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 312 | chr7 | 77955190 | |||||
| chr7:77955239
|
C | T | 1 | a0001c0001t0023 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*361C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 361 | chr7 | 77955239 | |||||
| chr7:77955537
|
T | C | 1 | a0001c0001t0015 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*659T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 659 | chr7 | 77955537 | |||||
| chr7:77955572
|
A | G | 1 | a0001c0003t0004 | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*694A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 694 | chr7 | 77955572 | |||||
| chr7:77955606
|
T | A | 1 | a0001c0001t0006 | 3 | HG03579.hp1 NA18522.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*728T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 728 | chr7 | 77955606 | |||||
| chr7:77955607
|
G | A | 1 | a0001c0001t0009 | 2 | HG01243.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*729G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 729 | chr7 | 77955607 | |||||
| chr7:77955620
|
C | T | 1 | a0003c0008t0024 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*742C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 742 | chr7 | 77955620 | |||||
| chr7:77955665
|
G | C | 1 | a0001c0002t0016 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*787G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 787 | chr7 | 77955665 | |||||
| chr7:77955678
|
G | T | 3 | a0001c0002t0002a0001c0002t0022a0001c0002t0025 | 53 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*800G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 800 | chr7 | 77955678 | |||||
| chr7:77955720
|
T | TCC | 1 | a0001c0001t0005 | 4 | HG01109.hp2 HG02630.hp2 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*842_*843insCC | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 843 | chr7 | 77955720 | |||||
| chr7:77956047
|
A | T | 2 | a0001c0001t0003a0001c0001t0021 | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1169A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 1169 | chr7 | 77956047 | |||||
| chr7:77956225
|
T | A | 1 | a0001c0001t0017 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1347T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 1347 | chr7 | 77956225 | |||||
| chr7:77956225
|
T | C | 1 | a0001c0001t0018 | 1 | HG01517.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1347T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 1347 | chr7 | 77956225 | |||||
| chr7:77956232
|
T | C | 1 | a0001c0001t0019 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1354T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 1354 | chr7 | 77956232 | |||||
| chr7:77956390
|
T | C | 1 | a0001c0001t0021 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1512T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 1512 | chr7 | 77956390 | |||||
| chr7:77956416
|
C | T | 1 | a0001c0003t0004 | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1538C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 1538 | chr7 | 77956416 | |||||
| chr7:77956440
|
T | A | 1 | a0001c0002t0022 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1562T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 1562 | chr7 | 77956440 | |||||
| chr7:77956574
|
G | A | 2 | a0001c0001t0010a0001c0001t0017 | 3 | HG02257.hp2 HG02258.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1696G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 1696 | chr7 | 77956574 | |||||
| chr7:77956639
|
G | A | 6 | a0001c0002t0002a0001c0002t0013a0001c0002t0020others(3): Show | 58 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1761G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 1761 | chr7 | 77956639 | |||||
| chr7:77956777
|
G | A | 1 | a0001c0004t0007 | 3 | HG02572.hp1 HG02965.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1899G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 1899 | chr7 | 77956777 | |||||
| chr7:77956927
|
A | T | 1 | a0003c0008t0024 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2049A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 19/19 | 2049 | chr7 | 77956927 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:77799017
|
C | T | 1 | a0001c0001t0001g0314 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-36+46C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77799017 | ||||||
| chr7:77799176
|
T | C | 6 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(3): Show | 6 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36+205T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77799176 | ||||||
| chr7:77799254
|
G | A | 1 | a0001c0001t0001g0007 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-36+283G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77799254 | ||||||
| chr7:77799280
|
C | T | 1 | a0001c0001t0001g0313 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-36+309C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77799280 | ||||||
| chr7:77799452
|
G | A | 4 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36+481G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77799452 | ||||||
| chr7:77799589
|
C | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+618C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77799589 | ||||||
| chr7:77799603
|
A | T | 1 | a0001c0001t0001g0305 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-36+632A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77799603 | ||||||
| chr7:77799823
|
G | A | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+852G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77799823 | ||||||
| chr7:77799954
|
A | G | 1 | a0001c0001t0005g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-36+983A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77799954 | ||||||
| chr7:77800640
|
C | CT | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+1676dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77800640 | |||||
| chr7:77800686
|
A | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-36+1715A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77800686 | ||||||
| chr7:77801118
|
CCTT | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | NA18954.hp1 NA18974.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+2150_-36+2152d others(5): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77801118 | |||||
| chr7:77801163
|
A | G | 1 | a0001c0001t0012g0303 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-36+2192A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77801163 | ||||||
| chr7:77801383
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+2412C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77801383 | ||||||
| chr7:77801455
|
A | G | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-36+2484A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77801455 | ||||||
| chr7:77801778
|
C | T | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+2807C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77801778 | ||||||
| chr7:77802020
|
A | C | 7 | a0001c0001t0001g0295a0001c0001t0001g0297a0001c0001t0001g0298others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+3049A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77802020 | ||||||
| chr7:77802102
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-36+3131G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77802102 | ||||||
| chr7:77802178
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+3207A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77802178 | ||||||
| chr7:77802285
|
G | T | 2 | a0001c0002t0013g0294a0001c0002t0020g0293 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-36+3314G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77802285 | ||||||
| chr7:77802498
|
T | TTTGACTG others(315): Show |
2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-36+3543_-36+3544i others(324): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77802498 | |||||
| chr7:77802588
|
T | C | 1 | a0001c0004t0007g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-36+3617T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77802588 | ||||||
| chr7:77802707
|
T | C | 1 | a0001c0001t0001g0018 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-36+3736T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77802707 | ||||||
| chr7:77802708
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+3737A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77802708 | ||||||
| chr7:77802775
|
C | T | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-36+3804C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77802775 | ||||||
| chr7:77802920
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-36+3949G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77802920 | ||||||
| chr7:77803052
|
C | G | 1 | a0001c0002t0002g0288 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-36+4081C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77803052 | ||||||
| chr7:77803119
|
A | G | 13 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-36+4148A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77803119 | ||||||
| chr7:77803128
|
G | A | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+4157G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77803128 | ||||||
| chr7:77803193
|
A | G | 1 | a0001c0004t0007g0277 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-36+4222A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77803193 | ||||||
| chr7:77803230
|
G | C | 1 | a0001c0001t0023g0278 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-36+4259G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77803230 | ||||||
| chr7:77803258
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-36+4287A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77803258 | ||||||
| chr7:77803574
|
T | C | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+4603T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77803574 | ||||||
| chr7:77803597
|
A | G | 73 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36+4626A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77803597 | ||||||
| chr7:77803627
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-36+4656C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77803627 | ||||||
| chr7:77803686
|
GGCGT | G | 3 | a0001c0002t0002g0215a0001c0002t0002g0216a0001c0002t0002g0217 | 3 | HG01074.hp1 HG01358.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.-36+4717_-36+4720d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77803686 | |||||
| chr7:77803688
|
C | CGT | 18 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(15): Show | 18 | HG00621.hp1 HG00639.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.-36+4754_-36+4755d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77803688 | |||||
| chr7:77803688
|
C | CGTGT | 9 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0267others(6): Show | 9 | HG01255.hp1 HG01255.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36+4752_-36+4755d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77803688 | |||||
| chr7:77803688
|
C | CGTGTGT | 3 | a0001c0001t0001g0274a0001c0001t0005g0304a0001c0006t0001g0275 | 3 | HG01109.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-36+4750_-36+4755d others(8): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77803688 | |||||
| chr7:77803688
|
CGT | C | 49 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0074others(46): Show | 49 | HG00280.hp1 HG00735.hp1 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.-36+4754_-36+4755d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77803688 | |||||
| chr7:77803688
|
CGTGT | C | 60 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(57): Show | 60 | HG00639.hp1 HG00741.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.-36+4752_-36+4755d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77803688 | |||||
| chr7:77803688
|
CGTGTGTG others(5): Show |
C | 3 | a0001c0001t0001g0020a0001c0001t0001g0218a0001c0001t0001g0219 | 3 | HG02896.hp2 HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-36+4744_-36+4755d others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77803688 | |||||
| chr7:77803898
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-36+4927T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77803898 | ||||||
| chr7:77804011
|
TAAGTGTA others(2): Show |
T | 4 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG00639.hp2 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36+5041_-36+5049d others(11): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77804011 | ||||||
| chr7:77804167
|
A | C | 131 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(128): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.-36+5196A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77804167 | ||||||
| chr7:77804287
|
A | G | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-36+5316A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77804287 | ||||||
| chr7:77804323
|
TTTTG | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+5369_-36+5372d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77804323 | |||||
| chr7:77804373
|
G | T | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-36+5402G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77804373 | ||||||
| chr7:77804450
|
C | T | 3 | a0001c0001t0001g0261a0001c0002t0001g0289a0001c0002t0016g0290 | 3 | HG02559.hp2 HG03516.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.-36+5479C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77804450 | ||||||
| chr7:77804463
|
T | G | 2 | a0001c0002t0013g0294a0001c0002t0020g0293 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-36+5492T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77804463 | ||||||
| chr7:77804556
|
C | T | 1 | a0001c0002t0022g0080 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-36+5585C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77804556 | ||||||
| chr7:77804898
|
T | C | 79 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(76): Show | 79 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(76): Show |
intron_variant | MODIFIER | c.-36+5927T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77804898 | ||||||
| chr7:77804921
|
C | G | 4 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071others(1): Show | 4 | HG02257.hp2 HG02258.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36+5950C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77804921 | ||||||
| chr7:77804926
|
A | G | 2 | a0001c0001t0001g0264a0001c0001t0006g0265 | 2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-36+5955A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77804926 | ||||||
| chr7:77805036
|
G | C | 1 | a0001c0001t0001g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-36+6065G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77805036 | ||||||
| chr7:77805768
|
G | A | 83 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(80): Show | 83 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.-36+6797G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77805768 | ||||||
| chr7:77805796
|
G | A | 1 | a0001c0004t0007g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-36+6825G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77805796 | ||||||
| chr7:77805996
|
GA | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+7028delA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77805996 | |||||
| chr7:77806026
|
G | T | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-36+7055G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77806026 | ||||||
| chr7:77806056
|
T | C | 5 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+7085T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77806056 | ||||||
| chr7:77806164
|
C | CA | 84 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(81): Show | 84 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.-36+7207dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77806164 | |||||
| chr7:77806186
|
C | G | 1 | a0001c0001t0001g0200 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-36+7215C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77806186 | ||||||
| chr7:77806357
|
A | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-36+7386A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77806357 | ||||||
| chr7:77806639
|
C | G | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-36+7668C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77806639 | ||||||
| chr7:77807117
|
A | G | 1 | a0001c0001t0001g0301 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-36+8146A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77807117 | ||||||
| chr7:77807168
|
C | T | 152 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(149): Show | 152 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-36+8197C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77807168 | ||||||
| chr7:77807187
|
A | C | 69 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(66): Show | 69 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.-36+8216A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77807187 | ||||||
| chr7:77807372
|
GT | G | 67 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(64): Show | 67 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.-36+8411delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77807372 | |||||
| chr7:77807565
|
G | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-36+8594G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77807565 | ||||||
| chr7:77807608
|
C | T | 1 | a0001c0002t0002g0065 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-36+8637C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77807608 | ||||||
| chr7:77807908
|
T | C | 1 | a0001c0002t0002g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-36+8937T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77807908 | ||||||
| chr7:77808013
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-36+9042G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77808013 | ||||||
| chr7:77808119
|
C | T | 3 | a0001c0002t0002g0062a0001c0002t0002g0063a0001c0002t0002g0064 | 3 | NA18953.hp2 NA18960.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-36+9148C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77808119 | ||||||
| chr7:77808136
|
C | G | 1 | a0001c0002t0002g0061 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-36+9165C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77808136 | ||||||
| chr7:77808400
|
A | G | 4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 4 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36+9429A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77808400 | ||||||
| chr7:77808646
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-36+9675A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77808646 | ||||||
| chr7:77808777
|
C | T | 4 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG00639.hp2 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36+9806C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77808777 | ||||||
| chr7:77808822
|
G | T | 1 | a0001c0002t0025g0060 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-36+9851G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77808822 | ||||||
| chr7:77808859
|
A | G | 1 | a0001c0002t0016g0290 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-36+9888A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77808859 | ||||||
| chr7:77808959
|
A | G | 70 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(67): Show | 70 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.-36+9988A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77808959 | ||||||
| chr7:77809175
|
T | A | 62 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(59): Show | 62 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.-36+10204T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77809175 | ||||||
| chr7:77809177
|
A | G | 62 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(59): Show | 62 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.-36+10206A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77809177 | ||||||
| chr7:77809224
|
G | GT | 6 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 6 | HG01099.hp2 HG03831.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36+10273dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77809224 | |||||
| chr7:77809224
|
G | GTTTTTTT others(1): Show |
12 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0005g0025others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36+10266_-36+1027 others(12): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77809224 | |||||
| chr7:77809224
|
G | GTTTTTTT others(2): Show |
43 | a0001c0001t0001g0030a0001c0001t0001g0302a0001c0001t0003g0306others(40): Show | 43 | HG00639.hp1 HG00733.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.-36+10265_-36+1027 others(13): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77809224 | |||||
| chr7:77809224
|
G | GTTTTTTT others(3): Show |
21 | a0001c0001t0001g0056a0001c0001t0003g0310a0001c0001t0003g0311others(18): Show | 21 | HG00741.hp2 HG01074.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.-36+10264_-36+1027 others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77809224 | |||||
| chr7:77809224
|
G | GTTTTTTT others(6): Show |
3 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004 | 3 | HG00140.hp1 HG00642.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-36+10261_-36+1027 others(17): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77809224 | |||||
| chr7:77809224
|
G | GTTTTTTT others(7): Show |
2 | a0001c0003t0004g0005a0001c0003t0004g0006 | 2 | HG01256.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-36+10260_-36+1027 others(18): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77809224 | |||||
| chr7:77809224
|
GT | G | 128 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(125): Show | 128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-36+10273delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77809224 | |||||
| chr7:77809442
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-36+10471G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77809442 | ||||||
| chr7:77809486
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-36+10515C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77809486 | ||||||
| chr7:77809739
|
C | T | 1 | a0001c0001t0001g0259 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-36+10768C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77809739 | ||||||
| chr7:77809794
|
T | C | 1 | a0001c0002t0002g0215 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-36+10823T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77809794 | ||||||
| chr7:77809845
|
T | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+10874T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77809845 | ||||||
| chr7:77810099
|
G | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-36+11128G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77810099 | ||||||
| chr7:77810406
|
G | C | 2 | a0001c0001t0009g0176a0001c0001t0009g0177 | 2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-36+11435G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77810406 | ||||||
| chr7:77810536
|
C | T | 3 | a0001c0002t0002g0215a0001c0002t0002g0216a0001c0002t0002g0217 | 3 | HG01074.hp1 HG01358.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.-36+11565C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77810536 | ||||||
| chr7:77810594
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-36+11623G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77810594 | ||||||
| chr7:77810599
|
A | G | 76 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(73): Show | 76 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.-36+11628A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77810599 | ||||||
| chr7:77810705
|
T | C | 1 | a0001c0001t0001g0224 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-36+11734T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77810705 | ||||||
| chr7:77810951
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+11980T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77810951 | ||||||
| chr7:77810989
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-36+12018C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77810989 | ||||||
| chr7:77810990
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-36+12019G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77810990 | ||||||
| chr7:77811029
|
A | G | 4 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36+12058A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77811029 | ||||||
| chr7:77811157
|
C | A | 1 | a0001c0001t0001g0074 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-36+12186C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77811157 | ||||||
| chr7:77811240
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG02027.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.-36+12269A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77811240 | ||||||
| chr7:77811586
|
AT | A | 3 | a0001c0001t0001g0302a0001c0002t0001g0289a0001c0002t0016g0290 | 3 | HG02559.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-36+12617delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77811586 | |||||
| chr7:77811738
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+12767A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77811738 | ||||||
| chr7:77811923
|
A | G | 1 | a0001c0001t0023g0278 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-36+12952A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77811923 | ||||||
| chr7:77812029
|
A | G | 1 | a0001c0001t0001g0305 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-36+13058A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77812029 | ||||||
| chr7:77812275
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-36+13304G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77812275 | ||||||
| chr7:77812508
|
G | C | 1 | a0001c0002t0002g0028 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-36+13537G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77812508 | ||||||
| chr7:77812565
|
A | C | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-36+13594A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77812565 | ||||||
| chr7:77812593
|
C | CT | 49 | a0001c0001t0001g0056a0001c0001t0001g0167a0001c0001t0001g0168others(46): Show | 49 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.-36+13636dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77812593 | |||||
| chr7:77812802
|
G | T | 64 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(61): Show | 64 | HG00099.hp1 HG00423.hp1 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.-36+13831G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77812802 | ||||||
| chr7:77812825
|
G | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG02451.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-36+13854G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77812825 | ||||||
| chr7:77812936
|
C | T | 1 | a0001c0002t0002g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-36+13965C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77812936 | ||||||
| chr7:77813789
|
G | A | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+14818G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77813789 | ||||||
| chr7:77813795
|
T | G | 3 | a0001c0001t0001g0302a0001c0002t0001g0289a0001c0002t0016g0290 | 3 | HG02559.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-36+14824T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77813795 | ||||||
| chr7:77813837
|
T | G | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-36+14866T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77813837 | ||||||
| chr7:77814053
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-36+15082G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77814053 | ||||||
| chr7:77814129
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+15158T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77814129 | ||||||
| chr7:77814227
|
A | C | 3 | a0001c0004t0007g0017a0001c0004t0007g0069a0001c0004t0007g0277 | 3 | HG02572.hp1 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-36+15256A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77814227 | ||||||
| chr7:77814401
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+15430A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77814401 | ||||||
| chr7:77814407
|
T | C | 13 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(10): Show | 13 | HG01192.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-36+15436T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77814407 | ||||||
| chr7:77814414
|
A | G | 5 | a0001c0001t0001g0227a0001c0001t0001g0254a0001c0001t0001g0255others(2): Show | 5 | HG00438.hp2 HG02071.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+15443A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77814414 | ||||||
| chr7:77814513
|
A | AT | 7 | a0001c0001t0001g0168a0001c0002t0001g0289a0001c0002t0002g0011others(4): Show | 7 | HG01099.hp1 HG01192.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+15559dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77814513 | |||||
| chr7:77814513
|
AT | A | 13 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0001g0093others(10): Show | 13 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.-36+15559delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77814513 | |||||
| chr7:77814573
|
G | T | 17 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-36+15602G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77814573 | ||||||
| chr7:77814598
|
A | G | 76 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(73): Show | 76 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.-36+15627A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77814598 | ||||||
| chr7:77814660
|
C | T | 303 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.-36+15689C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77814660 | ||||||
| chr7:77814666
|
C | T | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-36+15695C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77814666 | ||||||
| chr7:77814669
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-36+15698G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77814669 | ||||||
| chr7:77814797
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+15826G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77814797 | ||||||
| chr7:77814808
|
C | G | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 3 | HG01123.hp1 HG01169.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-36+15837C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77814808 | ||||||
| chr7:77815001
|
C | T | 2 | a0001c0001t0005g0025a0001c0001t0005g0026 | 2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-36+16030C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77815001 | ||||||
| chr7:77815010
|
G | A | 40 | a0001c0001t0001g0056a0001c0002t0002g0021a0001c0002t0002g0022others(37): Show | 40 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.-36+16039G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77815010 | ||||||
| chr7:77815045
|
C | A | 1 | a0001c0001t0015g0113 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-36+16074C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77815045 | ||||||
| chr7:77815142
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-36+16171A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77815142 | ||||||
| chr7:77815376
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-36+16405G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77815376 | ||||||
| chr7:77815440
|
C | T | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+16469C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77815440 | ||||||
| chr7:77815770
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-36+16799G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77815770 | ||||||
| chr7:77815867
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-36+16896C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77815867 | ||||||
| chr7:77815962
|
G | A | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+16991G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77815962 | ||||||
| chr7:77816185
|
G | A | 1 | a0001c0002t0002g0097 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-36+17214G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77816185 | ||||||
| chr7:77816311
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | NA18960.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-36+17340G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77816311 | ||||||
| chr7:77816648
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+17677A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77816648 | ||||||
| chr7:77816695
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-36+17724C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77816695 | ||||||
| chr7:77816849
|
G | A | 2 | a0001c0002t0002g0049a0001c0002t0002g0050 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-36+17878G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77816849 | ||||||
| chr7:77816887
|
C | T | 1 | a0001c0002t0002g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-36+17916C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77816887 | ||||||
| chr7:77816912
|
A | G | 3 | a0001c0001t0001g0078a0001c0001t0001g0112a0001c0001t0001g0213 | 3 | HG00735.hp2 HG01255.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-36+17941A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77816912 | ||||||
| chr7:77816983
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-36+18012G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77816983 | ||||||
| chr7:77817392
|
T | C | 4 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG00639.hp2 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36+18421T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77817392 | ||||||
| chr7:77817473
|
C | T | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+18502C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77817473 | ||||||
| chr7:77817509
|
C | G | 1 | a0001c0001t0001g0214 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-36+18538C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77817509 | ||||||
| chr7:77817581
|
A | G | 4 | a0001c0001t0001g0018a0001c0001t0001g0196a0001c0001t0001g0197others(1): Show | 4 | HG02071.hp1 NA18612.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36+18610A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77817581 | ||||||
| chr7:77817604
|
TC | T | 65 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(62): Show | 65 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.-36+18636delC | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77817604 | |||||
| chr7:77817610
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG00280.hp1 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-36+18639C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77817610 | ||||||
| chr7:77817826
|
C | T | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-36+18855C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77817826 | ||||||
| chr7:77817876
|
A | G | 83 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(80): Show | 83 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.-36+18905A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77817876 | ||||||
| chr7:77817906
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-36+18935G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77817906 | ||||||
| chr7:77818059
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+19088G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77818059 | ||||||
| chr7:77818110
|
C | CA | 8 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0175others(5): Show | 8 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.-36+19154dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77818110 | |||||
| chr7:77818275
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-36+19304A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77818275 | ||||||
| chr7:77818623
|
T | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+19652T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77818623 | ||||||
| chr7:77818729
|
C | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-36+19758C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77818729 | ||||||
| chr7:77818850
|
T | TAATAATA others(328): Show |
1 | a0001c0001t0001g0209 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-36+19894_-36+1989 others(339): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77818850 | |||||
| chr7:77818850
|
T | TAATAATA others(332): Show |
1 | a0001c0001t0001g0074 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-36+19894_-36+1989 others(343): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77818850 | |||||
| chr7:77818861
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+19890T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77818861 | ||||||
| chr7:77818871
|
T | C | 1 | a0001c0001t0001g0224 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-36+19900T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77818871 | ||||||
| chr7:77818985
|
C | T | 2 | a0001c0001t0005g0085a0001c0001t0005g0304 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-36+20014C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77818985 | ||||||
| chr7:77819052
|
GT | G | 6 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0119others(3): Show | 6 | HG01257.hp2 HG01943.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.-36+20084delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77819052 | |||||
| chr7:77819057
|
G | T | 6 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0119others(3): Show | 6 | HG01257.hp2 HG01943.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.-36+20086G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77819057 | ||||||
| chr7:77819076
|
A | T | 83 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(80): Show | 83 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.-36+20105A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77819076 | ||||||
| chr7:77819199
|
C | T | 1 | a0001c0001t0021g0312 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-36+20228C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77819199 | ||||||
| chr7:77819354
|
T | C | 62 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(59): Show | 62 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.-36+20383T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77819354 | ||||||
| chr7:77819363
|
C | T | 65 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(62): Show | 65 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.-36+20392C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77819363 | ||||||
| chr7:77819389
|
A | G | 1 | a0001c0001t0005g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-36+20418A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77819389 | ||||||
| chr7:77819547
|
A | G | 1 | a0001c0002t0002g0065 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-36+20576A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77819547 | ||||||
| chr7:77819567
|
G | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0193a0001c0001t0001g0194others(5): Show | 8 | HG02027.hp1 HG02071.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.-36+20596G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77819567 | ||||||
| chr7:77819817
|
C | A | 3 | a0001c0004t0007g0017a0001c0004t0007g0069a0001c0004t0007g0277 | 3 | HG02572.hp1 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-35-20404C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77819817 | ||||||
| chr7:77819828
|
G | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-20393G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77819828 | ||||||
| chr7:77820052
|
G | A | 2 | a0001c0001t0005g0085a0001c0001t0005g0304 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-35-20169G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77820052 | ||||||
| chr7:77820179
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-35-20042G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77820179 | ||||||
| chr7:77820188
|
T | G | 4 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG00639.hp2 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35-20033T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77820188 | ||||||
| chr7:77820276
|
G | T | 1 | a0001c0002t0002g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-35-19945G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77820276 | ||||||
| chr7:77820281
|
A | G | 71 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(68): Show | 71 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-35-19940A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77820281 | ||||||
| chr7:77820412
|
C | T | 2 | a0001c0001t0001g0272a0001c0001t0003g0311 | 2 | HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-35-19809C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77820412 | ||||||
| chr7:77820544
|
T | G | 216 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(213): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-35-19677T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77820544 | ||||||
| chr7:77820553
|
C | T | 1 | a0001c0002t0002g0047 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-35-19668C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77820553 | ||||||
| chr7:77820561
|
A | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0198 | 2 | NA18990.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-35-19660A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77820561 | ||||||
| chr7:77820575
|
G | T | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-35-19646G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77820575 | ||||||
| chr7:77820628
|
C | A | 1 | a0001c0001t0001g0313 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-35-19593C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77820628 | ||||||
| chr7:77820798
|
C | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | NA18945.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.-35-19423C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77820798 | ||||||
| chr7:77820871
|
T | C | 1 | a0001c0001t0017g0071 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-35-19350T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77820871 | ||||||
| chr7:77821041
|
T | C | 68 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(65): Show | 68 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.-35-19180T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77821041 | ||||||
| chr7:77821064
|
G | C | 1 | a0001c0002t0002g0288 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-35-19157G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77821064 | ||||||
| chr7:77821126
|
GT | G | 64 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(61): Show | 64 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.-35-19083delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77821126 | |||||
| chr7:77821126
|
GTT | G | 65 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(62): Show | 65 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.-35-19084_-35-1908 others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77821126 | |||||
| chr7:77821126
|
GTTT | G | 82 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(79): Show | 82 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.-35-19085_-35-1908 others(7): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77821126 | |||||
| chr7:77821170
|
C | G | 7 | a0001c0002t0001g0289a0001c0002t0016g0290a0001c0003t0004g0002others(4): Show | 7 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.-35-19051C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77821170 | ||||||
| chr7:77821444
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-35-18777C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77821444 | ||||||
| chr7:77821566
|
G | T | 1 | a0001c0001t0001g0252 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-35-18655G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77821566 | ||||||
| chr7:77821679
|
C | G | 1 | a0001c0001t0018g0160 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-35-18542C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77821679 | ||||||
| chr7:77821949
|
T | C | 1 | a0001c0001t0003g0306 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-35-18272T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77821949 | ||||||
| chr7:77822045
|
C | T | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-35-18176C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77822045 | ||||||
| chr7:77822363
|
A | C | 1 | a0001c0001t0006g0300 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-35-17858A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77822363 | ||||||
| chr7:77822391
|
G | A | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-35-17830G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77822391 | ||||||
| chr7:77822421
|
G | A | 1 | a0001c0001t0006g0300 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-35-17800G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77822421 | ||||||
| chr7:77822486
|
C | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-35-17735C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77822486 | ||||||
| chr7:77822495
|
C | T | 213 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(210): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.-35-17726C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77822495 | ||||||
| chr7:77822787
|
C | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-35-17434C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77822787 | ||||||
| chr7:77822829
|
T | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-35-17392T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77822829 | ||||||
| chr7:77822829
|
T | G | 162 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(159): Show | 162 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-35-17392T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77822829 | ||||||
| chr7:77822904
|
CT | C | 194 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(191): Show | 194 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-35-17299delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77822904 | |||||
| chr7:77822927
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-35-17294C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77822927 | ||||||
| chr7:77823078
|
C | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-35-17143C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77823078 | ||||||
| chr7:77823113
|
C | T | 75 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(72): Show | 75 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-35-17108C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77823113 | ||||||
| chr7:77823196
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-35-17025G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77823196 | ||||||
| chr7:77823244
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-16977C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77823244 | ||||||
| chr7:77823316
|
G | A | 5 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG00099.hp1 HG00741.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.-35-16905G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77823316 | ||||||
| chr7:77823371
|
C | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-35-16850C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77823371 | ||||||
| chr7:77823423
|
G | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-16798G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77823423 | ||||||
| chr7:77823497
|
G | C | 1 | a0001c0001t0005g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-35-16724G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77823497 | ||||||
| chr7:77823711
|
CTGTGTAG others(15): Show |
C | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-35-16492_-35-1647 others(26): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77823711 | |||||
| chr7:77823930
|
A | G | 4 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG00639.hp2 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35-16291A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77823930 | ||||||
| chr7:77824040
|
G | A | 65 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(62): Show | 65 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.-35-16181G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77824040 | ||||||
| chr7:77824227
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-15994A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77824227 | ||||||
| chr7:77824259
|
G | T | 3 | a0001c0001t0001g0214a0001c0001t0001g0302a0001c0001t0005g0304 | 3 | HG01109.hp2 HG02976.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-35-15962G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77824259 | ||||||
| chr7:77824419
|
A | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG00280.hp1 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-35-15802A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77824419 | ||||||
| chr7:77824563
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-35-15658T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77824563 | ||||||
| chr7:77824655
|
C | T | 1 | a0001c0002t0002g0070 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-35-15566C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77824655 | ||||||
| chr7:77824787
|
T | C | 215 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(212): Show | 215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-35-15434T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77824787 | ||||||
| chr7:77824870
|
C | CA | 13 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0001g0125others(10): Show | 13 | HG00438.hp1 HG00621.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.-35-15338dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77824870 | |||||
| chr7:77825092
|
T | TG | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-35-15125dupG | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77825092 | |||||
| chr7:77825135
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-15086G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77825135 | ||||||
| chr7:77825255
|
C | A | 2 | a0001c0004t0007g0017a0001c0004t0007g0069 | 2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-35-14966C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77825255 | ||||||
| chr7:77825290
|
C | T | 1 | a0001c0002t0022g0080 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-35-14931C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77825290 | ||||||
| chr7:77825444
|
A | T | 1 | a0001c0001t0001g0214 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-35-14777A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77825444 | ||||||
| chr7:77825677
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-35-14544G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77825677 | ||||||
| chr7:77825743
|
G | C | 67 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(64): Show | 67 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.-35-14478G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77825743 | ||||||
| chr7:77825812
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-35-14409G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77825812 | ||||||
| chr7:77825951
|
T | C | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-35-14270T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77825951 | ||||||
| chr7:77826034
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0111 | 2 | HG01167.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-35-14187A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77826034 | ||||||
| chr7:77826264
|
A | G | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-35-13957A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77826264 | ||||||
| chr7:77826582
|
A | G | 166 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(163): Show | 166 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.-35-13639A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77826582 | ||||||
| chr7:77826728
|
A | G | 1 | a0001c0002t0002g0288 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-35-13493A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77826728 | ||||||
| chr7:77826983
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-35-13238A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77826983 | ||||||
| chr7:77827423
|
C | T | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-35-12798C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77827423 | ||||||
| chr7:77827433
|
T | C | 83 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(80): Show | 83 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.-35-12788T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77827433 | ||||||
| chr7:77827535
|
G | A | 1 | a0001c0002t0022g0080 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-35-12686G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77827535 | ||||||
| chr7:77827579
|
C | T | 5 | a0001c0001t0001g0227a0001c0001t0001g0254a0001c0001t0001g0255others(2): Show | 5 | HG00438.hp2 HG02071.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-12642C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77827579 | ||||||
| chr7:77827673
|
C | T | 65 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(62): Show | 65 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.-35-12548C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77827673 | ||||||
| chr7:77827927
|
A | C | 1 | a0001c0001t0001g0267 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-35-12294A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77827927 | ||||||
| chr7:77828052
|
A | G | 1 | a0001c0002t0002g0046 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-35-12169A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77828052 | ||||||
| chr7:77828230
|
T | A | 2 | a0001c0002t0013g0294a0001c0002t0020g0293 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-35-11991T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77828230 | ||||||
| chr7:77828261
|
T | C | 1 | a0001c0002t0002g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-35-11960T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77828261 | ||||||
| chr7:77828279
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-35-11942C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77828279 | ||||||
| chr7:77828315
|
G | A | 15 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(12): Show | 15 | HG01192.hp1 HG01243.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-35-11906G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77828315 | ||||||
| chr7:77828520
|
A | G | 1 | a0001c0002t0002g0067 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-35-11701A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77828520 | ||||||
| chr7:77828604
|
A | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG01071.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-35-11617A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77828604 | ||||||
| chr7:77828760
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-35-11461C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77828760 | ||||||
| chr7:77828777
|
A | C | 45 | a0001c0001t0001g0056a0001c0002t0002g0021a0001c0002t0002g0022others(42): Show | 45 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.-35-11444A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77828777 | ||||||
| chr7:77828850
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-35-11371A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77828850 | ||||||
| chr7:77829001
|
C | T | 2 | a0001c0001t0005g0085a0001c0001t0005g0304 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-35-11220C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77829001 | ||||||
| chr7:77829195
|
A | C | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-35-11026A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77829195 | ||||||
| chr7:77829461
|
C | T | 71 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(68): Show | 71 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-35-10760C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77829461 | ||||||
| chr7:77829763
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-35-10458A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77829763 | ||||||
| chr7:77829865
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-35-10356G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77829865 | ||||||
| chr7:77830008
|
C | T | 82 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(79): Show | 82 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.-35-10213C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77830008 | ||||||
| chr7:77830078
|
G | A | 1 | a0001c0001t0003g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-35-10143G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77830078 | ||||||
| chr7:77830134
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-35-10087G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77830134 | ||||||
| chr7:77830584
|
T | G | 1 | a0001c0001t0001g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-35-9637T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77830584 | ||||||
| chr7:77830634
|
A | G | 2 | a0001c0002t0013g0294a0001c0002t0020g0293 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-35-9587A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77830634 | ||||||
| chr7:77830642
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-35-9579G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77830642 | ||||||
| chr7:77830830
|
A | G | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-35-9391A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77830830 | ||||||
| chr7:77830924
|
A | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-9297A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77830924 | ||||||
| chr7:77831103
|
A | G | 44 | a0001c0002t0002g0021a0001c0002t0002g0022a0001c0002t0002g0027others(41): Show | 44 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.-35-9118A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77831103 | ||||||
| chr7:77831178
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-9043C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77831178 | ||||||
| chr7:77831347
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-35-8874C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77831347 | ||||||
| chr7:77831386
|
G | A | 1 | a0001c0002t0002g0061 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-35-8835G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77831386 | ||||||
| chr7:77831631
|
T | G | 1 | a0001c0001t0001g0128 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-35-8590T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77831631 | ||||||
| chr7:77831679
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-35-8542T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77831679 | ||||||
| chr7:77831779
|
C | T | 2 | a0001c0001t0005g0085a0001c0001t0005g0304 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-35-8442C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77831779 | ||||||
| chr7:77831799
|
TC | T | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-35-8420delC | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77831799 | |||||
| chr7:77831801
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-35-8420C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77831801 | ||||||
| chr7:77831878
|
A | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-8343A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77831878 | ||||||
| chr7:77831961
|
T | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-35-8260T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77831961 | ||||||
| chr7:77831970
|
G | A | 2 | a0002c0005t0001g0189a0002c0005t0001g0190 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.-35-8251G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77831970 | ||||||
| chr7:77832033
|
AT | A | 68 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(65): Show | 68 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.-35-8172delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77832033 | |||||
| chr7:77832064
|
C | T | 5 | a0001c0001t0001g0232a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | NA18980.hp1 NA19056.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-8157C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77832064 | ||||||
| chr7:77832088
|
C | A | 2 | a0001c0001t0005g0085a0001c0001t0005g0304 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-35-8133C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77832088 | ||||||
| chr7:77832464
|
A | G | 10 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35-7757A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77832464 | ||||||
| chr7:77832820
|
A | T | 1 | a0001c0001t0001g0159 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-35-7401A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77832820 | ||||||
| chr7:77832998
|
G | GTC | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-7222_-35-7221i others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77832998 | |||||
| chr7:77833018
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-35-7203A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77833018 | ||||||
| chr7:77833140
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-35-7081A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77833140 | ||||||
| chr7:77833163
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-35-7058G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77833163 | ||||||
| chr7:77833181
|
T | C | 67 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(64): Show | 67 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-35-7040T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77833181 | ||||||
| chr7:77833406
|
T | G | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-35-6815T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77833406 | ||||||
| chr7:77833802
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-35-6419G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77833802 | ||||||
| chr7:77833815
|
C | T | 1 | a0001c0001t0005g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-35-6406C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77833815 | ||||||
| chr7:77833946
|
G | A | 2 | a0001c0001t0009g0176a0001c0001t0009g0177 | 2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-35-6275G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77833946 | ||||||
| chr7:77834267
|
C | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-35-5954C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77834267 | ||||||
| chr7:77834294
|
C | T | 1 | a0001c0001t0005g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-35-5927C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77834294 | ||||||
| chr7:77834312
|
C | CA | 58 | a0001c0001t0001g0019a0001c0001t0001g0081a0001c0001t0001g0082others(55): Show | 58 | HG00438.hp1 HG00642.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.-35-5886dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77834312 | |||||
| chr7:77834312
|
C | CAA | 9 | a0001c0001t0001g0180a0001c0001t0001g0191a0001c0001t0001g0192others(6): Show | 9 | HG00280.hp2 HG00323.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.-35-5887_-35-5886d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77834312 | |||||
| chr7:77834312
|
CA | C | 9 | a0001c0001t0001g0077a0001c0001t0001g0099a0001c0001t0001g0111others(6): Show | 9 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.-35-5886delA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77834312 | |||||
| chr7:77834312
|
CAA | C | 22 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(19): Show | 22 | HG01074.hp1 HG01175.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.-35-5887_-35-5886d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77834312 | |||||
| chr7:77834312
|
CAAA | C | 52 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(49): Show | 52 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.-35-5888_-35-5886d others(5): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77834312 | |||||
| chr7:77834320
|
A | AAAAAAAA others(31): Show |
1 | a0001c0001t0001g0014 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-35-5900_-35-5863d others(40): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77834320 | |||||
| chr7:77834344
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-35-5877G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77834344 | ||||||
| chr7:77834526
|
C | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(63): Show | 66 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.-35-5695C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77834526 | ||||||
| chr7:77834536
|
G | A | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-35-5685G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77834536 | ||||||
| chr7:77834584
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0209 | 2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-35-5637G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77834584 | ||||||
| chr7:77834758
|
T | TAGTCATT others(327): Show |
1 | a0001c0001t0001g0196 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-35-5449_-35-5448i others(336): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77834758 | |||||
| chr7:77834840
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0111 | 2 | HG01167.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-35-5381A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77834840 | ||||||
| chr7:77835002
|
G | T | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-35-5219G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77835002 | ||||||
| chr7:77835274
|
C | CA | 67 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(64): Show | 67 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.-35-4933dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77835274 | |||||
| chr7:77835289
|
C | G | 1 | a0001c0001t0001g0305 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-35-4932C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77835289 | ||||||
| chr7:77835441
|
A | G | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | NA18980.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-35-4780A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77835441 | ||||||
| chr7:77835675
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-35-4546A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77835675 | ||||||
| chr7:77835890
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-35-4331C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77835890 | ||||||
| chr7:77835935
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-35-4286C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77835935 | ||||||
| chr7:77836119
|
C | CA | 12 | a0001c0001t0001g0074a0001c0001t0001g0118a0001c0001t0001g0130others(9): Show | 12 | HG00323.hp1 HG00438.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.-35-4083dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77836119 | |||||
| chr7:77836119
|
C | CAAA | 27 | a0001c0001t0001g0018a0001c0001t0001g0081a0001c0001t0001g0082others(24): Show | 27 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-35-4085_-35-4083d others(5): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77836119 | |||||
| chr7:77836119
|
C | CAAAA | 48 | a0001c0001t0001g0056a0001c0001t0001g0093a0001c0001t0003g0311others(45): Show | 48 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.-35-4086_-35-4083d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77836119 | |||||
| chr7:77836119
|
C | CAAAAA | 27 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(24): Show | 27 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.-35-4087_-35-4083d others(7): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77836119 | |||||
| chr7:77836428
|
A | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-35-3793A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77836428 | ||||||
| chr7:77836524
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-35-3697C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77836524 | ||||||
| chr7:77836698
|
C | G | 72 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(69): Show | 72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-35-3523C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77836698 | ||||||
| chr7:77836734
|
T | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-35-3487T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77836734 | ||||||
| chr7:77836886
|
A | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00423.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-35-3335A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77836886 | ||||||
| chr7:77836974
|
C | CA | 8 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-35-3231dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77836974 | |||||
| chr7:77836974
|
CA | C | 86 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0023others(83): Show | 86 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.-35-3231delA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77836974 | |||||
| chr7:77837037
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-35-3184G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77837037 | ||||||
| chr7:77837090
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-3131A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77837090 | ||||||
| chr7:77837319
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-35-2902C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77837319 | ||||||
| chr7:77837891
|
G | A | 215 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(212): Show | 215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-35-2330G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77837891 | ||||||
| chr7:77837973
|
T | A | 6 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(3): Show | 6 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35-2248T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77837973 | ||||||
| chr7:77837987
|
TGGGTAAA others(9): Show |
T | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-35-2218_-35-2203d others(18): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77837987 | |||||
| chr7:77838142
|
A | C | 72 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(69): Show | 72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-35-2079A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77838142 | ||||||
| chr7:77838198
|
T | C | 4 | a0001c0002t0002g0033a0001c0002t0002g0034a0001c0002t0002g0035others(1): Show | 4 | HG02135.hp1 NA18747.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35-2023T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77838198 | ||||||
| chr7:77838575
|
C | G | 10 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0104others(7): Show | 10 | HG01099.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35-1646C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77838575 | ||||||
| chr7:77838581
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-35-1640T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77838581 | ||||||
| chr7:77838607
|
T | C | 1 | a0001c0003t0004g0002 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-35-1614T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77838607 | ||||||
| chr7:77838616
|
A | G | 10 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0104others(7): Show | 10 | HG01099.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35-1605A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77838616 | ||||||
| chr7:77838634
|
G | A | 1 | a0001c0002t0002g0036 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-35-1587G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77838634 | ||||||
| chr7:77839068
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-1153G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77839068 | ||||||
| chr7:77839120
|
C | T | 67 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(64): Show | 67 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.-35-1101C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77839120 | ||||||
| chr7:77839259
|
C | CTT | 11 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0130others(8): Show | 11 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.-35-961_-35-960dup others(2): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77839259 | |||||
| chr7:77839741
|
G | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-480G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77839741 | ||||||
| chr7:77839875
|
G | T | 2 | a0001c0001t0009g0176a0001c0001t0009g0177 | 2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-35-346G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77839875 | ||||||
| chr7:77839888
|
G | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-333G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77839888 | ||||||
| chr7:77839963
|
TA | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-35-250delA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 77839963 | |||||
| chr7:77839976
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-35-245A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77839976 | ||||||
| chr7:77840083
|
A | C | 1 | a0001c0001t0012g0303 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-35-138A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77840083 | ||||||
| chr7:77840109
|
G | C | 1 | a0001c0001t0006g0300 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-35-112G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77840109 | ||||||
| chr7:77840155
|
T | C | 4 | a0001c0001t0001g0105a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 4 | HG00099.hp2 HG01109.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35-66T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77840155 | ||||||
| chr7:77840169
|
C | T | 65 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(62): Show | 65 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.-35-52C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 1/18 | chr7 | 77840169 | ||||||
| chr7:77840332
|
A | G | 4 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG00642.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+32A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77840332 | ||||||
| chr7:77840371
|
A | T | 4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 4 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+71A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77840371 | ||||||
| chr7:77840386
|
T | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+86T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77840386 | ||||||
| chr7:77840640
|
T | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+340T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77840640 | ||||||
| chr7:77840992
|
T | A | 1 | a0001c0001t0001g0088 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.45+692T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77840992 | ||||||
| chr7:77841007
|
C | T | 4 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG00639.hp2 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+707C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77841007 | ||||||
| chr7:77841011
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0014g0150 | 2 | HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.45+711A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77841011 | ||||||
| chr7:77841056
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+756A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77841056 | ||||||
| chr7:77841075
|
C | CT | 7 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0203others(4): Show | 7 | HG01099.hp2 HG01433.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+795dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77841075 | |||||
| chr7:77841075
|
C | CTTTTT | 58 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(55): Show | 58 | HG00639.hp1 HG00733.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.45+791_45+795dupTT others(3): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77841075 | |||||
| chr7:77841075
|
C | CTTTTTT | 14 | a0001c0001t0001g0302a0001c0001t0003g0306a0001c0001t0003g0307others(11): Show | 14 | HG00741.hp2 HG01175.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.45+790_45+795dupTT others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77841075 | |||||
| chr7:77841075
|
C | CTTTTTTT others(1): Show |
52 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(49): Show | 52 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.45+788_45+795dupTT others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77841075 | |||||
| chr7:77841075
|
C | CTTTTTTT others(2): Show |
15 | a0001c0001t0001g0209a0001c0001t0001g0218a0001c0001t0001g0224others(12): Show | 15 | HG01123.hp2 HG01261.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+787_45+795dupTT others(7): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77841075 | |||||
| chr7:77841075
|
C | CTTTTTTT others(3): Show |
7 | a0001c0001t0001g0219a0001c0001t0001g0266a0001c0001t0001g0274others(4): Show | 7 | HG00639.hp2 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+786_45+795dupTT others(8): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77841075 | |||||
| chr7:77841075
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0001g0183a0001c0001t0001g0273a0001c0001t0005g0304 | 3 | HG01109.hp2 HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.45+785_45+795dupTT others(9): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77841075 | |||||
| chr7:77841075
|
C | CTTTTTTT others(5): Show |
8 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0178others(5): Show | 8 | HG01243.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+784_45+795dupTT others(10): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77841075 | |||||
| chr7:77841075
|
C | CTTTTTTT others(6): Show |
26 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(23): Show | 26 | HG00323.hp2 HG00735.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.45+783_45+795dupTT others(11): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77841075 | |||||
| chr7:77841075
|
C | CTTTTTTT others(7): Show |
8 | a0001c0001t0001g0180a0001c0001t0001g0187a0001c0001t0001g0191others(5): Show | 8 | HG00642.hp2 HG02071.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+782_45+795dupTT others(12): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77841075 | |||||
| chr7:77841075
|
C | CTTTTTTT others(8): Show |
12 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0195others(9): Show | 12 | HG00280.hp1 HG00280.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.45+781_45+795dupTT others(13): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77841075 | |||||
| chr7:77841075
|
C | CTTTTTTT others(9): Show |
4 | a0001c0001t0001g0091a0001c0001t0001g0284a0001c0001t0001g0286others(1): Show | 4 | HG02145.hp1 HG03209.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+780_45+795dupTT others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77841075 | |||||
| chr7:77841075
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.45+786_45+795delTT others(8): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77841075 | |||||
| chr7:77841129
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.45+829G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77841129 | ||||||
| chr7:77841140
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+840C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77841140 | ||||||
| chr7:77841149
|
G | A | 3 | a0001c0002t0013g0294a0001c0002t0020g0293a0003c0008t0024g0001 | 3 | HG01099.hp1 HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.45+849G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77841149 | ||||||
| chr7:77841545
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+1245A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77841545 | ||||||
| chr7:77841564
|
A | G | 29 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(26): Show | 29 | HG00423.hp1 HG01943.hp1 HG01952.hp1 others(26): Show |
intron_variant | MODIFIER | c.45+1264A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77841564 | ||||||
| chr7:77841577
|
A | G | 1 | a0001c0002t0002g0035 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.45+1277A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77841577 | ||||||
| chr7:77841892
|
C | A | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.45+1592C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77841892 | ||||||
| chr7:77841907
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+1607C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77841907 | ||||||
| chr7:77842063
|
C | T | 2 | a0001c0002t0013g0294a0001c0002t0020g0293 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.45+1763C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77842063 | ||||||
| chr7:77842080
|
C | A | 1 | a0001c0002t0002g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.45+1780C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77842080 | ||||||
| chr7:77842299
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.45+1999G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77842299 | ||||||
| chr7:77842593
|
C | G | 8 | a0001c0001t0001g0175a0001c0001t0001g0180a0001c0001t0001g0182others(5): Show | 8 | HG01192.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+2293C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77842593 | ||||||
| chr7:77842696
|
C | G | 2 | a0001c0002t0013g0294a0001c0002t0020g0293 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.45+2396C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77842696 | ||||||
| chr7:77842744
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+2444T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77842744 | ||||||
| chr7:77842746
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.45+2446T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77842746 | ||||||
| chr7:77842886
|
T | C | 68 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(65): Show | 68 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.45+2586T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77842886 | ||||||
| chr7:77843506
|
C | CCTGA | 68 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(65): Show | 68 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.45+3207_45+3210dup others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77843506 | |||||
| chr7:77843579
|
T | A | 8 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG00621.hp1 NA18747.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+3279T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77843579 | ||||||
| chr7:77843594
|
G | C | 4 | a0001c0002t0001g0289a0001c0002t0013g0294a0001c0002t0016g0290others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+3294G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77843594 | ||||||
| chr7:77843712
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+3412T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77843712 | ||||||
| chr7:77843814
|
T | A | 1 | a0001c0001t0001g0135 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.45+3514T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77843814 | ||||||
| chr7:77844088
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.45+3788C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77844088 | ||||||
| chr7:77844182
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.45+3882C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77844182 | ||||||
| chr7:77844203
|
A | G | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.45+3903A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77844203 | ||||||
| chr7:77844254
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+3954G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77844254 | ||||||
| chr7:77844474
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.45+4174T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77844474 | ||||||
| chr7:77844655
|
G | C | 4 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+4355G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77844655 | ||||||
| chr7:77844724
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+4424T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77844724 | ||||||
| chr7:77844775
|
G | A | 1 | a0001c0001t0019g0066 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.45+4475G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77844775 | ||||||
| chr7:77844819
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+4519C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77844819 | ||||||
| chr7:77844820
|
C | T | 2 | a0001c0001t0005g0085a0001c0001t0005g0304 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.45+4520C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77844820 | ||||||
| chr7:77845220
|
T | C | 82 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(79): Show | 82 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.45+4920T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77845220 | ||||||
| chr7:77845228
|
T | C | 1 | a0001c0001t0001g0016 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.45+4928T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77845228 | ||||||
| chr7:77845229
|
C | T | 1 | a0001c0001t0018g0160 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.45+4929C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77845229 | ||||||
| chr7:77845373
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+5073C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77845373 | ||||||
| chr7:77845414
|
A | T | 4 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+5114A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77845414 | ||||||
| chr7:77845644
|
C | G | 82 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(79): Show | 82 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.45+5344C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77845644 | ||||||
| chr7:77845692
|
G | C | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+5392G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77845692 | ||||||
| chr7:77845716
|
A | G | 3 | a0001c0004t0007g0017a0001c0004t0007g0069a0001c0004t0007g0277 | 3 | HG02572.hp1 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.45+5416A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77845716 | ||||||
| chr7:77845719
|
A | G | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.45+5419A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77845719 | ||||||
| chr7:77845879
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.45+5579G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77845879 | ||||||
| chr7:77845954
|
C | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | NA18983.hp1 NA19009.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.45+5654C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77845954 | ||||||
| chr7:77846105
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.45+5805G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77846105 | ||||||
| chr7:77846142
|
C | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG02451.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.45+5842C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77846142 | ||||||
| chr7:77846223
|
C | T | 1 | a0001c0001t0005g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.45+5923C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77846223 | ||||||
| chr7:77846378
|
C | G | 1 | a0001c0001t0019g0066 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.45+6078C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77846378 | ||||||
| chr7:77846534
|
TTTCCCTT others(3): Show |
T | 1 | a0001c0001t0005g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.45+6241_45+6250del others(10): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77846534 | |||||
| chr7:77846557
|
CCCTCCCC others(3): Show |
C | 216 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(213): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.45+6294_45+6303del others(10): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77846557 | |||||
| chr7:77846567
|
G | C | 1 | a0001c0001t0005g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.45+6267G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77846567 | ||||||
| chr7:77846577
|
G | A | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.45+6277G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77846577 | ||||||
| chr7:77846594
|
C | T | 1 | a0001c0002t0002g0028 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.45+6294C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77846594 | ||||||
| chr7:77846597
|
G | C | 1 | a0001c0002t0002g0028 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.45+6297G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77846597 | ||||||
| chr7:77846611
|
C | T | 1 | a0001c0002t0002g0028 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.45+6311C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77846611 | ||||||
| chr7:77846614
|
T | C | 1 | a0001c0002t0002g0028 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.45+6314T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77846614 | ||||||
| chr7:77846621
|
T | C | 1 | a0001c0002t0002g0028 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.45+6321T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77846621 | ||||||
| chr7:77846706
|
A | T | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+6406A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77846706 | ||||||
| chr7:77846935
|
G | A | 62 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(59): Show | 62 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.45+6635G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77846935 | ||||||
| chr7:77846949
|
T | C | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.45+6649T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77846949 | ||||||
| chr7:77846991
|
G | T | 62 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(59): Show | 62 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.45+6691G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77846991 | ||||||
| chr7:77847056
|
A | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+6756A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77847056 | ||||||
| chr7:77847271
|
A | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+6971A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77847271 | ||||||
| chr7:77847295
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | NA18960.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.45+6995A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77847295 | ||||||
| chr7:77847303
|
T | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+7003T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77847303 | ||||||
| chr7:77847312
|
T | G | 5 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(2): Show | 5 | HG02717.hp2 HG02818.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+7012T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77847312 | ||||||
| chr7:77847349
|
A | G | 17 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.45+7049A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77847349 | ||||||
| chr7:77847366
|
TATG | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+7069_45+7071del others(3): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77847366 | |||||
| chr7:77847685
|
A | G | 216 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(213): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.45+7385A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77847685 | ||||||
| chr7:77848077
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.45+7777A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77848077 | ||||||
| chr7:77848219
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.45+7919T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77848219 | ||||||
| chr7:77848281
|
C | T | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+7981C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77848281 | ||||||
| chr7:77848295
|
T | C | 1 | a0001c0001t0005g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.45+7995T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77848295 | ||||||
| chr7:77848410
|
G | A | 4 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | NA18960.hp2 NA19007.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+8110G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77848410 | ||||||
| chr7:77848449
|
C | T | 1 | a0001c0002t0002g0070 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+8149C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77848449 | ||||||
| chr7:77848595
|
A | G | 4 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG00642.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+8295A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77848595 | ||||||
| chr7:77848711
|
G | A | 5 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0237others(2): Show | 5 | HG01943.hp1 HG01952.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+8411G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77848711 | ||||||
| chr7:77848752
|
T | C | 1 | a0001c0001t0001g0305 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.45+8452T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77848752 | ||||||
| chr7:77848817
|
T | C | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.45+8517T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77848817 | ||||||
| chr7:77849073
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+8773A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77849073 | ||||||
| chr7:77849099
|
T | C | 2 | a0002c0005t0001g0189a0002c0005t0001g0190 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.45+8799T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77849099 | ||||||
| chr7:77849308
|
T | A | 1 | a0001c0001t0001g0252 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.45+9008T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77849308 | ||||||
| chr7:77849330
|
A | G | 1 | a0001c0001t0009g0177 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.45+9030A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77849330 | ||||||
| chr7:77849471
|
A | G | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.45+9171A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77849471 | ||||||
| chr7:77849677
|
T | A | 50 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.45+9377T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77849677 | ||||||
| chr7:77849749
|
A | C | 1 | a0001c0001t0001g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.45+9449A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77849749 | ||||||
| chr7:77850001
|
T | TTC | 216 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(213): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.45+9703_45+9704dup others(2): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850001 | |||||
| chr7:77850037
|
C | T | 67 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(64): Show | 67 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.45+9737C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77850037 | ||||||
| chr7:77850194
|
T | A | 1 | a0001c0001t0001g0123 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.45+9894T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77850194 | ||||||
| chr7:77850194
|
T | TA | 59 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(56): Show | 59 | HG00280.hp1 HG00280.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.45+9912dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850194 | |||||
| chr7:77850194
|
TA | T | 7 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0105others(4): Show | 7 | HG00323.hp1 HG01070.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+9912delA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850194 | |||||
| chr7:77850199
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+9899A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77850199 | ||||||
| chr7:77850360
|
C | CA | 11 | a0001c0001t0001g0125a0001c0001t0001g0135a0001c0001t0001g0137others(8): Show | 11 | HG00423.hp2 HG01175.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+10085dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850360 | |||||
| chr7:77850360
|
C | CAAAAA | 46 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(43): Show | 46 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.45+10081_45+10085d others(7): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850360 | |||||
| chr7:77850360
|
C | CAAAAAA | 21 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0074others(18): Show | 21 | HG00438.hp2 HG01255.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.45+10080_45+10085d others(8): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850360 | |||||
| chr7:77850360
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0003g0306a0001c0001t0003g0309a0001c0001t0003g0311 | 3 | HG02976.hp1 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.45+10076_45+10085d others(12): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850360 | |||||
| chr7:77850360
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0003g0307a0001c0001t0003g0308 | 2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.45+10075_45+10085d others(13): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850360 | |||||
| chr7:77850360
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0021g0312 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.45+10074_45+10085d others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850360 | |||||
| chr7:77850360
|
C | CAAAAAAA others(6): Show |
5 | a0001c0001t0003g0310a0001c0001t0005g0304a0001c0002t0020g0293others(2): Show | 5 | HG01109.hp2 HG02055.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+10073_45+10085d others(15): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850360 | |||||
| chr7:77850360
|
C | CAAAAAAA others(7): Show |
2 | a0001c0003t0004g0004a0001c0003t0004g0006 | 2 | HG00140.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.45+10072_45+10085d others(16): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850360 | |||||
| chr7:77850360
|
C | CAAAAAAA others(9): Show |
1 | a0001c0003t0004g0003 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.45+10070_45+10085d others(18): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850360 | |||||
| chr7:77850360
|
CA | C | 19 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0092others(16): Show | 19 | HG00140.hp2 HG00323.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.45+10085delA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850360 | |||||
| chr7:77850360
|
CAA | C | 26 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(23): Show | 26 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.45+10084_45+10085d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850360 | |||||
| chr7:77850360
|
CAAA | C | 17 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(14): Show | 17 | HG00280.hp2 HG00323.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.45+10083_45+10085d others(5): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850360 | |||||
| chr7:77850360
|
CAAAA | C | 7 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071others(4): Show | 7 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+10082_45+10085d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850360 | |||||
| chr7:77850360
|
CAAAAA | C | 53 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(50): Show | 53 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.45+10081_45+10085d others(7): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850360 | |||||
| chr7:77850641
|
C | CA | 23 | a0001c0001t0001g0056a0001c0001t0001g0074a0001c0001t0001g0089others(20): Show | 23 | HG01109.hp2 HG01256.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.45+10360dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77850641 | |||||
| chr7:77850702
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0135a0001c0001t0001g0174 | 3 | HG02293.hp2 NA18943.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.45+10402G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77850702 | ||||||
| chr7:77850704
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+10404G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77850704 | ||||||
| chr7:77850706
|
A | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+10406A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77850706 | ||||||
| chr7:77851244
|
C | A | 65 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(62): Show | 65 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.45+10944C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77851244 | ||||||
| chr7:77851254
|
G | A | 215 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(212): Show | 215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.45+10954G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77851254 | ||||||
| chr7:77851461
|
T | G | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+11161T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77851461 | ||||||
| chr7:77851599
|
A | AT | 11 | a0001c0001t0001g0126a0001c0001t0001g0280a0001c0001t0001g0281others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.45+11316dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77851599 | |||||
| chr7:77851599
|
AT | A | 7 | a0001c0001t0001g0019a0001c0002t0013g0294a0001c0003t0004g0002others(4): Show | 7 | HG00140.hp1 HG00642.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+11316delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77851599 | |||||
| chr7:77851718
|
C | A | 1 | a0001c0001t0001g0161 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.45+11418C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77851718 | ||||||
| chr7:77851786
|
G | A | 2 | a0001c0001t0005g0085a0001c0001t0005g0304 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.45+11486G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77851786 | ||||||
| chr7:77851870
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.45+11570T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77851870 | ||||||
| chr7:77851961
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0209 | 2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.45+11661C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77851961 | ||||||
| chr7:77851971
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.45+11671C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77851971 | ||||||
| chr7:77852032
|
T | C | 3 | a0001c0002t0002g0031a0001c0002t0002g0048a0001c0002t0002g0058 | 3 | HG02970.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45+11732T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77852032 | ||||||
| chr7:77852034
|
G | T | 19 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0089others(16): Show | 19 | HG00735.hp1 HG01109.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.45+11734G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77852034 | ||||||
| chr7:77852042
|
G | A | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.45+11742G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77852042 | ||||||
| chr7:77852266
|
C | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01433.hp1 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+11966C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77852266 | ||||||
| chr7:77852463
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.45+12163C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77852463 | ||||||
| chr7:77852673
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+12373A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77852673 | ||||||
| chr7:77852683
|
T | A | 20 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(17): Show | 20 | HG00280.hp2 HG00323.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.45+12383T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77852683 | ||||||
| chr7:77852704
|
T | G | 2 | a0001c0002t0013g0294a0001c0002t0020g0293 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.45+12404T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77852704 | ||||||
| chr7:77852805
|
A | G | 50 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.45+12505A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77852805 | ||||||
| chr7:77852834
|
G | T | 1 | a0001c0001t0005g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.45+12534G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77852834 | ||||||
| chr7:77852904
|
A | G | 1 | a0001c0002t0002g0098 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.45+12604A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77852904 | ||||||
| chr7:77852991
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+12691C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77852991 | ||||||
| chr7:77853070
|
C | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+12770C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77853070 | ||||||
| chr7:77853158
|
C | G | 62 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(59): Show | 62 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.45+12858C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77853158 | ||||||
| chr7:77853239
|
T | C | 50 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.45+12939T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77853239 | ||||||
| chr7:77853348
|
C | CA | 69 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(66): Show | 69 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.45+13049dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77853348 | |||||
| chr7:77853395
|
G | T | 1 | a0001c0001t0001g0007 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.45+13095G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77853395 | ||||||
| chr7:77853398
|
AT | A | 72 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(69): Show | 72 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.45+13111delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77853398 | |||||
| chr7:77853405
|
T | C | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.45+13105T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77853405 | ||||||
| chr7:77853453
|
G | C | 20 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(17): Show | 20 | HG00280.hp2 HG00323.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.45+13153G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77853453 | ||||||
| chr7:77853564
|
T | G | 1 | a0001c0001t0001g0135 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.45+13264T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77853564 | ||||||
| chr7:77853583
|
A | G | 1 | a0001c0001t0023g0278 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.45+13283A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77853583 | ||||||
| chr7:77853714
|
T | C | 16 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(13): Show | 16 | HG00423.hp1 HG01943.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+13414T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77853714 | ||||||
| chr7:77854014
|
T | C | 13 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(10): Show | 13 | HG01192.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+13714T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77854014 | ||||||
| chr7:77854114
|
T | C | 2 | a0001c0001t0005g0085a0001c0001t0005g0304 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.45+13814T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77854114 | ||||||
| chr7:77854261
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+13961A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77854261 | ||||||
| chr7:77854302
|
T | G | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+14002T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77854302 | ||||||
| chr7:77854353
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.45+14053T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77854353 | ||||||
| chr7:77854423
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+14123C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77854423 | ||||||
| chr7:77854437
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.45+14137C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77854437 | ||||||
| chr7:77854458
|
G | C | 80 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(77): Show | 80 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.45+14158G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77854458 | ||||||
| chr7:77854499
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.45+14199T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77854499 | ||||||
| chr7:77854560
|
C | A | 1 | a0001c0001t0001g0251 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.45+14260C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77854560 | ||||||
| chr7:77854608
|
G | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.45+14308G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77854608 | ||||||
| chr7:77854646
|
T | G | 4 | a0001c0001t0001g0203a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 4 | HG01099.hp2 HG01433.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+14346T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77854646 | ||||||
| chr7:77854708
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+14408T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77854708 | ||||||
| chr7:77854885
|
T | A | 4 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG00642.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+14585T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77854885 | ||||||
| chr7:77855062
|
G | T | 20 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(17): Show | 20 | HG00280.hp2 HG00323.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.45+14762G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77855062 | ||||||
| chr7:77855145
|
T | C | 1 | a0001c0002t0002g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.45+14845T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77855145 | ||||||
| chr7:77855203
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+14903C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77855203 | ||||||
| chr7:77855294
|
A | G | 12 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.45+14994A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77855294 | ||||||
| chr7:77855624
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+15324G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77855624 | ||||||
| chr7:77855816
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.45+15516G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77855816 | ||||||
| chr7:77856052
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.45+15752A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77856052 | ||||||
| chr7:77856352
|
CTTAT | C | 12 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.45+16067_45+16070d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77856352 | |||||
| chr7:77856415
|
G | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | HG00735.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.45+16115G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77856415 | ||||||
| chr7:77856423
|
A | G | 71 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(68): Show | 71 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.45+16123A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77856423 | ||||||
| chr7:77856502
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.45+16202C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77856502 | ||||||
| chr7:77856590
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+16290G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77856590 | ||||||
| chr7:77856605
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.45+16305C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77856605 | ||||||
| chr7:77856667
|
C | T | 10 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+16367C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77856667 | ||||||
| chr7:77856681
|
A | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+16381A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77856681 | ||||||
| chr7:77856917
|
T | G | 216 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(213): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.45+16617T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77856917 | ||||||
| chr7:77856959
|
G | A | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.45+16659G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77856959 | ||||||
| chr7:77857106
|
C | A | 1 | a0001c0001t0001g0007 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.45+16806C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77857106 | ||||||
| chr7:77857135
|
G | A | 51 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(48): Show | 51 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.45+16835G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77857135 | ||||||
| chr7:77857291
|
A | G | 1 | a0001c0002t0002g0070 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45+16991A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77857291 | ||||||
| chr7:77857359
|
T | C | 83 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(80): Show | 83 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.45+17059T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77857359 | ||||||
| chr7:77857420
|
C | A | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0198 | 3 | HG02135.hp2 NA18990.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.45+17120C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77857420 | ||||||
| chr7:77857623
|
T | C | 1 | a0001c0001t0001g0297 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.45+17323T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77857623 | ||||||
| chr7:77857635
|
C | T | 1 | a0001c0002t0025g0060 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.45+17335C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77857635 | ||||||
| chr7:77857645
|
A | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01433.hp1 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+17345A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77857645 | ||||||
| chr7:77857658
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.45+17358C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77857658 | ||||||
| chr7:77857808
|
A | G | 2 | a0001c0001t0005g0085a0001c0001t0005g0304 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.45+17508A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77857808 | ||||||
| chr7:77858236
|
T | G | 1 | a0001c0001t0001g0007 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.45+17936T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77858236 | ||||||
| chr7:77858592
|
G | T | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.45+18292G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77858592 | ||||||
| chr7:77858649
|
CT | C | 13 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0074others(10): Show | 13 | HG01070.hp1 HG01074.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.45+18365delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77858649 | |||||
| chr7:77858784
|
A | G | 1 | a0001c0003t0004g0004 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.45+18484A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77858784 | ||||||
| chr7:77858880
|
T | A | 1 | a0001c0001t0001g0007 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.45+18580T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77858880 | ||||||
| chr7:77858891
|
C | A | 1 | a0001c0001t0001g0264 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.45+18591C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77858891 | ||||||
| chr7:77858895
|
A | G | 1 | a0001c0001t0001g0313 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.45+18595A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77858895 | ||||||
| chr7:77858999
|
C | G | 65 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(62): Show | 65 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.45+18699C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77858999 | ||||||
| chr7:77859096
|
A | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+18796A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77859096 | ||||||
| chr7:77859117
|
A | T | 65 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(62): Show | 65 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.45+18817A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77859117 | ||||||
| chr7:77859347
|
G | A | 4 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG00423.hp2 NA19054.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+19047G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77859347 | ||||||
| chr7:77859361
|
A | G | 79 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(76): Show | 79 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.45+19061A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77859361 | ||||||
| chr7:77859389
|
C | T | 1 | a0001c0002t0002g0288 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.45+19089C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77859389 | ||||||
| chr7:77859494
|
A | T | 4 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG00639.hp2 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+19194A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77859494 | ||||||
| chr7:77859502
|
T | A | 14 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(11): Show | 14 | HG00140.hp1 HG00642.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.45+19202T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77859502 | ||||||
| chr7:77859564
|
CT | C | 172 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(169): Show | 172 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.45+19281delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77859564 | |||||
| chr7:77859651
|
C | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG02451.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.45+19351C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77859651 | ||||||
| chr7:77859703
|
A | G | 1 | a0001c0001t0005g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.45+19403A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77859703 | ||||||
| chr7:77859909
|
G | A | 3 | a0001c0004t0007g0017a0001c0004t0007g0069a0001c0004t0007g0277 | 3 | HG02572.hp1 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.45+19609G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77859909 | ||||||
| chr7:77859961
|
A | G | 28 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(25): Show | 28 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.45+19661A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77859961 | ||||||
| chr7:77859979
|
A | G | 2 | a0001c0002t0013g0294a0001c0002t0020g0293 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.45+19679A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77859979 | ||||||
| chr7:77859991
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.45+19691G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77859991 | ||||||
| chr7:77860048
|
C | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01433.hp1 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+19748C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77860048 | ||||||
| chr7:77860466
|
T | C | 80 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(77): Show | 80 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.45+20166T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77860466 | ||||||
| chr7:77860524
|
T | A | 1 | a0001c0001t0001g0143 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.45+20224T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77860524 | ||||||
| chr7:77860634
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.45+20334C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77860634 | ||||||
| chr7:77860717
|
G | T | 1 | a0001c0001t0001g0019 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.45+20417G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77860717 | ||||||
| chr7:77860718
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.45+20418C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77860718 | ||||||
| chr7:77860724
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.45+20424T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77860724 | ||||||
| chr7:77860808
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01169.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.45+20508C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77860808 | ||||||
| chr7:77860811
|
A | G | 1 | a0002c0005t0001g0190 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.45+20511A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77860811 | ||||||
| chr7:77860939
|
C | T | 66 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(63): Show | 66 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.45+20639C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77860939 | ||||||
| chr7:77861179
|
A | C | 3 | a0001c0004t0007g0017a0001c0004t0007g0069a0001c0004t0007g0277 | 3 | HG02572.hp1 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.45+20879A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77861179 | ||||||
| chr7:77861415
|
T | A | 1 | a0001c0002t0022g0080 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.45+21115T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77861415 | ||||||
| chr7:77861512
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.45+21212T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77861512 | ||||||
| chr7:77861535
|
A | G | 2 | a0001c0002t0013g0294a0001c0002t0020g0293 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.45+21235A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77861535 | ||||||
| chr7:77861591
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.45+21291G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77861591 | ||||||
| chr7:77861618
|
G | C | 1 | a0001c0002t0002g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.45+21318G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77861618 | ||||||
| chr7:77861701
|
T | A | 69 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(66): Show | 69 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.45+21401T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77861701 | ||||||
| chr7:77861917
|
T | C | 216 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(213): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.45+21617T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77861917 | ||||||
| chr7:77861980
|
C | T | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.45+21680C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77861980 | ||||||
| chr7:77862044
|
C | T | 1 | a0001c0002t0002g0047 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.45+21744C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77862044 | ||||||
| chr7:77862071
|
AG | A | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+21772delG | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77862071 | ||||||
| chr7:77862072
|
G | A | 209 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(206): Show | 209 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.45+21772G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77862072 | ||||||
| chr7:77862107
|
C | T | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.45+21807C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77862107 | ||||||
| chr7:77862160
|
G | T | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+21860G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77862160 | ||||||
| chr7:77862368
|
A | G | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.45+22068A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77862368 | ||||||
| chr7:77862646
|
A | G | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.45+22346A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77862646 | ||||||
| chr7:77862717
|
A | T | 1 | a0001c0001t0001g0199 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.45+22417A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77862717 | ||||||
| chr7:77862748
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+22448A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77862748 | ||||||
| chr7:77862993
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG00280.hp1 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.45+22693G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77862993 | ||||||
| chr7:77863304
|
A | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG00280.hp1 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.45+23004A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77863304 | ||||||
| chr7:77863393
|
G | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+23093G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77863393 | ||||||
| chr7:77863456
|
T | G | 6 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+23156T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77863456 | ||||||
| chr7:77863655
|
C | CT | 9 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0130others(6): Show | 9 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+23367dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77863655 | |||||
| chr7:77863702
|
T | C | 71 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(68): Show | 71 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.45+23402T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77863702 | ||||||
| chr7:77863716
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.45+23416C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77863716 | ||||||
| chr7:77863787
|
G | GT | 122 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(119): Show | 122 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.45+23502dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77863787 | |||||
| chr7:77863787
|
G | GTT | 17 | a0001c0001t0001g0096a0001c0001t0001g0199a0001c0001t0001g0231others(14): Show | 17 | HG00099.hp1 HG00735.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.45+23501_45+23502d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77863787 | |||||
| chr7:77863787
|
GT | G | 77 | a0001c0001t0001g0302a0001c0001t0003g0306a0001c0001t0003g0307others(74): Show | 77 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.45+23502delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77863787 | |||||
| chr7:77863794
|
T | G | 1 | a0001c0001t0001g0125 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.45+23494T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77863794 | ||||||
| chr7:77863849
|
C | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01433.hp1 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+23549C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77863849 | ||||||
| chr7:77864041
|
G | A | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0198others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+23741G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77864041 | ||||||
| chr7:77864138
|
G | A | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+23838G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77864138 | ||||||
| chr7:77864282
|
G | A | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+23982G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77864282 | ||||||
| chr7:77864329
|
A | AT | 4 | a0001c0002t0001g0289a0001c0002t0002g0049a0001c0002t0002g0050others(1): Show | 4 | HG02559.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+24035dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77864329 | |||||
| chr7:77864385
|
C | G | 1 | a0001c0001t0001g0297 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.45+24085C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77864385 | ||||||
| chr7:77864617
|
AT | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG01070.hp2 HG01517.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+24331delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77864617 | |||||
| chr7:77864678
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.45+24378G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77864678 | ||||||
| chr7:77864684
|
C | G | 1 | a0001c0001t0001g0246 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.45+24384C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77864684 | ||||||
| chr7:77864864
|
G | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+24564G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77864864 | ||||||
| chr7:77864926
|
A | T | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.45+24626A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77864926 | ||||||
| chr7:77865031
|
A | G | 45 | a0001c0001t0001g0056a0001c0002t0002g0021a0001c0002t0002g0022others(42): Show | 45 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.45+24731A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77865031 | ||||||
| chr7:77865375
|
G | A | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.45+25075G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77865375 | ||||||
| chr7:77865670
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.45+25370A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77865670 | ||||||
| chr7:77865760
|
C | T | 77 | a0001c0001t0001g0302a0001c0001t0003g0306a0001c0001t0003g0307others(74): Show | 77 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.45+25460C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77865760 | ||||||
| chr7:77865786
|
A | G | 1 | a0001c0002t0002g0046 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.45+25486A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77865786 | ||||||
| chr7:77865849
|
G | A | 1 | a0001c0001t0005g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.45+25549G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77865849 | ||||||
| chr7:77865912
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.45+25612G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77865912 | ||||||
| chr7:77865977
|
A | G | 30 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(27): Show | 30 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.45+25677A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77865977 | ||||||
| chr7:77866184
|
C | CA | 118 | a0001c0001t0001g0019a0001c0001t0001g0056a0001c0001t0001g0081others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.45+25904dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77866184 | |||||
| chr7:77866184
|
C | CAA | 10 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(7): Show | 10 | HG01123.hp1 HG01169.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+25903_45+25904d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77866184 | |||||
| chr7:77866567
|
T | C | 1 | a0001c0002t0002g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.45+26267T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77866567 | ||||||
| chr7:77866642
|
A | T | 1 | a0001c0001t0023g0278 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.45+26342A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77866642 | ||||||
| chr7:77866776
|
T | C | 10 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+26476T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77866776 | ||||||
| chr7:77867068
|
A | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-26540A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77867068 | ||||||
| chr7:77867238
|
A | G | 79 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(76): Show | 79 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.46-26370A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77867238 | ||||||
| chr7:77867566
|
A | G | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.46-26042A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77867566 | ||||||
| chr7:77867714
|
T | C | 1 | a0001c0002t0002g0033 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.46-25894T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77867714 | ||||||
| chr7:77867726
|
T | C | 1 | a0001c0001t0008g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.46-25882T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77867726 | ||||||
| chr7:77867747
|
G | A | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.46-25861G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77867747 | ||||||
| chr7:77867808
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-25800G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77867808 | ||||||
| chr7:77868030
|
A | C | 1 | a0001c0001t0001g0186 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.46-25578A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77868030 | ||||||
| chr7:77868155
|
T | C | 213 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(210): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.46-25453T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77868155 | ||||||
| chr7:77868322
|
A | AT | 34 | a0001c0001t0001g0016a0001c0001t0001g0075a0001c0001t0001g0078others(31): Show | 34 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.46-25258dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77868322 | |||||
| chr7:77868322
|
A | ATT | 8 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0136others(5): Show | 8 | HG00438.hp1 HG01192.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-25259_46-25258d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77868322 | |||||
| chr7:77868322
|
A | T | 1 | a0001c0001t0001g0204 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.46-25286A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77868322 | ||||||
| chr7:77868322
|
AT | A | 42 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(39): Show | 42 | HG00140.hp1 HG00639.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.46-25258delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77868322 | |||||
| chr7:77868322
|
ATT | A | 104 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(101): Show | 104 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.46-25259_46-25258d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77868322 | |||||
| chr7:77868323
|
T | A | 3 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG01071.hp1 HG01074.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.46-25285T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77868323 | ||||||
| chr7:77868397
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.46-25211G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77868397 | ||||||
| chr7:77868403
|
A | G | 215 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(212): Show | 215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.46-25205A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77868403 | ||||||
| chr7:77868452
|
T | A | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-25156T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77868452 | ||||||
| chr7:77868629
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030 | 3 | HG01433.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.46-24979C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77868629 | ||||||
| chr7:77868630
|
G | A | 3 | a0001c0001t0001g0195a0001c0001t0001g0218a0001c0001t0001g0219 | 3 | HG02027.hp1 HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.46-24978G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77868630 | ||||||
| chr7:77868664
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-24944T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77868664 | ||||||
| chr7:77868806
|
T | G | 1 | a0001c0001t0001g0287 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.46-24802T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77868806 | ||||||
| chr7:77868851
|
C | G | 1 | a0001c0002t0013g0294 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.46-24757C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77868851 | ||||||
| chr7:77869073
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.46-24535C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77869073 | ||||||
| chr7:77869207
|
C | T | 1 | a0001c0002t0013g0294 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.46-24401C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77869207 | ||||||
| chr7:77869414
|
C | G | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.46-24194C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77869414 | ||||||
| chr7:77869588
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-24020T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77869588 | ||||||
| chr7:77869744
|
A | AC | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-23864_46-23863i others(3): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77869744 | ||||||
| chr7:77869816
|
T | G | 2 | a0001c0002t0013g0294a0001c0002t0020g0293 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.46-23792T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77869816 | ||||||
| chr7:77869943
|
G | GT | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01433.hp1 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-23658dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77869943 | |||||
| chr7:77870194
|
C | A | 58 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071others(55): Show | 58 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.46-23414C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77870194 | ||||||
| chr7:77870247
|
G | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0209 | 2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.46-23361G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77870247 | ||||||
| chr7:77870247
|
GT | G | 64 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(61): Show | 64 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.46-23347delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77870247 | |||||
| chr7:77870497
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.46-23111A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77870497 | ||||||
| chr7:77871044
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.46-22564C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77871044 | ||||||
| chr7:77871284
|
A | C | 78 | a0001c0001t0001g0056a0001c0001t0001g0302a0001c0001t0003g0306others(75): Show | 78 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.46-22324A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77871284 | ||||||
| chr7:77871380
|
A | C | 1 | a0001c0001t0001g0253 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.46-22228A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77871380 | ||||||
| chr7:77871383
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0135a0001c0001t0001g0174 | 3 | HG02293.hp2 NA18943.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.46-22225G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77871383 | ||||||
| chr7:77871417
|
T | C | 136 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 136 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.46-22191T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77871417 | ||||||
| chr7:77871666
|
GC | G | 65 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(62): Show | 65 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.46-21939delC | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77871666 | |||||
| chr7:77871712
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.46-21896G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77871712 | ||||||
| chr7:77871719
|
T | C | 68 | a0001c0001t0001g0056a0001c0001t0010g0072a0001c0001t0010g0073others(65): Show | 68 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.46-21889T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77871719 | ||||||
| chr7:77871903
|
G | T | 1 | a0001c0001t0001g0313 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.46-21705G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77871903 | ||||||
| chr7:77871980
|
T | C | 13 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(10): Show | 13 | HG01192.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.46-21628T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77871980 | ||||||
| chr7:77871990
|
G | A | 50 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.46-21618G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77871990 | ||||||
| chr7:77872007
|
A | G | 9 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(6): Show | 9 | HG01099.hp1 HG02055.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.46-21601A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77872007 | ||||||
| chr7:77872016
|
A | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01433.hp1 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-21592A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77872016 | ||||||
| chr7:77872371
|
A | G | 1 | a0001c0001t0008g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.46-21237A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77872371 | ||||||
| chr7:77872645
|
T | C | 62 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(59): Show | 62 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.46-20963T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77872645 | ||||||
| chr7:77872696
|
G | T | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-20912G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77872696 | ||||||
| chr7:77872732
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-20876T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77872732 | ||||||
| chr7:77872789
|
T | A | 1 | a0001c0001t0001g0129 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.46-20819T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77872789 | ||||||
| chr7:77872961
|
T | TG | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-20646dupG | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77872961 | |||||
| chr7:77873141
|
G | A | 78 | a0001c0001t0001g0056a0001c0001t0001g0302a0001c0001t0003g0306others(75): Show | 78 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.46-20467G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77873141 | ||||||
| chr7:77873163
|
G | A | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.46-20445G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77873163 | ||||||
| chr7:77873194
|
T | TGTAATCC others(4): Show |
10 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-20413_46-20412i others(13): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77873194 | |||||
| chr7:77873223
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-20385G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77873223 | ||||||
| chr7:77873237
|
T | C | 3 | a0001c0002t0002g0046a0001c0002t0002g0097a0001c0002t0002g0098 | 3 | HG00733.hp1 HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.46-20371T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77873237 | ||||||
| chr7:77873256
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-20352G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77873256 | ||||||
| chr7:77873411
|
T | G | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.46-20197T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77873411 | ||||||
| chr7:77873507
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.46-20101A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77873507 | ||||||
| chr7:77873640
|
G | A | 3 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG01071.hp1 HG01074.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.46-19968G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77873640 | ||||||
| chr7:77873717
|
C | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-19891C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77873717 | ||||||
| chr7:77873840
|
G | A | 4 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG00642.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-19768G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77873840 | ||||||
| chr7:77873900
|
T | C | 2 | a0001c0001t0010g0072a0001c0001t0010g0073 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.46-19708T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77873900 | ||||||
| chr7:77873953
|
A | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-19655A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77873953 | ||||||
| chr7:77874134
|
C | G | 1 | a0001c0002t0002g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.46-19474C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77874134 | ||||||
| chr7:77874401
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.46-19207A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77874401 | ||||||
| chr7:77874455
|
A | G | 1 | a0001c0002t0002g0070 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.46-19153A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77874455 | ||||||
| chr7:77874467
|
C | CA | 4 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG00639.hp2 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-19139dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77874467 | |||||
| chr7:77874523
|
C | T | 4 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG00639.hp2 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-19085C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77874523 | ||||||
| chr7:77874778
|
G | C | 214 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(211): Show | 214 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.46-18830G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77874778 | ||||||
| chr7:77875011
|
T | G | 2 | a0001c0002t0013g0294a0001c0002t0020g0293 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.46-18597T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77875011 | ||||||
| chr7:77875342
|
T | G | 3 | a0001c0004t0007g0017a0001c0004t0007g0069a0001c0004t0007g0277 | 3 | HG02572.hp1 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.46-18266T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77875342 | ||||||
| chr7:77875419
|
G | A | 33 | a0001c0001t0001g0302a0001c0001t0003g0306a0001c0001t0003g0307others(30): Show | 33 | HG00140.hp1 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.46-18189G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77875419 | ||||||
| chr7:77875525
|
A | G | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.46-18083A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77875525 | ||||||
| chr7:77875530
|
ATATT | A | 210 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(207): Show | 210 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.46-18053_46-18050d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77875530 | |||||
| chr7:77875578
|
C | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-18030C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77875578 | ||||||
| chr7:77875588
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.46-18020C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77875588 | ||||||
| chr7:77875599
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-18009C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77875599 | ||||||
| chr7:77875600
|
C | G | 1 | a0001c0001t0001g0100 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.46-18008C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77875600 | ||||||
| chr7:77875643
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.46-17965C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77875643 | ||||||
| chr7:77875917
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-17691A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77875917 | ||||||
| chr7:77875919
|
A | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-17689A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77875919 | ||||||
| chr7:77876067
|
G | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0102 | 2 | NA18962.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.46-17541G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77876067 | ||||||
| chr7:77876185
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.46-17423G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77876185 | ||||||
| chr7:77876303
|
A | C | 3 | a0001c0001t0001g0081a0001c0001t0005g0025a0001c0001t0005g0026 | 3 | HG02451.hp2 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.46-17305A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77876303 | ||||||
| chr7:77876340
|
G | A | 10 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-17268G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77876340 | ||||||
| chr7:77876409
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.46-17199G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77876409 | ||||||
| chr7:77876534
|
T | C | 4 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG00639.hp2 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-17074T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77876534 | ||||||
| chr7:77876671
|
T | A | 1 | a0001c0002t0002g0032 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.46-16937T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77876671 | ||||||
| chr7:77876921
|
A | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01433.hp1 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-16687A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77876921 | ||||||
| chr7:77877282
|
T | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-16326T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77877282 | ||||||
| chr7:77877325
|
C | T | 1 | a0001c0002t0002g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.46-16283C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77877325 | ||||||
| chr7:77877513
|
A | G | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.46-16095A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77877513 | ||||||
| chr7:77877678
|
A | G | 7 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(4): Show | 7 | HG01109.hp2 HG01433.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-15930A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77877678 | ||||||
| chr7:77877938
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-15670C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77877938 | ||||||
| chr7:77877942
|
TG | T | 5 | a0001c0001t0001g0227a0001c0001t0001g0254a0001c0001t0001g0255others(2): Show | 5 | HG00438.hp2 HG02071.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-15661delG | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77877942 | |||||
| chr7:77878129
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-15479G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77878129 | ||||||
| chr7:77878366
|
C | T | 2 | a0001c0002t0013g0294a0001c0002t0020g0293 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.46-15242C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77878366 | ||||||
| chr7:77878415
|
A | C | 3 | a0001c0001t0006g0265a0001c0001t0006g0296a0001c0001t0006g0300 | 3 | HG03579.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.46-15193A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77878415 | ||||||
| chr7:77878531
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-15077G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77878531 | ||||||
| chr7:77878973
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-14635G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77878973 | ||||||
| chr7:77879013
|
G | A | 3 | a0001c0004t0007g0017a0001c0004t0007g0069a0001c0004t0007g0277 | 3 | HG02572.hp1 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.46-14595G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77879013 | ||||||
| chr7:77879105
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.46-14503C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77879105 | ||||||
| chr7:77879111
|
A | G | 3 | a0001c0004t0007g0017a0001c0004t0007g0069a0001c0004t0007g0277 | 3 | HG02572.hp1 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.46-14497A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77879111 | ||||||
| chr7:77879247
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.46-14361C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77879247 | ||||||
| chr7:77879316
|
C | T | 91 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.46-14292C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77879316 | ||||||
| chr7:77879330
|
G | C | 62 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(59): Show | 62 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.46-14278G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77879330 | ||||||
| chr7:77879601
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0167 | 2 | HG01952.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.46-14007G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77879601 | ||||||
| chr7:77879673
|
T | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-13935T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77879673 | ||||||
| chr7:77879771
|
A | C | 62 | a0001c0001t0001g0056a0001c0001t0010g0072a0001c0001t0010g0073others(59): Show | 62 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.46-13837A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77879771 | ||||||
| chr7:77879771
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.46-13837A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77879771 | ||||||
| chr7:77879893
|
C | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-13715C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77879893 | ||||||
| chr7:77879950
|
T | G | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0136 | 3 | NA18960.hp2 NA19007.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.46-13658T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77879950 | ||||||
| chr7:77879990
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-13618G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77879990 | ||||||
| chr7:77880055
|
A | G | 10 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-13553A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77880055 | ||||||
| chr7:77880086
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.46-13522C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77880086 | ||||||
| chr7:77880120
|
T | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-13488T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77880120 | ||||||
| chr7:77880437
|
T | C | 2 | a0002c0005t0001g0189a0002c0005t0001g0190 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.46-13171T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77880437 | ||||||
| chr7:77880557
|
T | C | 214 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(211): Show | 214 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.46-13051T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77880557 | ||||||
| chr7:77880608
|
C | A | 62 | a0001c0001t0001g0056a0001c0001t0010g0072a0001c0001t0010g0073others(59): Show | 62 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.46-13000C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77880608 | ||||||
| chr7:77880667
|
C | A | 10 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0104others(7): Show | 10 | HG01099.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-12941C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77880667 | ||||||
| chr7:77880702
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030 | 3 | HG01433.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.46-12906C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77880702 | ||||||
| chr7:77880854
|
T | C | 1 | a0001c0001t0019g0066 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.46-12754T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77880854 | ||||||
| chr7:77880942
|
C | A | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-12666C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77880942 | ||||||
| chr7:77881040
|
G | A | 50 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.46-12568G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77881040 | ||||||
| chr7:77881301
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.46-12307C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77881301 | ||||||
| chr7:77881373
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-12235G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77881373 | ||||||
| chr7:77881380
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.46-12228A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77881380 | ||||||
| chr7:77881444
|
A | T | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.46-12164A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77881444 | ||||||
| chr7:77881515
|
G | GTT | 4 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-12090_46-12089d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77881515 | |||||
| chr7:77881519
|
TG | T | 65 | a0001c0001t0001g0056a0001c0001t0010g0072a0001c0001t0010g0073others(62): Show | 65 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.46-12088delG | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77881519 | ||||||
| chr7:77881520
|
G | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-12088G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77881520 | ||||||
| chr7:77881520
|
GT | G | 156 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(153): Show | 156 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.46-12076delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77881520 | |||||
| chr7:77881568
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-12040G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77881568 | ||||||
| chr7:77881583
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-12025T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77881583 | ||||||
| chr7:77881677
|
C | A | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.46-11931C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77881677 | ||||||
| chr7:77881889
|
A | C | 1 | a0001c0001t0001g0210 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.46-11719A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77881889 | ||||||
| chr7:77882069
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.46-11539C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77882069 | ||||||
| chr7:77882085
|
G | A | 1 | a0001c0002t0002g0065 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.46-11523G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77882085 | ||||||
| chr7:77882174
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.46-11434C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77882174 | ||||||
| chr7:77882177
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-11431T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77882177 | ||||||
| chr7:77882246
|
T | G | 1 | a0001c0001t0001g0018 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.46-11362T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77882246 | ||||||
| chr7:77882313
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-11295C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77882313 | ||||||
| chr7:77882356
|
TA | T | 55 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 55 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.46-11239delA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77882356 | |||||
| chr7:77882370
|
T | A | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-11238T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77882370 | ||||||
| chr7:77882531
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-11077A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77882531 | ||||||
| chr7:77882781
|
G | C | 132 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(129): Show | 132 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.46-10827G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77882781 | ||||||
| chr7:77882908
|
T | G | 1 | a0001c0003t0004g0003 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.46-10700T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77882908 | ||||||
| chr7:77882969
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-10639A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77882969 | ||||||
| chr7:77883046
|
A | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-10562A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77883046 | ||||||
| chr7:77883271
|
C | G | 7 | a0001c0001t0001g0122a0001c0001t0001g0128a0001c0001t0001g0137others(4): Show | 7 | HG00621.hp2 HG01952.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-10337C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77883271 | ||||||
| chr7:77883433
|
T | A | 1 | a0001c0001t0001g0204 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.46-10175T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77883433 | ||||||
| chr7:77883488
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.46-10120C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77883488 | ||||||
| chr7:77883508
|
C | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG00280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.46-10100C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77883508 | ||||||
| chr7:77883704
|
G | A | 1 | a0001c0002t0002g0067 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.46-9904G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77883704 | ||||||
| chr7:77883946
|
T | C | 1 | a0001c0001t0003g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.46-9662T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77883946 | ||||||
| chr7:77884163
|
G | A | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.46-9445G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77884163 | ||||||
| chr7:77884165
|
AC | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0193a0001c0001t0001g0194others(4): Show | 7 | HG02071.hp1 HG02080.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-9442delC | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77884165 | ||||||
| chr7:77884287
|
A | C | 1 | a0001c0001t0001g0140 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.46-9321A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77884287 | ||||||
| chr7:77884431
|
A | G | 9 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(6): Show | 9 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-9177A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77884431 | ||||||
| chr7:77884568
|
T | C | 214 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(211): Show | 214 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.46-9040T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77884568 | ||||||
| chr7:77884577
|
G | A | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-9031G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77884577 | ||||||
| chr7:77884646
|
C | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030 | 3 | HG01433.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.46-8962C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77884646 | ||||||
| chr7:77884853
|
C | T | 1 | a0001c0002t0001g0289 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.46-8755C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77884853 | ||||||
| chr7:77884886
|
G | A | 1 | a0001c0002t0002g0065 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.46-8722G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77884886 | ||||||
| chr7:77884899
|
A | AAAAT | 24 | a0001c0001t0001g0091a0001c0001t0001g0175a0001c0001t0001g0178others(21): Show | 24 | HG00280.hp2 HG00323.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.46-8685_46-8682dup others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77884899 | |||||
| chr7:77884899
|
A | AAAATAAA others(1): Show |
28 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(25): Show | 28 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.46-8689_46-8682dup others(8): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77884899 | |||||
| chr7:77884899
|
A | AAAATAAA others(5): Show |
2 | a0001c0001t0001g0088a0001c0001t0001g0196 | 2 | HG03654.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.46-8693_46-8682dup others(12): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77884899 | |||||
| chr7:77884899
|
AAAATAAA others(1): Show |
A | 69 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(66): Show | 69 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.46-8689_46-8682del others(8): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77884899 | |||||
| chr7:77885002
|
C | T | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.46-8606C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77885002 | ||||||
| chr7:77885072
|
A | C | 214 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(211): Show | 214 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.46-8536A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77885072 | ||||||
| chr7:77885080
|
T | A | 1 | a0001c0001t0001g0164 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.46-8528T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77885080 | ||||||
| chr7:77885126
|
T | C | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG00280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.46-8482T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77885126 | ||||||
| chr7:77885161
|
A | G | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | NA19066.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.46-8447A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77885161 | ||||||
| chr7:77885355
|
G | A | 1 | a0001c0002t0002g0032 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.46-8253G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77885355 | ||||||
| chr7:77885440
|
A | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(3): Show | 6 | HG01433.hp1 HG02630.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-8168A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77885440 | ||||||
| chr7:77885450
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-8158T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77885450 | ||||||
| chr7:77885491
|
C | A | 1 | a0001c0001t0001g0119 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.46-8117C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77885491 | ||||||
| chr7:77885530
|
C | T | 61 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071others(58): Show | 61 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.46-8078C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77885530 | ||||||
| chr7:77885662
|
C | G | 1 | a0001c0001t0001g0235 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.46-7946C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77885662 | ||||||
| chr7:77885873
|
T | C | 57 | a0001c0001t0001g0056a0001c0001t0010g0072a0001c0001t0010g0073others(54): Show | 57 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.46-7735T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77885873 | ||||||
| chr7:77886105
|
A | T | 69 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(66): Show | 69 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.46-7503A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77886105 | ||||||
| chr7:77886107
|
C | T | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-7501C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77886107 | ||||||
| chr7:77886257
|
T | G | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.46-7351T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77886257 | ||||||
| chr7:77886322
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.46-7286A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77886322 | ||||||
| chr7:77886574
|
G | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0173 | 2 | NA18945.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.46-7034G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77886574 | ||||||
| chr7:77886632
|
T | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0152 | 2 | HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.46-6976T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77886632 | ||||||
| chr7:77886768
|
G | C | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-6840G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77886768 | ||||||
| chr7:77887027
|
C | A | 69 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(66): Show | 69 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.46-6581C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77887027 | ||||||
| chr7:77887038
|
CCT | C | 50 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.46-6569_46-6568del others(2): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77887038 | ||||||
| chr7:77887046
|
TA | T | 145 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(142): Show | 145 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.46-6546delA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77887046 | |||||
| chr7:77887061
|
A | C | 1 | a0001c0001t0001g0261 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.46-6547A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77887061 | ||||||
| chr7:77887101
|
G | T | 1 | a0001c0001t0001g0261 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.46-6507G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77887101 | ||||||
| chr7:77887175
|
TATATATT others(3): Show |
T | 3 | a0001c0004t0007g0017a0001c0004t0007g0069a0001c0004t0007g0277 | 3 | HG02572.hp1 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.46-6423_46-6414del others(10): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77887175 | |||||
| chr7:77887208
|
G | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01433.hp1 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-6400G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77887208 | ||||||
| chr7:77887222
|
A | C | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-6386A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77887222 | ||||||
| chr7:77887246
|
T | A | 1 | a0001c0001t0001g0261 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.46-6362T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77887246 | ||||||
| chr7:77887343
|
G | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0297 | 2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.46-6265G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77887343 | ||||||
| chr7:77887355
|
C | CT | 7 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(4): Show | 7 | HG01109.hp2 HG01433.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-6242dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77887355 | |||||
| chr7:77887426
|
G | T | 77 | a0001c0001t0001g0302a0001c0001t0003g0306a0001c0001t0003g0307others(74): Show | 77 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.46-6182G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77887426 | ||||||
| chr7:77887567
|
C | T | 61 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071others(58): Show | 61 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.46-6041C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77887567 | ||||||
| chr7:77887624
|
C | G | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-5984C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77887624 | ||||||
| chr7:77887747
|
A | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-5861A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77887747 | ||||||
| chr7:77888150
|
T | C | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG00621.hp1 NA18983.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-5458T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77888150 | ||||||
| chr7:77888192
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-5416G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77888192 | ||||||
| chr7:77888208
|
G | A | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.46-5400G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77888208 | ||||||
| chr7:77888337
|
A | G | 1 | a0001c0002t0002g0070 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.46-5271A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77888337 | ||||||
| chr7:77888403
|
G | A | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0198others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-5205G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77888403 | ||||||
| chr7:77888477
|
G | A | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-5131G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77888477 | ||||||
| chr7:77888510
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.46-5098T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77888510 | ||||||
| chr7:77888802
|
C | T | 7 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(4): Show | 7 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-4806C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77888802 | ||||||
| chr7:77888860
|
T | TA | 61 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(58): Show | 61 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.46-4737dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77888860 | |||||
| chr7:77888985
|
A | G | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.46-4623A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77888985 | ||||||
| chr7:77889048
|
C | T | 1 | a0001c0001t0018g0160 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.46-4560C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77889048 | ||||||
| chr7:77889437
|
A | G | 2 | a0001c0004t0007g0017a0001c0004t0007g0069 | 2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.46-4171A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77889437 | ||||||
| chr7:77889478
|
C | T | 7 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(4): Show | 7 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-4130C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77889478 | ||||||
| chr7:77889497
|
C | T | 1 | a0001c0001t0005g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.46-4111C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77889497 | ||||||
| chr7:77889514
|
T | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-4094T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77889514 | ||||||
| chr7:77889515
|
A | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-4093A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77889515 | ||||||
| chr7:77889516
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-4092C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77889516 | ||||||
| chr7:77889517
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46-4091C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77889517 | ||||||
| chr7:77889577
|
C | CT | 12 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(9): Show | 12 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.46-4016dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77889577 | |||||
| chr7:77889577
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.46-4031C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77889577 | ||||||
| chr7:77889593
|
C | T | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.46-4015C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77889593 | ||||||
| chr7:77889594
|
C | CT | 10 | a0001c0001t0001g0100a0001c0001t0001g0295a0001c0001t0001g0298others(7): Show | 10 | HG01099.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.46-3999dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77889594 | |||||
| chr7:77889594
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-4014C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77889594 | ||||||
| chr7:77889595
|
T | C | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.46-4013T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77889595 | ||||||
| chr7:77889764
|
T | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0117a0001c0001t0001g0137others(1): Show | 4 | HG01517.hp1 HG02738.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-3844T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77889764 | ||||||
| chr7:77889932
|
G | A | 1 | a0001c0002t0002g0070 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.46-3676G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77889932 | ||||||
| chr7:77889946
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030 | 3 | HG01433.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.46-3662C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77889946 | ||||||
| chr7:77890021
|
C | T | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(1): Show | 4 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-3587C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77890021 | ||||||
| chr7:77890022
|
G | GC | 132 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0018others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.46-3577dupC | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77890022 | |||||
| chr7:77890022
|
G | GCC | 20 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0088others(17): Show | 20 | HG00642.hp2 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.46-3578_46-3577dup others(2): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77890022 | |||||
| chr7:77890101
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.46-3507G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77890101 | ||||||
| chr7:77890197
|
G | T | 1 | a0001c0001t0001g0274 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.46-3411G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77890197 | ||||||
| chr7:77890577
|
G | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-3031G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77890577 | ||||||
| chr7:77890599
|
C | CT | 84 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(81): Show | 84 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.46-2985dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77890599 | |||||
| chr7:77890599
|
C | CTT | 14 | a0001c0001t0001g0165a0001c0001t0001g0219a0001c0001t0001g0248others(11): Show | 14 | HG00639.hp2 HG01175.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.46-2986_46-2985dup others(2): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77890599 | |||||
| chr7:77890599
|
CT | C | 21 | a0001c0001t0001g0018a0001c0001t0001g0086a0001c0001t0001g0106others(18): Show | 21 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.46-2985delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77890599 | |||||
| chr7:77890698
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.46-2910C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77890698 | ||||||
| chr7:77890904
|
C | CT | 72 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(69): Show | 72 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.46-2682dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77890904 | |||||
| chr7:77890904
|
C | CTT | 10 | a0001c0001t0001g0092a0001c0001t0001g0179a0001c0001t0001g0188others(7): Show | 10 | HG00642.hp2 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-2683_46-2682dup others(2): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77890904 | |||||
| chr7:77891000
|
T | C | 1 | a0001c0001t0023g0278 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.46-2608T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77891000 | ||||||
| chr7:77891053
|
G | A | 22 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.46-2555G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77891053 | ||||||
| chr7:77891313
|
T | C | 1 | a0001c0001t0005g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.46-2295T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77891313 | ||||||
| chr7:77891417
|
TACC | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01109.hp2 HG01433.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-2189_46-2187del others(3): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77891417 | |||||
| chr7:77891421
|
A | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-2187A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77891421 | ||||||
| chr7:77891423
|
TAGGACTA others(3): Show |
T | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01109.hp2 HG01433.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-2182_46-2173del others(10): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77891423 | |||||
| chr7:77891437
|
T | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01109.hp2 HG01433.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-2171T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77891437 | ||||||
| chr7:77891438
|
G | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01109.hp2 HG01433.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-2170G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77891438 | ||||||
| chr7:77891503
|
A | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-2105A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77891503 | ||||||
| chr7:77891515
|
T | TTTGGTCT others(7): Show |
63 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071others(60): Show | 63 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.46-2081_46-2068dup others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77891515 | |||||
| chr7:77891578
|
T | TTTGTTG | 213 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(210): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.46-2028_46-2027ins others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 77891578 | |||||
| chr7:77891581
|
T | G | 304 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(301): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.46-2027T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77891581 | ||||||
| chr7:77891839
|
A | G | 1 | a0001c0001t0005g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.46-1769A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77891839 | ||||||
| chr7:77891878
|
G | C | 5 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0181others(2): Show | 5 | HG02818.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-1730G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77891878 | ||||||
| chr7:77891885
|
G | A | 6 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-1723G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77891885 | ||||||
| chr7:77891999
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.46-1609C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77891999 | ||||||
| chr7:77892063
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.46-1545G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77892063 | ||||||
| chr7:77892084
|
T | G | 1 | a0001c0002t0002g0034 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.46-1524T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77892084 | ||||||
| chr7:77892160
|
C | T | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.46-1448C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77892160 | ||||||
| chr7:77892364
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.46-1244A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77892364 | ||||||
| chr7:77892630
|
A | G | 79 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(76): Show | 79 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.46-978A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77892630 | ||||||
| chr7:77892680
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.46-928A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77892680 | ||||||
| chr7:77892868
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.46-740T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77892868 | ||||||
| chr7:77892931
|
G | A | 2 | a0001c0002t0013g0294a0001c0002t0020g0293 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.46-677G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77892931 | ||||||
| chr7:77893003
|
T | A | 1 | a0001c0001t0005g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.46-605T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77893003 | ||||||
| chr7:77893107
|
T | C | 1 | a0001c0002t0002g0036 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.46-501T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77893107 | ||||||
| chr7:77893152
|
A | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0209 | 2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.46-456A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77893152 | ||||||
| chr7:77893178
|
A | T | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-430A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77893178 | ||||||
| chr7:77893199
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.46-409G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77893199 | ||||||
| chr7:77893254
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.46-354T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77893254 | ||||||
| chr7:77893409
|
A | G | 1 | a0001c0002t0002g0288 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.46-199A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 2/18 | chr7 | 77893409 | ||||||
| chr7:77893718
|
A | G | 62 | a0001c0001t0001g0056a0001c0001t0010g0072a0001c0001t0010g0073others(59): Show | 62 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.102+54A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 3/18 | chr7 | 77893718 | ||||||
| chr7:77893905
|
T | C | 3 | a0001c0004t0007g0017a0001c0004t0007g0069a0001c0004t0007g0277 | 3 | HG02572.hp1 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.103-77T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 3/18 | chr7 | 77893905 | ||||||
| chr7:77894096
|
C | T | 1 | a0001c0001t0005g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.114+103C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77894096 | ||||||
| chr7:77894097
|
G | A | 4 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG00642.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+104G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77894097 | ||||||
| chr7:77894200
|
T | C | 1 | a0001c0002t0002g0047 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.114+207T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77894200 | ||||||
| chr7:77894204
|
A | G | 214 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(211): Show | 214 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.114+211A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77894204 | ||||||
| chr7:77894228
|
T | C | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00423.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.114+235T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77894228 | ||||||
| chr7:77894387
|
C | T | 62 | a0001c0001t0001g0056a0001c0001t0010g0072a0001c0001t0010g0073others(59): Show | 62 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.114+394C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77894387 | ||||||
| chr7:77894388
|
C | T | 214 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(211): Show | 214 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.114+395C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77894388 | ||||||
| chr7:77894452
|
A | G | 136 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(133): Show | 136 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.114+459A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77894452 | ||||||
| chr7:77894883
|
T | A | 7 | a0001c0001t0001g0295a0001c0001t0001g0298a0001c0001t0001g0299others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+890T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77894883 | ||||||
| chr7:77895090
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.114+1097A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77895090 | ||||||
| chr7:77895372
|
A | C | 71 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(68): Show | 71 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.114+1379A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77895372 | ||||||
| chr7:77895877
|
T | G | 69 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(66): Show | 69 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.114+1884T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77895877 | ||||||
| chr7:77895882
|
T | C | 214 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(211): Show | 214 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.114+1889T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77895882 | ||||||
| chr7:77895907
|
C | T | 2 | a0001c0001t0003g0307a0001c0001t0003g0308 | 2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.114+1914C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77895907 | ||||||
| chr7:77895940
|
G | C | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.114+1947G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77895940 | ||||||
| chr7:77895963
|
T | C | 4 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG00639.hp2 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+1970T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77895963 | ||||||
| chr7:77896070
|
A | C | 79 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(76): Show | 79 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.114+2077A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77896070 | ||||||
| chr7:77896097
|
A | G | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.114+2104A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77896097 | ||||||
| chr7:77896218
|
A | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.114+2225A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77896218 | ||||||
| chr7:77896390
|
T | TA | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+2407dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr7 | 77896390 | |||||
| chr7:77896478
|
C | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0129a0001c0001t0001g0140 | 3 | HG03491.hp1 HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.114+2485C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77896478 | ||||||
| chr7:77896487
|
G | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01109.hp2 HG01433.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+2494G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77896487 | ||||||
| chr7:77896679
|
G | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01109.hp2 HG01433.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+2686G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77896679 | ||||||
| chr7:77896737
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.114+2744G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77896737 | ||||||
| chr7:77896949
|
T | C | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+2956T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77896949 | ||||||
| chr7:77897131
|
A | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.114+3138A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77897131 | ||||||
| chr7:77897293
|
A | AT | 199 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.114+3318dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr7 | 77897293 | |||||
| chr7:77897293
|
A | ATT | 29 | a0001c0001t0001g0084a0001c0001t0001g0103a0001c0001t0001g0115others(26): Show | 29 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.114+3317_114+3318d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr7 | 77897293 | |||||
| chr7:77897293
|
A | T | 1 | a0001c0001t0001g0225 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.114+3300A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77897293 | ||||||
| chr7:77897468
|
G | A | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.115-3243G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77897468 | ||||||
| chr7:77897503
|
A | C | 1 | a0001c0002t0002g0098 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.115-3208A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77897503 | ||||||
| chr7:77897675
|
A | T | 52 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(49): Show | 52 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.115-3036A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77897675 | ||||||
| chr7:77897784
|
G | A | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.115-2927G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77897784 | ||||||
| chr7:77897969
|
AC | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 4 | HG00099.hp2 HG01109.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-2740delC | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr7 | 77897969 | |||||
| chr7:77897986
|
G | GT | 66 | a0001c0001t0001g0056a0001c0001t0010g0072a0001c0001t0010g0073others(63): Show | 66 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.115-2711dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr7 | 77897986 | |||||
| chr7:77898064
|
T | C | 7 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(4): Show | 7 | HG01109.hp2 HG01433.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-2647T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77898064 | ||||||
| chr7:77898082
|
C | A | 1 | a0001c0002t0002g0047 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.115-2629C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77898082 | ||||||
| chr7:77898102
|
A | G | 1 | a0001c0001t0001g0264 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.115-2609A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77898102 | ||||||
| chr7:77898139
|
A | G | 98 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.115-2572A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77898139 | ||||||
| chr7:77898252
|
A | T | 3 | a0001c0002t0002g0037a0001c0002t0002g0045a0001c0002t0002g0051 | 3 | NA18969.hp1 NA19062.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.115-2459A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77898252 | ||||||
| chr7:77898620
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.115-2091C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77898620 | ||||||
| chr7:77898779
|
CTTTA | C | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-1912_115-1909d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr7 | 77898779 | |||||
| chr7:77898878
|
A | G | 1 | a0001c0001t0008g0145 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.115-1833A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77898878 | ||||||
| chr7:77898990
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.115-1721C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77898990 | ||||||
| chr7:77899295
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.115-1416G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77899295 | ||||||
| chr7:77899341
|
G | A | 3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0282 | 3 | HG02647.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.115-1370G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77899341 | ||||||
| chr7:77899354
|
A | AT | 6 | a0001c0001t0001g0292a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-1345dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr7 | 77899354 | |||||
| chr7:77899902
|
T | A | 56 | a0001c0001t0001g0056a0001c0001t0010g0072a0001c0001t0010g0073others(53): Show | 56 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.115-809T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77899902 | ||||||
| chr7:77899959
|
A | T | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.115-752A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77899959 | ||||||
| chr7:77900131
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-580A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77900131 | ||||||
| chr7:77900201
|
C | T | 4 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-510C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77900201 | ||||||
| chr7:77900247
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.115-464G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77900247 | ||||||
| chr7:77900430
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.115-281C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77900430 | ||||||
| chr7:77900445
|
A | G | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.115-266A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77900445 | ||||||
| chr7:77900550
|
A | G | 1 | a0001c0002t0002g0038 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.115-161A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77900550 | ||||||
| chr7:77900567
|
T | C | 244 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(241): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.115-144T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 4/18 | chr7 | 77900567 | ||||||
| chr7:77900917
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.184+137A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 5/18 | chr7 | 77900917 | ||||||
| chr7:77900998
|
A | G | 3 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071 | 3 | HG02257.hp2 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.184+218A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 5/18 | chr7 | 77900998 | ||||||
| chr7:77901026
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.184+246G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 5/18 | chr7 | 77901026 | ||||||
| chr7:77901046
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.184+266A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 5/18 | chr7 | 77901046 | ||||||
| chr7:77901053
|
A | G | 3 | a0001c0001t0001g0121a0001c0001t0001g0135a0001c0001t0001g0174 | 3 | HG02293.hp2 NA18943.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.184+273A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 5/18 | chr7 | 77901053 | ||||||
| chr7:77901096
|
G | C | 9 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0274others(6): Show | 9 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.184+316G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 5/18 | chr7 | 77901096 | ||||||
| chr7:77901203
|
T | G | 1 | a0001c0002t0022g0080 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.184+423T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 5/18 | chr7 | 77901203 | ||||||
| chr7:77901226
|
A | G | 1 | a0001c0001t0005g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.184+446A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 5/18 | chr7 | 77901226 | ||||||
| chr7:77901261
|
ATCTG | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030 | 3 | HG01433.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.184+489_185-490del others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 77901261 | |||||
| chr7:77901324
|
T | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.185-438T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 5/18 | chr7 | 77901324 | ||||||
| chr7:77901457
|
C | CAACA | 250 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.185-282_185-279dup others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 77901457 | |||||
| chr7:77901457
|
C | CAACAAAC others(1): Show |
5 | a0001c0001t0003g0306a0001c0001t0003g0309a0001c0001t0003g0310others(2): Show | 5 | HG02055.hp2 HG02559.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.185-286_185-279dup others(8): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 77901457 | |||||
| chr7:77901457
|
CAACA | C | 54 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(51): Show | 54 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.185-282_185-279del others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 77901457 | |||||
| chr7:77901633
|
T | C | 11 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(8): Show | 11 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.185-129T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 5/18 | chr7 | 77901633 | ||||||
| chr7:77902027
|
G | A | 4 | a0001c0001t0001g0168a0001c0001t0001g0172a0001c0001t0008g0124others(1): Show | 4 | HG00438.hp1 HG02015.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.343+107G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77902027 | ||||||
| chr7:77902076
|
AAAC | A | 53 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(50): Show | 53 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.343+159_343+161del others(3): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 77902076 | |||||
| chr7:77902110
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.343+190A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77902110 | ||||||
| chr7:77902412
|
A | G | 1 | a0001c0002t0002g0061 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.343+492A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77902412 | ||||||
| chr7:77902643
|
A | G | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0198others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.343+723A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77902643 | ||||||
| chr7:77902646
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.343+726C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77902646 | ||||||
| chr7:77902719
|
A | T | 10 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.343+799A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77902719 | ||||||
| chr7:77902731
|
C | A | 1 | a0001c0002t0002g0035 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.343+811C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77902731 | ||||||
| chr7:77902832
|
A | G | 53 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(50): Show | 53 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.343+912A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77902832 | ||||||
| chr7:77902968
|
A | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.343+1048A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77902968 | ||||||
| chr7:77903204
|
A | C | 99 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0074others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.343+1284A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77903204 | ||||||
| chr7:77903368
|
T | C | 10 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.343+1448T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77903368 | ||||||
| chr7:77903487
|
A | G | 7 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(4): Show | 7 | HG01109.hp2 HG01433.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.343+1567A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77903487 | ||||||
| chr7:77903571
|
A | G | 2 | a0001c0002t0002g0038a0001c0002t0002g0054 | 2 | NA18943.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.343+1651A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77903571 | ||||||
| chr7:77903583
|
G | A | 50 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.343+1663G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77903583 | ||||||
| chr7:77903939
|
T | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.343+2019T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77903939 | ||||||
| chr7:77904006
|
T | C | 12 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.343+2086T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77904006 | ||||||
| chr7:77904080
|
A | G | 53 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(50): Show | 53 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.343+2160A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77904080 | ||||||
| chr7:77904190
|
A | G | 2 | a0001c0002t0002g0097a0001c0002t0002g0098 | 2 | HG00733.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.343+2270A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77904190 | ||||||
| chr7:77904362
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.343+2442G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77904362 | ||||||
| chr7:77904763
|
G | A | 1 | a0001c0001t0012g0303 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.343+2843G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77904763 | ||||||
| chr7:77904868
|
A | G | 1 | a0001c0001t0001g0232 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.343+2948A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77904868 | ||||||
| chr7:77904988
|
G | T | 1 | a0001c0001t0001g0087 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.343+3068G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77904988 | ||||||
| chr7:77904997
|
T | A | 62 | a0001c0001t0001g0135a0001c0001t0001g0302a0001c0002t0001g0289others(59): Show | 62 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.343+3077T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77904997 | ||||||
| chr7:77905246
|
C | T | 12 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.343+3326C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77905246 | ||||||
| chr7:77905322
|
C | T | 20 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(17): Show | 20 | HG00280.hp2 HG00323.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.343+3402C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77905322 | ||||||
| chr7:77905323
|
A | G | 3 | a0001c0004t0007g0017a0001c0004t0007g0069a0001c0004t0007g0277 | 3 | HG02572.hp1 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.343+3403A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77905323 | ||||||
| chr7:77905327
|
A | G | 22 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(19): Show | 22 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.343+3407A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77905327 | ||||||
| chr7:77905387
|
A | T | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.344-3406A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77905387 | ||||||
| chr7:77905441
|
A | G | 1 | a0001c0002t0002g0216 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.344-3352A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77905441 | ||||||
| chr7:77905553
|
C | T | 1 | a0001c0001t0005g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.344-3240C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77905553 | ||||||
| chr7:77905558
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.344-3235G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77905558 | ||||||
| chr7:77905605
|
C | A | 1 | a0001c0001t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.344-3188C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77905605 | ||||||
| chr7:77905694
|
C | T | 20 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(17): Show | 20 | HG00280.hp2 HG00323.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.344-3099C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77905694 | ||||||
| chr7:77905744
|
C | T | 1 | a0001c0001t0021g0312 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.344-3049C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77905744 | ||||||
| chr7:77906179
|
G | A | 68 | a0001c0001t0001g0016a0001c0001t0001g0075a0001c0001t0001g0076others(65): Show | 68 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.344-2614G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77906179 | ||||||
| chr7:77906232
|
G | A | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.344-2561G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77906232 | ||||||
| chr7:77906281
|
C | T | 28 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(25): Show | 28 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.344-2512C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77906281 | ||||||
| chr7:77906767
|
G | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0126 | 2 | NA18988.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.344-2026G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77906767 | ||||||
| chr7:77906855
|
C | T | 61 | a0001c0001t0001g0261a0001c0002t0001g0289a0001c0002t0002g0008others(58): Show | 61 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.344-1938C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77906855 | ||||||
| chr7:77906898
|
A | G | 17 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.344-1895A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77906898 | ||||||
| chr7:77906901
|
C | T | 1 | a0001c0002t0002g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.344-1892C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77906901 | ||||||
| chr7:77906934
|
T | TA | 70 | a0001c0001t0001g0111a0001c0001t0001g0218a0001c0001t0001g0220others(67): Show | 70 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.344-1841dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 77906934 | |||||
| chr7:77906934
|
T | TAA | 103 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.344-1842_344-1841d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 77906934 | |||||
| chr7:77906934
|
T | TAAA | 14 | a0001c0001t0001g0078a0001c0001t0001g0100a0001c0001t0001g0131others(11): Show | 14 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.344-1843_344-1841d others(5): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 77906934 | |||||
| chr7:77907494
|
C | A | 3 | a0001c0004t0007g0017a0001c0004t0007g0069a0001c0004t0007g0277 | 3 | HG02572.hp1 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.344-1299C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77907494 | ||||||
| chr7:77907800
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.344-993G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77907800 | ||||||
| chr7:77907878
|
C | G | 6 | a0001c0001t0001g0078a0001c0001t0001g0106a0001c0001t0001g0107others(3): Show | 6 | HG00735.hp2 HG01255.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-915C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77907878 | ||||||
| chr7:77908056
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.344-737A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77908056 | ||||||
| chr7:77908085
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.344-708C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77908085 | ||||||
| chr7:77908256
|
G | A | 39 | a0001c0002t0002g0021a0001c0002t0002g0022a0001c0002t0002g0028others(36): Show | 39 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.344-537G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77908256 | ||||||
| chr7:77908468
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.344-325G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77908468 | ||||||
| chr7:77908552
|
G | C | 2 | a0001c0002t0002g0049a0001c0002t0002g0050 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.344-241G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77908552 | ||||||
| chr7:77908586
|
G | C | 50 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.344-207G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77908586 | ||||||
| chr7:77908647
|
G | A | 234 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(231): Show | 234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.344-146G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 6/18 | chr7 | 77908647 | ||||||
| chr7:77909378
|
G | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01433.hp1 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+420G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 7/18 | chr7 | 77909378 | ||||||
| chr7:77909606
|
G | A | 1 | a0001c0001t0005g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.510-639G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 7/18 | chr7 | 77909606 | ||||||
| chr7:77909670
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.510-575T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 7/18 | chr7 | 77909670 | ||||||
| chr7:77909776
|
G | A | 50 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.510-469G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 7/18 | chr7 | 77909776 | ||||||
| chr7:77909976
|
T | C | 1 | a0001c0002t0002g0058 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.510-269T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 7/18 | chr7 | 77909976 | ||||||
| chr7:77910024
|
C | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.510-221C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 7/18 | chr7 | 77910024 | ||||||
| chr7:77910121
|
A | G | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.510-124A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 7/18 | chr7 | 77910121 | ||||||
| chr7:77910427
|
G | A | 99 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0074others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.674+18G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77910427 | ||||||
| chr7:77910434
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.674+25A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77910434 | ||||||
| chr7:77910579
|
T | C | 1 | a0001c0002t0002g0070 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.674+170T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77910579 | ||||||
| chr7:77910658
|
T | C | 1 | a0001c0004t0007g0277 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.674+249T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77910658 | ||||||
| chr7:77910697
|
A | G | 1 | a0001c0002t0022g0080 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.674+288A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77910697 | ||||||
| chr7:77910728
|
A | G | 50 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.674+319A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77910728 | ||||||
| chr7:77910766
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.674+357C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77910766 | ||||||
| chr7:77910767
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.674+358G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77910767 | ||||||
| chr7:77910804
|
G | A | 1 | a0001c0002t0002g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.674+395G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77910804 | ||||||
| chr7:77910805
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.674+396C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77910805 | ||||||
| chr7:77910808
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.674+399A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77910808 | ||||||
| chr7:77910819
|
T | G | 6 | a0001c0001t0001g0078a0001c0001t0001g0106a0001c0001t0001g0107others(3): Show | 6 | HG00735.hp2 HG01255.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.674+410T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77910819 | ||||||
| chr7:77911004
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG00423.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.674+595G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77911004 | ||||||
| chr7:77911014
|
A | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.674+605A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77911014 | ||||||
| chr7:77911017
|
T | C | 1 | a0004c0007t0001g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.674+608T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77911017 | ||||||
| chr7:77911062
|
A | G | 1 | a0001c0002t0002g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.674+653A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77911062 | ||||||
| chr7:77911141
|
T | A | 1 | a0001c0001t0001g0206 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.674+732T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77911141 | ||||||
| chr7:77911173
|
T | TACTATAC others(21): Show |
6 | a0001c0001t0001g0144a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.674+867_674+894dup others(28): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77911173 | |||||
| chr7:77911173
|
TACTATAC others(21): Show |
T | 49 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(46): Show | 49 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.674+867_674+894del others(28): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77911173 | |||||
| chr7:77911245
|
C | G | 1 | a0001c0001t0001g0056 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.674+836C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77911245 | ||||||
| chr7:77911680
|
G | A | 17 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.674+1271G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77911680 | ||||||
| chr7:77911803
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0209 | 2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.674+1394G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77911803 | ||||||
| chr7:77911926
|
A | G | 1 | a0001c0001t0005g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.674+1517A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77911926 | ||||||
| chr7:77912014
|
A | T | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.674+1605A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77912014 | ||||||
| chr7:77912015
|
T | A | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.674+1606T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77912015 | ||||||
| chr7:77912130
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.674+1721G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77912130 | ||||||
| chr7:77912356
|
G | A | 244 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(241): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.674+1947G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77912356 | ||||||
| chr7:77912429
|
C | T | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.674+2020C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77912429 | ||||||
| chr7:77912661
|
G | GTA | 61 | a0001c0001t0001g0056a0001c0002t0001g0289a0001c0002t0002g0008others(58): Show | 61 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.674+2264_674+2265d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912661 | |||||
| chr7:77912710
|
C | CT | 13 | a0001c0001t0001g0015a0001c0001t0001g0118a0001c0001t0001g0148others(10): Show | 13 | HG00733.hp2 HG01952.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.674+2340dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912710
|
C | CTT | 6 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0218others(3): Show | 6 | HG02738.hp2 HG03669.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.674+2339_674+2340d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912710
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0245 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.674+2330_674+2340d others(13): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912710
|
CT | C | 32 | a0001c0001t0001g0016a0001c0001t0001g0077a0001c0001t0001g0102others(29): Show | 32 | HG00323.hp1 HG00621.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.674+2340delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912710
|
CTT | C | 40 | a0001c0001t0001g0020a0001c0001t0001g0078a0001c0001t0001g0103others(37): Show | 40 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.674+2339_674+2340d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912710
|
CTTT | C | 16 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0122others(13): Show | 16 | HG00099.hp2 HG01070.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.674+2338_674+2340d others(5): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912710
|
CTTTT | C | 6 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0310others(3): Show | 6 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.674+2337_674+2340d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912710
|
CTTTTTTT | C | 9 | a0001c0001t0001g0024a0001c0001t0001g0295a0001c0001t0001g0297others(6): Show | 9 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.674+2334_674+2340d others(9): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912710
|
CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0266others(6): Show | 9 | HG00639.hp2 HG01109.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.674+2333_674+2340d others(10): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912710
|
CTTTTTTT others(2): Show |
C | 9 | a0001c0001t0001g0089a0001c0001t0001g0192a0001c0001t0001g0280others(6): Show | 9 | HG01256.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.674+2332_674+2340d others(11): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912710
|
CTTTTTTT others(3): Show |
C | 15 | a0001c0001t0001g0090a0001c0001t0001g0180a0001c0001t0001g0181others(12): Show | 15 | HG00140.hp1 HG00642.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.674+2331_674+2340d others(12): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912710
|
CTTTTTTT others(4): Show |
C | 39 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(36): Show | 39 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.674+2330_674+2340d others(13): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912710
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0232a0001c0001t0001g0249a0001c0001t0001g0250 | 3 | NA19056.hp1 NA19079.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.674+2329_674+2340d others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912710
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0001g0208a0001c0001t0001g0302 | 2 | HG01993.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.674+2327_674+2340d others(16): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912710
|
CTTTTTTT others(8): Show |
C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.674+2326_674+2340d others(17): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912710
|
CTTTTTTT others(11): Show |
C | 3 | a0001c0001t0001g0074a0001c0001t0001g0154a0001c0001t0001g0209 | 3 | HG02622.hp2 HG02895.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.674+2323_674+2340d others(20): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912710
|
CTTTTTTT others(14): Show |
C | 1 | a0001c0002t0002g0041 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.674+2320_674+2340d others(23): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912710
|
CTTTTTTT others(15): Show |
C | 60 | a0001c0001t0001g0056a0001c0002t0001g0289a0001c0002t0002g0008others(57): Show | 60 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.674+2319_674+2340d others(24): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77912710 | |||||
| chr7:77912749
|
T | G | 1 | a0001c0001t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.674+2340T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77912749 | ||||||
| chr7:77912902
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.674+2493G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77912902 | ||||||
| chr7:77912934
|
T | A | 1 | a0001c0001t0003g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.674+2525T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77912934 | ||||||
| chr7:77913249
|
G | A | 15 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(12): Show | 15 | HG01192.hp1 HG01243.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.674+2840G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77913249 | ||||||
| chr7:77913261
|
G | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0297 | 2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.674+2852G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77913261 | ||||||
| chr7:77913387
|
G | GA | 9 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(6): Show | 9 | HG00280.hp1 HG02451.hp1 HG04228.hp1 others(6): Show |
intron_variant | MODIFIER | c.674+2995dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77913387 | |||||
| chr7:77913387
|
GA | G | 8 | a0001c0001t0001g0092a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG00280.hp2 HG00323.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.674+2995delA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77913387 | |||||
| chr7:77913387
|
GAA | G | 15 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(12): Show | 15 | HG01192.hp1 HG01243.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.674+2994_674+2995d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77913387 | |||||
| chr7:77913388
|
A | G | 3 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071 | 3 | HG02257.hp2 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.674+2979A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77913388 | ||||||
| chr7:77913474
|
A | G | 22 | a0001c0001t0001g0018a0001c0001t0001g0084a0001c0001t0001g0088others(19): Show | 22 | HG00642.hp2 HG00735.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.674+3065A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77913474 | ||||||
| chr7:77913614
|
C | T | 1 | a0001c0002t0002g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.674+3205C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77913614 | ||||||
| chr7:77913697
|
C | A | 59 | a0001c0001t0001g0056a0001c0002t0002g0008a0001c0002t0002g0009others(56): Show | 59 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.674+3288C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77913697 | ||||||
| chr7:77913733
|
G | A | 3 | a0001c0001t0001g0302a0001c0002t0001g0289a0001c0002t0016g0290 | 3 | HG02559.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.674+3324G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77913733 | ||||||
| chr7:77913744
|
C | A | 17 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.674+3335C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77913744 | ||||||
| chr7:77913839
|
A | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 5 | NA18954.hp1 NA18974.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.674+3430A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77913839 | ||||||
| chr7:77914026
|
A | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.674+3617A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77914026 | ||||||
| chr7:77914055
|
G | A | 1 | a0001c0001t0005g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.674+3646G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77914055 | ||||||
| chr7:77914065
|
CA | C | 60 | a0001c0001t0001g0056a0001c0001t0001g0111a0001c0002t0002g0008others(57): Show | 60 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.674+3672delA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77914065 | |||||
| chr7:77914081
|
A | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.674+3672A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77914081 | ||||||
| chr7:77914113
|
A | G | 3 | a0001c0004t0007g0017a0001c0004t0007g0069a0001c0004t0007g0277 | 3 | HG02572.hp1 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.674+3704A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77914113 | ||||||
| chr7:77914194
|
C | T | 1 | a0001c0001t0005g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.674+3785C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77914194 | ||||||
| chr7:77914320
|
CAAG | C | 20 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(17): Show | 20 | HG00280.hp2 HG00323.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.674+3912_674+3914d others(5): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77914320 | ||||||
| chr7:77914335
|
G | T | 7 | a0001c0001t0001g0122a0001c0001t0001g0128a0001c0001t0001g0137others(4): Show | 7 | HG00621.hp2 HG01952.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.674+3926G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77914335 | ||||||
| chr7:77914340
|
A | G | 313 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.674+3931A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77914340 | ||||||
| chr7:77914426
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.674+4017C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77914426 | ||||||
| chr7:77914453
|
C | T | 1 | a0001c0002t0002g0288 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.674+4044C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77914453 | ||||||
| chr7:77914575
|
A | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.674+4166A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77914575 | ||||||
| chr7:77914702
|
T | G | 98 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.674+4293T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77914702 | ||||||
| chr7:77914883
|
G | T | 2 | a0001c0001t0001g0281a0001c0001t0001g0283 | 2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.674+4474G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77914883 | ||||||
| chr7:77914922
|
T | G | 5 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071others(2): Show | 5 | HG02257.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.674+4513T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77914922 | ||||||
| chr7:77915011
|
A | G | 3 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071 | 3 | HG02257.hp2 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.674+4602A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77915011 | ||||||
| chr7:77915100
|
T | TG | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.674+4695dupG | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77915100 | |||||
| chr7:77915170
|
A | C | 1 | a0001c0001t0001g0099 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.674+4761A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77915170 | ||||||
| chr7:77915297
|
C | T | 3 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071 | 3 | HG02257.hp2 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.674+4888C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77915297 | ||||||
| chr7:77915411
|
C | A | 1 | a0001c0002t0022g0080 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.675-4868C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77915411 | ||||||
| chr7:77915587
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.675-4692A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77915587 | ||||||
| chr7:77915674
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.675-4605G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77915674 | ||||||
| chr7:77915690
|
C | T | 1 | a0001c0002t0002g0055 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.675-4589C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77915690 | ||||||
| chr7:77915759
|
T | C | 74 | a0001c0001t0001g0302a0001c0001t0003g0306a0001c0001t0003g0307others(71): Show | 74 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.675-4520T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77915759 | ||||||
| chr7:77915787
|
T | A | 100 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.675-4492T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77915787 | ||||||
| chr7:77915811
|
G | A | 10 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.675-4468G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77915811 | ||||||
| chr7:77915859
|
T | C | 7 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(4): Show | 7 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.675-4420T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77915859 | ||||||
| chr7:77915902
|
A | C | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01169.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.675-4377A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77915902 | ||||||
| chr7:77915918
|
G | C | 3 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071 | 3 | HG02257.hp2 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.675-4361G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77915918 | ||||||
| chr7:77915946
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.675-4333G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77915946 | ||||||
| chr7:77915973
|
G | A | 1 | a0001c0001t0023g0278 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.675-4306G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77915973 | ||||||
| chr7:77915979
|
C | CTG | 44 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0082others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.675-4270_675-4269d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77915979 | |||||
| chr7:77915979
|
C | CTGTG | 84 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0074others(81): Show | 84 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.675-4272_675-4269d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77915979 | |||||
| chr7:77915979
|
C | CTGTGTG | 15 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0104others(12): Show | 15 | HG00099.hp2 HG01109.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.675-4274_675-4269d others(8): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77915979 | |||||
| chr7:77915979
|
C | CTGTGTGT others(3): Show |
1 | a0001c0001t0001g0123 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.675-4278_675-4269d others(12): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77915979 | |||||
| chr7:77915979
|
CTG | C | 22 | a0001c0001t0001g0184a0001c0001t0001g0188a0001c0001t0001g0291others(19): Show | 22 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.675-4270_675-4269d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77915979 | |||||
| chr7:77915979
|
CTGTG | C | 4 | a0001c0001t0001g0219a0001c0001t0001g0301a0001c0001t0005g0085others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.675-4272_675-4269d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77915979 | |||||
| chr7:77916209
|
A | C | 98 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.675-4070A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77916209 | ||||||
| chr7:77916231
|
A | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.675-4048A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77916231 | ||||||
| chr7:77916278
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.675-4001A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77916278 | ||||||
| chr7:77916424
|
T | G | 39 | a0001c0002t0002g0021a0001c0002t0002g0022a0001c0002t0002g0028others(36): Show | 39 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.675-3855T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77916424 | ||||||
| chr7:77916581
|
C | T | 1 | a0001c0002t0002g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.675-3698C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77916581 | ||||||
| chr7:77916875
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.675-3404C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77916875 | ||||||
| chr7:77916920
|
A | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.675-3359A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77916920 | ||||||
| chr7:77917449
|
A | G | 54 | a0001c0001t0001g0056a0001c0002t0002g0008a0001c0002t0002g0009others(51): Show | 54 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.675-2830A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77917449 | ||||||
| chr7:77917552
|
T | C | 3 | a0001c0001t0001g0014a0001c0002t0002g0065a0001c0002t0002g0068 | 3 | HG03942.hp2 HG04228.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.675-2727T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77917552 | ||||||
| chr7:77917636
|
A | G | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.675-2643A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77917636 | ||||||
| chr7:77917756
|
C | T | 78 | a0001c0001t0001g0056a0001c0001t0001g0302a0001c0001t0003g0306others(75): Show | 78 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.675-2523C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77917756 | ||||||
| chr7:77917764
|
C | G | 78 | a0001c0001t0001g0056a0001c0001t0001g0302a0001c0001t0003g0306others(75): Show | 78 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.675-2515C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77917764 | ||||||
| chr7:77917795
|
A | G | 12 | a0001c0001t0001g0056a0001c0002t0002g0022a0001c0002t0002g0028others(9): Show | 12 | HG02074.hp1 HG02129.hp1 NA18953.hp2 others(9): Show |
intron_variant | MODIFIER | c.675-2484A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77917795 | ||||||
| chr7:77917881
|
T | C | 178 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(175): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.675-2398T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77917881 | ||||||
| chr7:77918014
|
A | G | 1 | a0001c0001t0001g0007 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.675-2265A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77918014 | ||||||
| chr7:77918139
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.675-2140C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77918139 | ||||||
| chr7:77918197
|
T | C | 45 | a0001c0001t0001g0056a0001c0002t0002g0021a0001c0002t0002g0022others(42): Show | 45 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.675-2082T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77918197 | ||||||
| chr7:77918352
|
C | T | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.675-1927C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77918352 | ||||||
| chr7:77918551
|
C | T | 30 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(27): Show | 30 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.675-1728C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77918551 | ||||||
| chr7:77918582
|
A | T | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.675-1697A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77918582 | ||||||
| chr7:77918687
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.675-1592C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77918687 | ||||||
| chr7:77919029
|
A | G | 54 | a0001c0001t0001g0056a0001c0002t0002g0008a0001c0002t0002g0009others(51): Show | 54 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.675-1250A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77919029 | ||||||
| chr7:77919128
|
T | TA | 3 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071 | 3 | HG02257.hp2 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.675-1149dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr7 | 77919128 | |||||
| chr7:77919249
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.675-1030A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77919249 | ||||||
| chr7:77919296
|
G | A | 1 | a0001c0001t0009g0177 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.675-983G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77919296 | ||||||
| chr7:77919308
|
A | T | 1 | a0001c0001t0005g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.675-971A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77919308 | ||||||
| chr7:77919318
|
T | C | 12 | a0001c0001t0001g0056a0001c0002t0002g0022a0001c0002t0002g0028others(9): Show | 12 | HG02074.hp1 HG02129.hp1 NA18953.hp2 others(9): Show |
intron_variant | MODIFIER | c.675-961T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77919318 | ||||||
| chr7:77919818
|
G | A | 75 | a0001c0001t0001g0056a0001c0001t0001g0302a0001c0001t0003g0306others(72): Show | 75 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.675-461G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77919818 | ||||||
| chr7:77919928
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.675-351C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77919928 | ||||||
| chr7:77920004
|
C | A | 100 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.675-275C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77920004 | ||||||
| chr7:77920257
|
T | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.675-22T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 8/18 | chr7 | 77920257 | ||||||
| chr7:77920589
|
T | G | 61 | a0001c0001t0001g0056a0001c0002t0001g0289a0001c0002t0002g0008others(58): Show | 61 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.861+124T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | chr7 | 77920589 | ||||||
| chr7:77920705
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.861+240G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | chr7 | 77920705 | ||||||
| chr7:77920741
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.861+276G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | chr7 | 77920741 | ||||||
| chr7:77920796
|
C | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01109.hp2 HG01433.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.861+331C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | chr7 | 77920796 | ||||||
| chr7:77920845
|
C | T | 2 | a0001c0002t0013g0294a0001c0002t0020g0293 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.861+380C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | chr7 | 77920845 | ||||||
| chr7:77920895
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.861+430C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | chr7 | 77920895 | ||||||
| chr7:77920931
|
C | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG02027.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.861+466C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | chr7 | 77920931 | ||||||
| chr7:77921546
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.862-1077T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | chr7 | 77921546 | ||||||
| chr7:77921589
|
G | T | 1 | a0001c0001t0001g0243 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.862-1034G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | chr7 | 77921589 | ||||||
| chr7:77921750
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.862-873A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | chr7 | 77921750 | ||||||
| chr7:77921793
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.862-830C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | chr7 | 77921793 | ||||||
| chr7:77922017
|
C | CT | 20 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0030others(17): Show | 20 | HG00099.hp2 HG01433.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.862-583dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 77922017 | |||||
| chr7:77922017
|
C | CTT | 8 | a0001c0001t0001g0024a0001c0001t0001g0279a0001c0001t0001g0280others(5): Show | 8 | HG01884.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.862-584_862-583dup others(2): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 77922017 | |||||
| chr7:77922017
|
CT | C | 37 | a0001c0001t0001g0018a0001c0001t0001g0075a0001c0001t0001g0076others(34): Show | 37 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.862-583delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 77922017 | |||||
| chr7:77922017
|
CTT | C | 55 | a0001c0001t0001g0131a0001c0002t0001g0289a0001c0002t0002g0021others(52): Show | 55 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.862-584_862-583del others(2): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr7 | 77922017 | |||||
| chr7:77922071
|
A | G | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.862-552A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | chr7 | 77922071 | ||||||
| chr7:77922165
|
G | T | 100 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.862-458G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | chr7 | 77922165 | ||||||
| chr7:77922476
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.862-147G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 9/18 | chr7 | 77922476 | ||||||
| chr7:77922810
|
G | A | 174 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(171): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1017+32G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77922810 | ||||||
| chr7:77922917
|
A | G | 5 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0237others(2): Show | 5 | HG01943.hp1 HG01952.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+139A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77922917 | ||||||
| chr7:77922944
|
C | T | 7 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(4): Show | 7 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.1017+166C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77922944 | ||||||
| chr7:77923561
|
T | A | 4 | a0001c0002t0001g0289a0001c0002t0013g0294a0001c0002t0016g0290others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017+783T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77923561 | ||||||
| chr7:77923761
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1017+983C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77923761 | ||||||
| chr7:77923835
|
G | A | 1 | a0001c0001t0008g0145 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1017+1057G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77923835 | ||||||
| chr7:77924037
|
G | A | 53 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(50): Show | 53 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.1017+1259G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77924037 | ||||||
| chr7:77924100
|
T | C | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1017+1322T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77924100 | ||||||
| chr7:77924677
|
C | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0198 | 2 | NA18990.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1017+1899C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77924677 | ||||||
| chr7:77924845
|
G | A | 77 | a0001c0001t0001g0302a0001c0001t0003g0306a0001c0001t0003g0307others(74): Show | 77 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1017+2067G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77924845 | ||||||
| chr7:77924848
|
T | C | 77 | a0001c0001t0001g0302a0001c0001t0003g0306a0001c0001t0003g0307others(74): Show | 77 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1017+2070T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77924848 | ||||||
| chr7:77924977
|
C | T | 2 | a0001c0001t0005g0085a0001c0001t0005g0304 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1017+2199C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77924977 | ||||||
| chr7:77925097
|
C | T | 234 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(231): Show | 234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.1017+2319C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77925097 | ||||||
| chr7:77925160
|
A | T | 234 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(231): Show | 234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.1017+2382A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77925160 | ||||||
| chr7:77925257
|
A | G | 11 | a0001c0001t0001g0016a0001c0001t0001g0138a0001c0001t0001g0141others(8): Show | 11 | HG00423.hp2 HG00438.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1017+2479A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77925257 | ||||||
| chr7:77925280
|
T | A | 1 | a0004c0007t0001g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1017+2502T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77925280 | ||||||
| chr7:77925305
|
G | A | 99 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0074others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1017+2527G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77925305 | ||||||
| chr7:77925313
|
A | G | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | NA18946.hp1 NA18980.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1017+2535A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77925313 | ||||||
| chr7:77925319
|
C | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1017+2541C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77925319 | ||||||
| chr7:77925423
|
C | A | 1 | a0001c0001t0005g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1017+2645C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77925423 | ||||||
| chr7:77925487
|
T | G | 1 | a0001c0001t0001g0020 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1017+2709T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77925487 | ||||||
| chr7:77925495
|
G | GT | 23 | a0001c0001t0001g0012a0001c0001t0001g0186a0001c0001t0001g0219others(20): Show | 23 | HG00438.hp2 HG01258.hp1 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.1017+2748dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0001g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1017+2739_1017+274 others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
G | GTTTTTTT others(4): Show |
3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0187 | 3 | HG02486.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1017+2738_1017+274 others(15): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
G | GTTTTTTT others(5): Show |
2 | a0001c0001t0001g0184a0001c0001t0001g0188 | 2 | HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1017+2737_1017+274 others(16): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
G | GTTTTTTT others(7): Show |
1 | a0001c0001t0001g0291 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1017+2735_1017+274 others(18): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
G | GTTTTTTT others(8): Show |
1 | a0001c0001t0001g0292 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1017+2734_1017+274 others(19): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
G | GTTTTTTT others(9): Show |
1 | a0001c0001t0001g0212 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1017+2733_1017+274 others(20): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
G | GTTTTTTT others(10): Show |
2 | a0001c0001t0001g0183a0001c0001t0001g0185 | 2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1017+2732_1017+274 others(21): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
G | GTTTTTTT others(11): Show |
1 | a0001c0001t0001g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1017+2731_1017+274 others(22): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
G | GTTTTTTT others(13): Show |
1 | a0001c0001t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1017+2729_1017+274 others(24): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
GT | G | 33 | a0001c0001t0001g0056a0001c0001t0001g0078a0001c0001t0001g0101others(30): Show | 33 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1017+2748delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
GTT | G | 66 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0074others(63): Show | 66 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1017+2747_1017+274 others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
GTTT | G | 11 | a0001c0001t0001g0084a0001c0001t0001g0091a0001c0001t0001g0096others(8): Show | 11 | HG00735.hp1 HG01070.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.1017+2746_1017+274 others(7): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
GTTTT | G | 30 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(27): Show | 30 | HG00280.hp1 HG00642.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.1017+2745_1017+274 others(8): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
GTTTTTT | G | 6 | a0001c0001t0001g0302a0001c0002t0001g0289a0001c0002t0013g0294others(3): Show | 6 | HG01099.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1017+2743_1017+274 others(10): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
GTTTTTTT | G | 9 | a0001c0002t0002g0022a0001c0002t0002g0029a0001c0002t0002g0048others(6): Show | 9 | HG00733.hp1 HG02135.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1017+2742_1017+274 others(11): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
GTTTTTTT others(1): Show |
G | 47 | a0001c0001t0003g0306a0001c0002t0002g0008a0001c0002t0002g0009others(44): Show | 47 | HG00639.hp1 HG00741.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.1017+2741_1017+274 others(12): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
GTTTTTTT others(2): Show |
G | 7 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1017+2740_1017+274 others(13): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
GTTTTTTT others(3): Show |
G | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01109.hp2 HG01433.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1017+2739_1017+274 others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0001g0192 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1017+2737_1017+274 others(16): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925495
|
GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0001g0127 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1017+2736_1017+274 others(17): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77925495 | |||||
| chr7:77925688
|
G | C | 244 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(241): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1017+2910G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77925688 | ||||||
| chr7:77925727
|
G | A | 50 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1017+2949G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77925727 | ||||||
| chr7:77925848
|
G | A | 3 | a0001c0001t0001g0078a0001c0001t0001g0112a0001c0001t0001g0213 | 3 | HG00735.hp2 HG01255.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1017+3070G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77925848 | ||||||
| chr7:77925871
|
C | T | 43 | a0001c0002t0002g0021a0001c0002t0002g0022a0001c0002t0002g0028others(40): Show | 43 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1017+3093C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77925871 | ||||||
| chr7:77925874
|
G | A | 1 | a0001c0001t0014g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1017+3096G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77925874 | ||||||
| chr7:77926012
|
C | T | 2 | a0001c0002t0013g0294a0001c0002t0020g0293 | 2 | HG01099.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1018-3097C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77926012 | ||||||
| chr7:77926063
|
A | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0209 | 2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1018-3046A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77926063 | ||||||
| chr7:77926176
|
C | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1018-2933C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77926176 | ||||||
| chr7:77926224
|
C | G | 100 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1018-2885C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77926224 | ||||||
| chr7:77926237
|
A | G | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1018-2872A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77926237 | ||||||
| chr7:77926331
|
G | A | 3 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071 | 3 | HG02257.hp2 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1018-2778G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77926331 | ||||||
| chr7:77926377
|
G | C | 78 | a0001c0001t0001g0056a0001c0001t0001g0302a0001c0001t0003g0306others(75): Show | 78 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.1018-2732G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77926377 | ||||||
| chr7:77926582
|
C | CA | 14 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(11): Show | 14 | HG01884.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1018-2515dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77926582 | |||||
| chr7:77926704
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0209 | 2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1018-2405C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77926704 | ||||||
| chr7:77926849
|
C | T | 1 | a0001c0002t0002g0036 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1018-2260C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77926849 | ||||||
| chr7:77926883
|
G | A | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1018-2226G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77926883 | ||||||
| chr7:77926896
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1018-2213C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77926896 | ||||||
| chr7:77926910
|
C | A | 1 | a0001c0001t0001g0214 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1018-2199C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77926910 | ||||||
| chr7:77927118
|
GCTGCACT others(433): Show |
G | 1 | a0001c0001t0001g0120 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1018-1973_1018-153 others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927118 | |||||
| chr7:77927157
|
C | CAAA | 73 | a0001c0001t0001g0016a0001c0001t0001g0056a0001c0001t0001g0075others(70): Show | 73 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.1018-1933_1018-193 others(7): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927157 | |||||
| chr7:77927157
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1018-1945_1018-193 others(19): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927157 | |||||
| chr7:77927157
|
CA | C | 12 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(9): Show | 12 | HG01433.hp1 HG01517.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1018-1931delA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927157 | |||||
| chr7:77927157
|
CAA | C | 22 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0087others(19): Show | 22 | HG00280.hp1 HG01884.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1018-1932_1018-193 others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927157 | |||||
| chr7:77927171
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0002t0002g0033 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1018-1936_1018-192 others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927171 | |||||
| chr7:77927172
|
AAAAAAAT others(2): Show |
A | 48 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(45): Show | 48 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.1018-1935_1018-192 others(13): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927172 | |||||
| chr7:77927172
|
AAAAAAAT others(6): Show |
A | 4 | a0001c0002t0002g0049a0001c0002t0002g0050a0001c0002t0002g0059others(1): Show | 4 | HG03491.hp2 HG03492.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1018-1935_1018-192 others(17): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927172 | |||||
| chr7:77927173
|
A | T | 1 | a0001c0001t0005g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1018-1936A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927173 | ||||||
| chr7:77927175
|
A | T | 4 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0005g0085others(1): Show | 4 | HG02717.hp2 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1018-1934A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927175 | ||||||
| chr7:77927177
|
A | AAAAAAAA others(12): Show |
1 | a0001c0003t0004g0003 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1018-1931_1018-193 others(23): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927177 | |||||
| chr7:77927177
|
A | AAAAAAAA others(12): Show |
3 | a0001c0003t0004g0002a0001c0003t0004g0005a0001c0003t0004g0006 | 3 | HG01256.hp1 HG03239.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1018-1931_1018-193 others(23): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927177 | |||||
| chr7:77927177
|
A | AAAAAAAA others(14): Show |
1 | a0001c0003t0004g0004 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1018-1931_1018-193 others(25): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927177 | |||||
| chr7:77927177
|
A | AAAAAT | 8 | a0001c0001t0001g0074a0001c0001t0001g0105a0001c0001t0001g0106others(5): Show | 8 | HG00099.hp2 HG01109.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1018-1931_1018-193 others(9): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927177 | |||||
| chr7:77927177
|
A | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0261a0001c0001t0001g0297others(9): Show | 12 | HG01109.hp2 HG01517.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1018-1932A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927177 | ||||||
| chr7:77927177
|
AAT | A | 81 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0081others(78): Show | 81 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1018-1914_1018-191 others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927177 | |||||
| chr7:77927178
|
AT | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0117a0001c0001t0001g0152others(2): Show | 5 | HG00438.hp2 HG02738.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.1018-1930delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927178 | ||||||
| chr7:77927179
|
T | A | 5 | a0001c0001t0001g0302a0001c0001t0010g0072a0001c0001t0010g0073others(2): Show | 5 | HG02257.hp2 HG02258.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1018-1930T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927179 | ||||||
| chr7:77927181
|
T | A | 17 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(14): Show | 17 | HG00642.hp2 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1018-1928T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927181 | ||||||
| chr7:77927184
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1018-1925A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927184 | ||||||
| chr7:77927193
|
T | TACACACA others(3): Show |
6 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(3): Show | 6 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-1915_1018-191 others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927193 | |||||
| chr7:77927195
|
T | C | 12 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0259others(9): Show | 12 | HG01891.hp2 HG02055.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1018-1914T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927195 | ||||||
| chr7:77927195
|
T | TACACACA others(3): Show |
1 | a0001c0001t0003g0311 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1018-1911_1018-191 others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927195 | |||||
| chr7:77927195
|
TACATAC | T | 56 | a0001c0002t0001g0289a0001c0002t0002g0008a0001c0002t0002g0009others(53): Show | 56 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.1018-1910_1018-190 others(10): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927195 | |||||
| chr7:77927195
|
TACATACA others(7): Show |
T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1018-1910_1018-189 others(18): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927195 | |||||
| chr7:77927197
|
C | T | 21 | a0001c0001t0001g0117a0001c0001t0001g0152a0001c0001t0001g0225others(18): Show | 21 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.1018-1912C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927197 | ||||||
| chr7:77927199
|
T | C | 13 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0259others(10): Show | 13 | HG01891.hp2 HG02055.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.1018-1910T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927199 | ||||||
| chr7:77927199
|
T | TAC | 96 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1018-1886_1018-188 others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927199 | |||||
| chr7:77927201
|
C | T | 3 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071 | 3 | HG02257.hp2 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1018-1908C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927201 | ||||||
| chr7:77927203
|
C | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0152 | 2 | HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1018-1906C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927203 | ||||||
| chr7:77927211
|
CACACACA others(7): Show |
C | 6 | a0001c0001t0001g0224a0001c0001t0001g0228a0001c0001t0001g0229others(3): Show | 6 | HG00099.hp1 HG00741.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-1888_1018-187 others(18): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77927211 | |||||
| chr7:77927305
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1018-1804C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927305 | ||||||
| chr7:77927314
|
G | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(2): Show | 5 | HG01109.hp2 HG01433.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1018-1795G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927314 | ||||||
| chr7:77927550
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1018-1559C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927550 | ||||||
| chr7:77927632
|
G | A | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1018-1477G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927632 | ||||||
| chr7:77927697
|
T | G | 64 | a0001c0001t0001g0056a0001c0001t0010g0072a0001c0001t0010g0073others(61): Show | 64 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.1018-1412T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927697 | ||||||
| chr7:77927729
|
A | C | 10 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1018-1380A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927729 | ||||||
| chr7:77927811
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1018-1298A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77927811 | ||||||
| chr7:77928107
|
G | A | 4 | a0001c0002t0001g0289a0001c0002t0013g0294a0001c0002t0016g0290others(1): Show | 4 | HG01099.hp1 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1018-1002G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77928107 | ||||||
| chr7:77928186
|
C | CA | 23 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(20): Show | 23 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.1018-910dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77928186 | |||||
| chr7:77928216
|
A | G | 7 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(4): Show | 7 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.1018-893A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77928216 | ||||||
| chr7:77928351
|
T | A | 1 | a0004c0007t0001g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1018-758T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77928351 | ||||||
| chr7:77928357
|
T | G | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | NA19066.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1018-752T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77928357 | ||||||
| chr7:77928366
|
T | C | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1018-743T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77928366 | ||||||
| chr7:77928368
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1018-741T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77928368 | ||||||
| chr7:77928401
|
G | A | 244 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(241): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1018-708G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77928401 | ||||||
| chr7:77928486
|
T | TA | 56 | a0001c0001t0001g0056a0001c0001t0001g0291a0001c0001t0001g0292others(53): Show | 56 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.1018-612dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 77928486 | |||||
| chr7:77928503
|
G | A | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1018-606G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77928503 | ||||||
| chr7:77928537
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1018-572G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77928537 | ||||||
| chr7:77928704
|
A | T | 64 | a0001c0001t0001g0056a0001c0001t0010g0072a0001c0001t0010g0073others(61): Show | 64 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.1018-405A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77928704 | ||||||
| chr7:77928778
|
C | T | 50 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1018-331C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77928778 | ||||||
| chr7:77928923
|
T | G | 61 | a0001c0001t0001g0056a0001c0002t0001g0289a0001c0002t0002g0008others(58): Show | 61 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.1018-186T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77928923 | ||||||
| chr7:77929029
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1018-80A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77929029 | ||||||
| chr7:77929096
|
A | G | 3 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071 | 3 | HG02257.hp2 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1018-13A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 10/18 | chr7 | 77929096 | ||||||
| chr7:77929947
|
A | AT | 67 | a0001c0001t0001g0078a0001c0001t0001g0138a0001c0001t0001g0141others(64): Show | 67 | HG00423.hp2 HG00438.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.1236+641dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77929947 | |||||
| chr7:77929947
|
A | ATT | 6 | a0001c0002t0001g0289a0001c0002t0002g0054a0001c0002t0013g0294others(3): Show | 6 | HG01099.hp1 HG02559.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1236+640_1236+641d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77929947 | |||||
| chr7:77929947
|
AT | A | 7 | a0001c0001t0001g0074a0001c0001t0001g0083a0001c0001t0001g0094others(4): Show | 7 | HG01169.hp1 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1236+641delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77929947 | |||||
| chr7:77930022
|
T | C | 17 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1236+695T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77930022 | ||||||
| chr7:77930056
|
C | T | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1236+729C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77930056 | ||||||
| chr7:77930346
|
C | G | 1 | a0001c0001t0001g0159 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1236+1019C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77930346 | ||||||
| chr7:77930475
|
T | TC | 249 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(246): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.1236+1152dupC | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77930475 | |||||
| chr7:77930751
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1236+1424A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77930751 | ||||||
| chr7:77930918
|
A | T | 60 | a0001c0002t0001g0289a0001c0002t0002g0008a0001c0002t0002g0009others(57): Show | 60 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1236+1591A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77930918 | ||||||
| chr7:77931165
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1236+1838A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77931165 | ||||||
| chr7:77931179
|
A | G | 1 | a0001c0002t0002g0010 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1236+1852A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77931179 | ||||||
| chr7:77931313
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1236+1986C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77931313 | ||||||
| chr7:77931349
|
A | G | 46 | a0001c0001t0001g0056a0001c0001t0001g0261a0001c0002t0002g0021others(43): Show | 46 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.1236+2022A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77931349 | ||||||
| chr7:77931598
|
A | T | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0198 | 3 | HG02135.hp2 NA18990.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1236+2271A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77931598 | ||||||
| chr7:77931599
|
G | T | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0198 | 3 | HG02135.hp2 NA18990.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1236+2272G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77931599 | ||||||
| chr7:77931600
|
A | C | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0198 | 3 | HG02135.hp2 NA18990.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1236+2273A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77931600 | ||||||
| chr7:77931601
|
A | T | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0198 | 3 | HG02135.hp2 NA18990.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1236+2274A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77931601 | ||||||
| chr7:77931656
|
A | G | 61 | a0001c0001t0001g0056a0001c0002t0001g0289a0001c0002t0002g0008others(58): Show | 61 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.1236+2329A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77931656 | ||||||
| chr7:77931891
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1236+2564A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77931891 | ||||||
| chr7:77931960
|
C | T | 17 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1236+2633C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77931960 | ||||||
| chr7:77932057
|
C | T | 99 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0074others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1236+2730C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77932057 | ||||||
| chr7:77932079
|
C | T | 50 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1236+2752C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77932079 | ||||||
| chr7:77932493
|
C | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1236+3166C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77932493 | ||||||
| chr7:77932558
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1236+3231G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77932558 | ||||||
| chr7:77932585
|
GAAGAGAG others(9): Show |
G | 91 | a0001c0001t0001g0016a0001c0001t0001g0075a0001c0001t0001g0076others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1236+3275_1236+329 others(20): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932585 | |||||
| chr7:77932586
|
AAGAGAGA others(11): Show |
A | 3 | a0001c0001t0001g0074a0001c0001t0001g0121a0001c0001t0001g0172 | 3 | HG02293.hp2 HG02895.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1236+3275_1236+329 others(22): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932586 | |||||
| chr7:77932586
|
AAGAGAGA others(13): Show |
A | 2 | a0001c0001t0001g0020a0001c0001t0001g0103 | 2 | HG02896.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1236+3275_1236+329 others(24): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932586 | |||||
| chr7:77932588
|
GAGAGAGA others(7): Show |
G | 3 | a0001c0001t0001g0078a0001c0001t0001g0100a0001c0001t0001g0119 | 3 | HG02129.hp2 HG03942.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1236+3275_1236+328 others(18): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932588 | |||||
| chr7:77932598
|
G | A | 1 | a0001c0001t0017g0071 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1236+3271G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77932598 | ||||||
| chr7:77932602
|
A | AAG | 5 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1236+3294_1236+329 others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932602 | |||||
| chr7:77932615
|
AGAGAGAG others(7): Show |
A | 1 | a0001c0002t0002g0070 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1236+3290_1236+330 others(18): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932615 | |||||
| chr7:77932617
|
AGAGAGT | A | 6 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1236+3292_1236+329 others(10): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932617 | |||||
| chr7:77932617
|
AGAGAGTG others(3): Show |
A | 41 | a0001c0001t0001g0056a0001c0002t0002g0021a0001c0002t0002g0022others(38): Show | 41 | HG00733.hp1 HG01074.hp1 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.1236+3292_1236+330 others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932617 | |||||
| chr7:77932617
|
AGAGAGTG others(5): Show |
A | 11 | a0001c0002t0001g0289a0001c0002t0002g0039a0001c0002t0002g0043others(8): Show | 11 | HG00639.hp1 HG00741.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.1236+3292_1236+330 others(16): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932617 | |||||
| chr7:77932619
|
A | T | 5 | a0001c0001t0001g0078a0001c0001t0001g0100a0001c0001t0001g0119others(2): Show | 5 | HG02129.hp2 HG02630.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1236+3292A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77932619 | ||||||
| chr7:77932619
|
AGAGTGTG others(3): Show |
A | 1 | a0001c0002t0002g0215 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1236+3294_1236+330 others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932619 | |||||
| chr7:77932621
|
A | AGAGAGAG others(5): Show |
1 | a0001c0001t0001g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1236+3295_1236+329 others(16): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932621 | |||||
| chr7:77932621
|
A | AGAGT | 22 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(19): Show | 22 | HG00280.hp2 HG00323.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.1236+3295_1236+329 others(8): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932621 | |||||
| chr7:77932621
|
A | AGAGTGT | 3 | a0001c0001t0001g0191a0001c0001t0001g0198a0001c0001t0003g0310 | 3 | HG02055.hp2 HG02135.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1236+3295_1236+329 others(10): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932621 | |||||
| chr7:77932621
|
A | AGAGTGTG others(7): Show |
2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1236+3295_1236+329 others(18): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932621 | |||||
| chr7:77932621
|
A | AGT | 10 | a0001c0001t0001g0007a0001c0001t0001g0218a0001c0001t0001g0219others(7): Show | 10 | HG02004.hp2 HG02015.hp2 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.1236+3329_1236+333 others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932621 | |||||
| chr7:77932621
|
A | AGTGTGT | 5 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0291others(2): Show | 5 | HG01109.hp2 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1236+3325_1236+333 others(10): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932621 | |||||
| chr7:77932621
|
A | AGTGTGTG others(1): Show |
3 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0292 | 3 | HG00735.hp1 HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1236+3323_1236+333 others(12): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932621 | |||||
| chr7:77932621
|
A | AGTGTGTG others(3): Show |
17 | a0001c0001t0001g0019a0001c0001t0001g0084a0001c0001t0001g0086others(14): Show | 17 | HG00280.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1236+3321_1236+333 others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932621 | |||||
| chr7:77932621
|
A | AGTGTGTG others(5): Show |
3 | a0001c0001t0001g0018a0001c0001t0001g0200a0001c0001t0001g0221 | 3 | HG00642.hp2 HG02080.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1236+3319_1236+333 others(16): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932621 | |||||
| chr7:77932621
|
A | T | 99 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0024others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1236+3294A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77932621 | ||||||
| chr7:77932621
|
AGT | A | 7 | a0001c0001t0001g0267a0001c0001t0010g0073a0001c0003t0004g0002others(4): Show | 7 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1236+3329_1236+333 others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932621 | |||||
| chr7:77932621
|
AGTGTGT | A | 5 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0274others(2): Show | 5 | HG00639.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1236+3325_1236+333 others(10): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77932621 | |||||
| chr7:77932623
|
T | A | 12 | a0001c0001t0001g0020a0001c0001t0001g0103a0001c0001t0001g0244others(9): Show | 12 | HG01123.hp2 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1236+3296T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77932623 | ||||||
| chr7:77932629
|
T | A | 1 | a0001c0001t0003g0309 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1236+3302T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77932629 | ||||||
| chr7:77932763
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1236+3436A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77932763 | ||||||
| chr7:77932977
|
G | A | 170 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(167): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.1236+3650G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77932977 | ||||||
| chr7:77933054
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1236+3727C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77933054 | ||||||
| chr7:77933062
|
C | T | 4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(1): Show | 4 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1236+3735C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77933062 | ||||||
| chr7:77933110
|
T | C | 232 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(229): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.1236+3783T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77933110 | ||||||
| chr7:77933213
|
G | C | 1 | a0001c0001t0001g0271 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1236+3886G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77933213 | ||||||
| chr7:77933232
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG00280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1236+3905C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77933232 | ||||||
| chr7:77933284
|
A | G | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(2): Show | 5 | HG02027.hp2 HG02080.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1236+3957A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77933284 | ||||||
| chr7:77933372
|
A | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1236+4045A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77933372 | ||||||
| chr7:77933631
|
C | G | 4 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237-4079C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77933631 | ||||||
| chr7:77933710
|
TG | T | 24 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(21): Show | 24 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1237-3999delG | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77933710 | ||||||
| chr7:77933711
|
G | GT | 79 | a0001c0001t0001g0056a0001c0001t0001g0128a0001c0001t0001g0141others(76): Show | 79 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1237-3981dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77933711 | |||||
| chr7:77933711
|
G | T | 4 | a0001c0001t0001g0092a0001c0001t0001g0196a0001c0001t0001g0197others(1): Show | 4 | HG02055.hp1 HG02071.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237-3999G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77933711 | ||||||
| chr7:77933711
|
GT | G | 25 | a0001c0001t0001g0074a0001c0001t0001g0175a0001c0001t0001g0178others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.1237-3981delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77933711 | |||||
| chr7:77934105
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1237-3605A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77934105 | ||||||
| chr7:77934203
|
A | C | 4 | a0001c0002t0002g0033a0001c0002t0002g0034a0001c0002t0002g0035others(1): Show | 4 | HG02135.hp1 NA18747.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237-3507A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77934203 | ||||||
| chr7:77934326
|
C | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237-3384C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77934326 | ||||||
| chr7:77934362
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1237-3348A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77934362 | ||||||
| chr7:77934385
|
A | T | 61 | a0001c0001t0001g0056a0001c0002t0001g0289a0001c0002t0002g0008others(58): Show | 61 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.1237-3325A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77934385 | ||||||
| chr7:77934393
|
T | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237-3317T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77934393 | ||||||
| chr7:77934394
|
T | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237-3316T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77934394 | ||||||
| chr7:77934438
|
A | C | 3 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071 | 3 | HG02257.hp2 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1237-3272A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77934438 | ||||||
| chr7:77934500
|
A | T | 238 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(235): Show | 238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.1237-3210A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77934500 | ||||||
| chr7:77934627
|
A | C | 1 | a0001c0001t0009g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1237-3083A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77934627 | ||||||
| chr7:77934826
|
G | T | 2 | a0001c0002t0002g0049a0001c0002t0002g0050 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1237-2884G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77934826 | ||||||
| chr7:77934890
|
C | T | 5 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(2): Show | 5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237-2820C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77934890 | ||||||
| chr7:77934951
|
C | CA | 10 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(7): Show | 10 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1237-2748dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77934951 | |||||
| chr7:77934992
|
A | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1237-2718A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77934992 | ||||||
| chr7:77935038
|
T | C | 4 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG00639.hp2 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237-2672T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935038 | ||||||
| chr7:77935043
|
C | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1237-2667C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935043 | ||||||
| chr7:77935047
|
T | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0173 | 2 | NA18945.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1237-2663T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935047 | ||||||
| chr7:77935068
|
C | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1237-2642C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935068 | ||||||
| chr7:77935096
|
A | T | 1 | a0001c0001t0018g0160 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1237-2614A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935096 | ||||||
| chr7:77935112
|
G | T | 1 | a0001c0002t0002g0027 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1237-2598G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935112 | ||||||
| chr7:77935120
|
T | TC | 13 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(10): Show | 13 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1237-2580dupC | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77935120 | |||||
| chr7:77935121
|
C | T | 67 | a0001c0001t0001g0056a0001c0001t0001g0302a0001c0002t0001g0289others(64): Show | 67 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.1237-2589C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935121 | ||||||
| chr7:77935123
|
C | T | 8 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(5): Show | 8 | HG02055.hp2 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1237-2587C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935123 | ||||||
| chr7:77935126
|
C | G | 1 | a0001c0001t0019g0066 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1237-2584C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935126 | ||||||
| chr7:77935127
|
C | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030 | 3 | HG01433.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1237-2583C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935127 | ||||||
| chr7:77935129
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1237-2581C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935129 | ||||||
| chr7:77935129
|
C | G | 30 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(27): Show | 30 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1237-2581C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935129 | ||||||
| chr7:77935129
|
CCA | C | 162 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1237-2568_1237-256 others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77935129 | |||||
| chr7:77935130
|
CA | C | 46 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0023others(43): Show | 46 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1237-2579delA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935130 | ||||||
| chr7:77935131
|
A | C | 25 | a0001c0001t0001g0186a0001c0001t0001g0224a0001c0001t0001g0228others(22): Show | 25 | HG00099.hp1 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1237-2579A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935131 | ||||||
| chr7:77935133
|
A | C | 9 | a0001c0001t0001g0121a0001c0001t0001g0266a0001c0001t0001g0273others(6): Show | 9 | HG00639.hp2 HG02135.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.1237-2577A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935133 | ||||||
| chr7:77935214
|
C | CT | 90 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0056others(87): Show | 90 | HG00280.hp1 HG00642.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.1237-2470dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77935214 | |||||
| chr7:77935214
|
C | CTT | 19 | a0001c0001t0001g0191a0001c0001t0005g0304a0001c0002t0001g0289others(16): Show | 19 | HG00639.hp1 HG01099.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1237-2471_1237-247 others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77935214 | |||||
| chr7:77935214
|
CT | C | 84 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0074others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1237-2470delT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77935214 | |||||
| chr7:77935249
|
G | C | 3 | a0001c0002t0002g0031a0001c0002t0002g0048a0001c0002t0002g0058 | 3 | HG02970.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1237-2461G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935249 | ||||||
| chr7:77935286
|
G | A | 1 | a0001c0001t0001g0305 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1237-2424G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935286 | ||||||
| chr7:77935331
|
T | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1237-2379T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935331 | ||||||
| chr7:77935470
|
C | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1237-2240C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935470 | ||||||
| chr7:77935669
|
A | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1237-2041A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77935669 | ||||||
| chr7:77936242
|
C | T | 6 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1237-1468C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77936242 | ||||||
| chr7:77936356
|
C | T | 3 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0120 | 3 | HG01257.hp2 HG01943.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1237-1354C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77936356 | ||||||
| chr7:77936357
|
G | A | 1 | a0001c0001t0001g0262 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1237-1353G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77936357 | ||||||
| chr7:77936639
|
A | T | 1 | a0001c0004t0007g0017 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1237-1071A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77936639 | ||||||
| chr7:77936669
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1237-1041G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77936669 | ||||||
| chr7:77936706
|
T | TAAAAATA others(319): Show |
2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1237-988_1237-987i others(328): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77936706 | |||||
| chr7:77936706
|
T | TAAAAATA others(320): Show |
4 | a0001c0002t0013g0294a0001c0004t0007g0017a0001c0004t0007g0069others(1): Show | 4 | HG01099.hp1 HG02572.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237-988_1237-987i others(329): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77936706 | |||||
| chr7:77936706
|
T | TAAAAATA others(321): Show |
1 | a0001c0002t0020g0293 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1237-988_1237-987i others(330): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77936706 | |||||
| chr7:77936706
|
T | TAAAAATA others(320): Show |
1 | a0001c0002t0002g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1237-988_1237-987i others(329): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77936706 | |||||
| chr7:77936706
|
T | TAAAAATA others(311): Show |
12 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0002g0034others(9): Show | 12 | HG02135.hp1 HG03017.hp1 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.1237-988_1237-987i others(320): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77936706 | |||||
| chr7:77936706
|
T | TAAAAATA others(319): Show |
15 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(12): Show | 15 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1237-988_1237-987i others(328): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77936706 | |||||
| chr7:77936706
|
T | TAAAAATA others(320): Show |
23 | a0001c0002t0002g0021a0001c0002t0002g0022a0001c0002t0002g0028others(20): Show | 23 | HG00639.hp1 HG00741.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1237-988_1237-987i others(329): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77936706 | |||||
| chr7:77936706
|
T | TAAAAATA others(321): Show |
2 | a0001c0002t0002g0029a0001c0002t0002g0288 | 2 | HG03130.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1237-988_1237-987i others(330): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77936706 | |||||
| chr7:77936706
|
T | TAAAAATA others(320): Show |
2 | a0001c0001t0010g0072a0001c0001t0010g0073 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1237-988_1237-987i others(329): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77936706 | |||||
| chr7:77936706
|
T | TAAAAATA others(321): Show |
1 | a0001c0001t0017g0071 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1237-988_1237-987i others(330): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77936706 | |||||
| chr7:77936727
|
G | T | 1 | a0001c0001t0005g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1237-983G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77936727 | ||||||
| chr7:77936984
|
A | G | 12 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(9): Show | 12 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.1237-726A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77936984 | ||||||
| chr7:77937080
|
GA | G | 60 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(57): Show | 60 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1237-617delA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77937080 | |||||
| chr7:77937129
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1237-581A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77937129 | ||||||
| chr7:77937430
|
G | A | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1237-280G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77937430 | ||||||
| chr7:77937475
|
GCTAA | G | 7 | a0001c0001t0001g0122a0001c0001t0001g0128a0001c0001t0001g0137others(4): Show | 7 | HG00621.hp2 HG01952.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1237-230_1237-227d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77937475 | |||||
| chr7:77937674
|
G | A | 13 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(10): Show | 13 | HG01433.hp1 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1237-36G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | chr7 | 77937674 | ||||||
| chr7:77937691
|
A | AT | 11 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(8): Show | 11 | HG01109.hp2 HG02055.hp2 HG02630.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.1237-5dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr7 | 77937691 | |||||
| chr7:77937948
|
C | G | 52 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(49): Show | 52 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1365+110C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77937948 | ||||||
| chr7:77938183
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1365+345T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77938183 | ||||||
| chr7:77938456
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1365+618C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77938456 | ||||||
| chr7:77938461
|
T | C | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(1): Show | 4 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+623T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77938461 | ||||||
| chr7:77938546
|
T | C | 1 | a0004c0007t0001g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1365+708T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77938546 | ||||||
| chr7:77938557
|
C | CGTCTCTA others(40): Show |
1 | a0001c0001t0003g0307 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1365+743_1365+789d others(49): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr7 | 77938557 | |||||
| chr7:77938641
|
G | T | 1 | a0001c0001t0001g0056 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1365+803G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77938641 | ||||||
| chr7:77938669
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1365+831C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77938669 | ||||||
| chr7:77938696
|
T | G | 181 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.1365+858T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77938696 | ||||||
| chr7:77938746
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1365+908C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77938746 | ||||||
| chr7:77938755
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0297 | 2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1365+917C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77938755 | ||||||
| chr7:77938931
|
G | A | 1 | a0001c0002t0002g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1365+1093G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77938931 | ||||||
| chr7:77939000
|
G | C | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1366-1030G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77939000 | ||||||
| chr7:77939022
|
C | T | 1 | a0001c0001t0006g0296 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1366-1008C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77939022 | ||||||
| chr7:77939474
|
G | A | 13 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(10): Show | 13 | HG01433.hp1 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1366-556G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77939474 | ||||||
| chr7:77939475
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1366-555C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77939475 | ||||||
| chr7:77939482
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1366-548G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77939482 | ||||||
| chr7:77939544
|
T | C | 80 | a0001c0001t0001g0056a0001c0001t0001g0302a0001c0001t0003g0306others(77): Show | 80 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.1366-486T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77939544 | ||||||
| chr7:77939548
|
C | G | 66 | a0001c0001t0001g0056a0001c0001t0005g0025a0001c0001t0005g0026others(63): Show | 66 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.1366-482C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77939548 | ||||||
| chr7:77939589
|
C | CA | 15 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0127others(12): Show | 15 | HG00140.hp2 HG01099.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1366-422dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr7 | 77939589 | |||||
| chr7:77939589
|
C | CAA | 60 | a0001c0001t0001g0056a0001c0001t0005g0025a0001c0001t0005g0026others(57): Show | 60 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1366-423_1366-422d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr7 | 77939589 | |||||
| chr7:77939589
|
CA | C | 21 | a0001c0001t0001g0156a0001c0001t0001g0175a0001c0001t0001g0178others(18): Show | 21 | HG00280.hp2 HG00323.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1366-422delA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr7 | 77939589 | |||||
| chr7:77939647
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1366-383C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77939647 | ||||||
| chr7:77939718
|
T | C | 7 | a0001c0002t0001g0289a0001c0002t0013g0294a0001c0002t0016g0290others(4): Show | 7 | HG01099.hp1 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-312T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77939718 | ||||||
| chr7:77939827
|
C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0143 | 2 | NA19055.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1366-203C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 12/18 | chr7 | 77939827 | ||||||
| chr7:77940415
|
A | T | 30 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(27): Show | 30 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1638+113A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 13/18 | chr7 | 77940415 | ||||||
| chr7:77940470
|
A | T | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1639-58A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 13/18 | chr7 | 77940470 | ||||||
| chr7:77940879
|
C | A | 60 | a0001c0002t0001g0289a0001c0002t0002g0008a0001c0002t0002g0009others(57): Show | 60 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1770+220C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 14/18 | chr7 | 77940879 | ||||||
| chr7:77941441
|
A | G | 64 | a0001c0001t0001g0056a0001c0001t0010g0072a0001c0001t0010g0073others(61): Show | 64 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.1770+782A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 14/18 | chr7 | 77941441 | ||||||
| chr7:77941506
|
T | C | 4 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG00639.hp2 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1770+847T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 14/18 | chr7 | 77941506 | ||||||
| chr7:77941563
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1770+904G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 14/18 | chr7 | 77941563 | ||||||
| chr7:77941635
|
A | G | 3 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071 | 3 | HG02257.hp2 HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1770+976A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 14/18 | chr7 | 77941635 | ||||||
| chr7:77941647
|
T | C | 1 | a0001c0001t0005g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1770+988T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 14/18 | chr7 | 77941647 | ||||||
| chr7:77941693
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1771-1007C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 14/18 | chr7 | 77941693 | ||||||
| chr7:77942168
|
A | T | 1 | a0001c0001t0001g0207 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1771-532A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 14/18 | chr7 | 77942168 | ||||||
| chr7:77942182
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1771-518G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 14/18 | chr7 | 77942182 | ||||||
| chr7:77942203
|
A | G | 3 | a0001c0002t0002g0062a0001c0002t0002g0063a0001c0002t0002g0064 | 3 | NA18953.hp2 NA18960.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1771-497A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 14/18 | chr7 | 77942203 | ||||||
| chr7:77942336
|
G | A | 2 | a0001c0001t0005g0085a0001c0001t0005g0304 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1771-364G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 14/18 | chr7 | 77942336 | ||||||
| chr7:77942554
|
A | G | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1771-146A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 14/18 | chr7 | 77942554 | ||||||
| chr7:77943085
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0163 | 2 | HG01243.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1857+299A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77943085 | ||||||
| chr7:77943110
|
C | CT | 100 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1857+328dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77943110 | |||||
| chr7:77943111
|
T | TTTTC | 6 | a0001c0001t0001g0019a0001c0003t0004g0002a0001c0003t0004g0003others(3): Show | 6 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1857+345_1857+348d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77943111 | |||||
| chr7:77943144
|
T | C | 248 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(245): Show | 248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1857+358T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77943144 | ||||||
| chr7:77943173
|
T | G | 5 | a0001c0001t0001g0232a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | NA18980.hp1 NA19056.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.1857+387T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77943173 | ||||||
| chr7:77943207
|
G | T | 1 | a0001c0001t0001g0168 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1857+421G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77943207 | ||||||
| chr7:77943214
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1857+428G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77943214 | ||||||
| chr7:77943507
|
CTTAG | C | 100 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1857+726_1857+729d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77943507 | |||||
| chr7:77943815
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1857+1029C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77943815 | ||||||
| chr7:77943839
|
A | G | 248 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(245): Show | 248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1857+1053A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77943839 | ||||||
| chr7:77943843
|
C | T | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1857+1057C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77943843 | ||||||
| chr7:77944147
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1857+1361A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77944147 | ||||||
| chr7:77944406
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1857+1620C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77944406 | ||||||
| chr7:77944416
|
G | A | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1857+1630G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77944416 | ||||||
| chr7:77944549
|
C | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0209 | 2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1857+1763C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77944549 | ||||||
| chr7:77944685
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1857+1899C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77944685 | ||||||
| chr7:77944985
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0129a0001c0001t0001g0140 | 3 | HG03491.hp1 HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1857+2199G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77944985 | ||||||
| chr7:77945137
|
C | T | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1857+2351C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77945137 | ||||||
| chr7:77945140
|
A | G | 6 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(3): Show | 6 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1857+2354A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77945140 | ||||||
| chr7:77945202
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1857+2416G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77945202 | ||||||
| chr7:77945211
|
G | A | 1 | a0001c0002t0002g0022 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1857+2425G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77945211 | ||||||
| chr7:77945211
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1857+2425G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77945211 | ||||||
| chr7:77945216
|
T | C | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1857+2430T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77945216 | ||||||
| chr7:77945324
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1857+2538A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77945324 | ||||||
| chr7:77945462
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1857+2676A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77945462 | ||||||
| chr7:77945480
|
T | TAAAAACT others(312): Show |
4 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1857+2709_1857+271 others(323): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77945480 | |||||
| chr7:77945480
|
T | TAAAAACT others(313): Show |
1 | a0001c0003t0004g0003 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1857+2709_1857+271 others(324): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77945480 | |||||
| chr7:77945575
|
T | C | 1 | a0001c0002t0002g0288 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1857+2789T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77945575 | ||||||
| chr7:77945738
|
T | G | 1 | a0001c0002t0002g0070 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1857+2952T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77945738 | ||||||
| chr7:77945789
|
C | A | 1 | a0001c0001t0018g0160 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1857+3003C>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77945789 | ||||||
| chr7:77945848
|
A | C | 1 | a0001c0001t0001g0202 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1857+3062A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77945848 | ||||||
| chr7:77946121
|
T | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1857+3335T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77946121 | ||||||
| chr7:77946174
|
A | T | 1 | a0001c0001t0001g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1857+3388A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77946174 | ||||||
| chr7:77946187
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1857+3401A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77946187 | ||||||
| chr7:77946264
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1858-3414G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77946264 | ||||||
| chr7:77946384
|
T | C | 313 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1858-3294T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77946384 | ||||||
| chr7:77946493
|
T | C | 3 | a0001c0002t0002g0039a0001c0002t0002g0043a0001c0002t0002g0055 | 3 | HG00639.hp1 HG00741.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1858-3185T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77946493 | ||||||
| chr7:77946603
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1858-3075A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77946603 | ||||||
| chr7:77946629
|
C | T | 63 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071others(60): Show | 63 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.1858-3049C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77946629 | ||||||
| chr7:77946742
|
C | T | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1858-2936C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77946742 | ||||||
| chr7:77946847
|
G | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1858-2831G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77946847 | ||||||
| chr7:77946892
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1858-2786T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77946892 | ||||||
| chr7:77946958
|
C | CA | 10 | a0001c0001t0001g0127a0001c0001t0001g0191a0001c0001t0001g0201others(7): Show | 10 | HG00140.hp2 HG01109.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1858-2705dupA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77946958 | |||||
| chr7:77946958
|
C | CAA | 6 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(3): Show | 6 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1858-2706_1858-270 others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77946958 | |||||
| chr7:77947041
|
G | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1858-2637G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77947041 | ||||||
| chr7:77947125
|
A | AAACAACA others(2): Show |
74 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(71): Show | 74 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.1858-2547_1858-253 others(13): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77947125 | |||||
| chr7:77947141
|
C | T | 1 | a0001c0002t0022g0080 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1858-2537C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77947141 | ||||||
| chr7:77947161
|
G | GCAA | 66 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0017g0071others(63): Show | 66 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.1858-2498_1858-249 others(7): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77947161 | |||||
| chr7:77947269
|
G | A | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1858-2409G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77947269 | ||||||
| chr7:77947330
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1858-2348C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77947330 | ||||||
| chr7:77947331
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1858-2347G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77947331 | ||||||
| chr7:77947391
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1858-2287A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77947391 | ||||||
| chr7:77947420
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1858-2258C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77947420 | ||||||
| chr7:77947545
|
A | G | 1 | a0001c0001t0005g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1858-2133A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77947545 | ||||||
| chr7:77947621
|
G | A | 50 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1858-2057G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77947621 | ||||||
| chr7:77947668
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1858-2010C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77947668 | ||||||
| chr7:77947826
|
C | CTTTCTTT others(9): Show |
1 | a0001c0001t0003g0311 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1858-1849_1858-184 others(20): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77947826 | |||||
| chr7:77947826
|
C | CTTTCTTT others(10): Show |
1 | a0001c0001t0003g0306 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1858-1849_1858-184 others(21): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77947826 | |||||
| chr7:77947826
|
C | CTTTCTTT others(12): Show |
1 | a0001c0001t0003g0310 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1858-1849_1858-184 others(23): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77947826 | |||||
| chr7:77947826
|
C | CTTTCTTT others(13): Show |
1 | a0001c0001t0003g0309 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1858-1849_1858-184 others(24): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77947826 | |||||
| chr7:77947827
|
TTTTTTCT others(3): Show |
T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1858-1845_1858-183 others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77947827 | |||||
| chr7:77947830
|
T | C | 3 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0021g0312 | 3 | HG02717.hp2 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1858-1848T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77947830 | ||||||
| chr7:77947833
|
C | T | 4 | a0001c0001t0003g0306a0001c0001t0003g0309a0001c0001t0003g0310others(1): Show | 4 | HG02055.hp2 HG02976.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1858-1845C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77947833 | ||||||
| chr7:77947837
|
C | CT | 9 | a0001c0001t0001g0015a0001c0001t0001g0267a0001c0001t0001g0299others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1858-1823dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77947837 | |||||
| chr7:77947837
|
C | CTTTTTT | 50 | a0001c0001t0005g0304a0001c0002t0002g0008a0001c0002t0002g0009others(47): Show | 50 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.1858-1828_1858-182 others(10): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77947837 | |||||
| chr7:77947837
|
C | CTTTTTTT | 6 | a0001c0002t0002g0040a0001c0002t0002g0044a0001c0002t0002g0053others(3): Show | 6 | HG02970.hp1 HG04115.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.1858-1829_1858-182 others(11): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77947837 | |||||
| chr7:77947837
|
C | CTTTTTTT others(3): Show |
7 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0279others(4): Show | 7 | HG01433.hp1 HG01884.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1858-1832_1858-182 others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77947837 | |||||
| chr7:77947837
|
C | CTTTTTTT others(4): Show |
68 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0024others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.1858-1833_1858-182 others(15): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77947837 | |||||
| chr7:77947837
|
C | CTTTTTTT others(5): Show |
57 | a0001c0001t0001g0076a0001c0001t0001g0078a0001c0001t0001g0081others(54): Show | 57 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1858-1834_1858-182 others(16): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77947837 | |||||
| chr7:77947837
|
C | CTTTTTTT others(6): Show |
26 | a0001c0001t0001g0018a0001c0001t0001g0091a0001c0001t0001g0093others(23): Show | 26 | HG00642.hp2 HG00735.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1858-1835_1858-182 others(17): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77947837 | |||||
| chr7:77947837
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0019a0001c0001t0001g0088 | 2 | HG01517.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1858-1836_1858-182 others(18): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77947837 | |||||
| chr7:77947837
|
C | CTTTTTTT others(8): Show |
4 | a0001c0003t0004g0002a0001c0003t0004g0004a0001c0003t0004g0005others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1858-1837_1858-182 others(19): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77947837 | |||||
| chr7:77947837
|
C | CTTTTTTT others(9): Show |
2 | a0001c0001t0005g0026a0001c0003t0004g0003 | 2 | HG00642.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1858-1838_1858-182 others(20): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77947837 | |||||
| chr7:77947837
|
C | T | 9 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0003g0306others(6): Show | 9 | HG01071.hp1 HG01074.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1858-1841C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77947837 | ||||||
| chr7:77947840
|
T | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1858-1838T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77947840 | ||||||
| chr7:77947877
|
C | T | 58 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(55): Show | 58 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.1858-1801C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77947877 | ||||||
| chr7:77947907
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1858-1771C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77947907 | ||||||
| chr7:77948117
|
G | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1858-1561G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77948117 | ||||||
| chr7:77948241
|
A | T | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1858-1437A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77948241 | ||||||
| chr7:77948253
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1858-1425A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77948253 | ||||||
| chr7:77948263
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1858-1415A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77948263 | ||||||
| chr7:77948288
|
T | C | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1858-1390T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77948288 | ||||||
| chr7:77948368
|
T | C | 65 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0001t0010g0072others(62): Show | 65 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.1858-1310T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77948368 | ||||||
| chr7:77948401
|
A | G | 4 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG00639.hp2 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1858-1277A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77948401 | ||||||
| chr7:77948442
|
A | T | 60 | a0001c0001t0005g0025a0001c0001t0005g0026a0001c0002t0002g0008others(57): Show | 60 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1858-1236A>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77948442 | ||||||
| chr7:77948448
|
TA | T | 20 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(17): Show | 20 | HG00280.hp2 HG00323.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.1858-1228delA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77948448 | |||||
| chr7:77948452
|
A | G | 6 | a0001c0001t0001g0224a0001c0001t0001g0228a0001c0001t0001g0229others(3): Show | 6 | HG00099.hp1 HG00741.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1858-1226A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77948452 | ||||||
| chr7:77948501
|
A | C | 101 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(98): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1858-1177A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77948501 | ||||||
| chr7:77948588
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1858-1090A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77948588 | ||||||
| chr7:77948654
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1858-1024G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77948654 | ||||||
| chr7:77948679
|
T | C | 7 | a0001c0001t0001g0122a0001c0001t0001g0128a0001c0001t0001g0137others(4): Show | 7 | HG00621.hp2 HG01952.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1858-999T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77948679 | ||||||
| chr7:77948721
|
T | G | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1858-957T>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77948721 | ||||||
| chr7:77948727
|
A | G | 5 | a0001c0003t0004g0002a0001c0003t0004g0003a0001c0003t0004g0004others(2): Show | 5 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1858-951A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77948727 | ||||||
| chr7:77948827
|
G | C | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1858-851G>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77948827 | ||||||
| chr7:77949062
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1858-616A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77949062 | ||||||
| chr7:77949107
|
CAT | C | 58 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(55): Show | 58 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.1858-569_1858-568d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77949107 | |||||
| chr7:77949218
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1858-460C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77949218 | ||||||
| chr7:77949500
|
C | T | 1 | a0001c0001t0001g0313 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1858-178C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | chr7 | 77949500 | ||||||
| chr7:77949582
|
TA | T | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1858-94delA | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 77949582 | |||||
| chr7:77949914
|
G | A | 4 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG00642.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2013+81G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | chr7 | 77949914 | ||||||
| chr7:77950225
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2013+392C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | chr7 | 77950225 | ||||||
| chr7:77950379
|
C | T | 1 | a0001c0002t0002g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2013+546C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | chr7 | 77950379 | ||||||
| chr7:77950390
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2013+557G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | chr7 | 77950390 | ||||||
| chr7:77950451
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2013+618A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | chr7 | 77950451 | ||||||
| chr7:77950586
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0014g0150 | 2 | HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2013+753C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | chr7 | 77950586 | ||||||
| chr7:77950608
|
T | C | 1 | a0001c0002t0022g0080 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2013+775T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | chr7 | 77950608 | ||||||
| chr7:77950742
|
A | G | 2 | a0001c0001t0001g0302a0003c0008t0024g0001 | 2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2014-875A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | chr7 | 77950742 | ||||||
| chr7:77950810
|
A | G | 59 | a0001c0001t0001g0056a0001c0002t0002g0008a0001c0002t0002g0009others(56): Show | 59 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.2014-807A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | chr7 | 77950810 | ||||||
| chr7:77950940
|
G | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2014-677G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | chr7 | 77950940 | ||||||
| chr7:77951106
|
G | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096 | 3 | HG00735.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2014-511G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | chr7 | 77951106 | ||||||
| chr7:77951193
|
C | G | 1 | a0001c0001t0019g0066 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2014-424C>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | chr7 | 77951193 | ||||||
| chr7:77951238
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2014-379A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | chr7 | 77951238 | ||||||
| chr7:77951242
|
C | T | 1 | a0001c0002t0002g0046 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2014-375C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | chr7 | 77951242 | ||||||
| chr7:77951257
|
A | C | 1 | a0001c0001t0001g0154 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2014-360A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | chr7 | 77951257 | ||||||
| chr7:77951258
|
G | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG00621.hp1 NA18983.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.2014-359G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | chr7 | 77951258 | ||||||
| chr7:77951414
|
T | TTTTTTTT others(3227): Show |
1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2014-201_2014-200i others(3236): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 77951414 | |||||
| chr7:77951422
|
C | T | 1 | a0001c0001t0001g0224 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2014-195C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 16/18 | chr7 | 77951422 | ||||||
| chr7:77951725
|
C | T | 16 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(13): Show | 16 | HG00140.hp1 HG00642.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.2109+13C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 17/18 | chr7 | 77951725 | ||||||
| chr7:77952515
|
C | T | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2109+803C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 17/18 | chr7 | 77952515 | ||||||
| chr7:77952657
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2109+945G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 17/18 | chr7 | 77952657 | ||||||
| chr7:77952699
|
A | G | 2 | a0001c0001t0001g0284a0001c0001t0001g0287 | 2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2109+987A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 17/18 | chr7 | 77952699 | ||||||
| chr7:77952812
|
A | G | 2 | a0001c0002t0001g0289a0001c0002t0016g0290 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2110-957A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 17/18 | chr7 | 77952812 | ||||||
| chr7:77952903
|
T | C | 5 | a0001c0002t0013g0294a0001c0002t0020g0293a0001c0004t0007g0017others(2): Show | 5 | HG01099.hp1 HG02572.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2110-866T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 17/18 | chr7 | 77952903 | ||||||
| chr7:77952918
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2110-851G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 17/18 | chr7 | 77952918 | ||||||
| chr7:77952948
|
T | C | 99 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.2110-821T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 17/18 | chr7 | 77952948 | ||||||
| chr7:77953057
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2110-712C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 17/18 | chr7 | 77953057 | ||||||
| chr7:77953195
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2110-574C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 17/18 | chr7 | 77953195 | ||||||
| chr7:77953346
|
A | G | 100 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0074others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.2110-423A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 17/18 | chr7 | 77953346 | ||||||
| chr7:77953461
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2110-308C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 17/18 | chr7 | 77953461 | ||||||
| chr7:77953972
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2235+78A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77953972 | ||||||
| chr7:77954132
|
G | T | 1 | a0001c0001t0001g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2235+238G>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954132 | ||||||
| chr7:77954195
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2235+301G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954195 | ||||||
| chr7:77954219
|
T | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2235+325T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954219 | ||||||
| chr7:77954287
|
C | T | 1 | a0001c0002t0002g0033 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2235+393C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954287 | ||||||
| chr7:77954290
|
C | T | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2235+396C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954290 | ||||||
| chr7:77954301
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2235+407T>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954301 | ||||||
| chr7:77954313
|
T | C | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2235+419T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954313 | ||||||
| chr7:77954323
|
A | C | 66 | a0001c0001t0001g0056a0001c0001t0005g0025a0001c0001t0005g0026others(63): Show | 66 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.2235+429A>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954323 | ||||||
| chr7:77954425
|
C | T | 9 | a0001c0001t0001g0192a0001c0001t0001g0198a0001c0001t0001g0220others(6): Show | 9 | HG00642.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2236-433C>T | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954425 | ||||||
| chr7:77954539
|
T | C | 4 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG00639.hp2 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2236-319T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954539 | ||||||
| chr7:77954608
|
C | CTG | 8 | a0001c0001t0001g0019a0001c0001t0001g0081a0001c0001t0001g0086others(5): Show | 8 | HG01517.hp1 HG02055.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2236-246_2236-245d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954608 | |||||
| chr7:77954608
|
C | CTGTG | 3 | a0001c0001t0001g0088a0001c0002t0002g0067a0001c0002t0025g0060 | 3 | HG03654.hp1 HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2236-248_2236-245d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954608 | |||||
| chr7:77954608
|
CTG | C | 20 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0103others(17): Show | 20 | HG00438.hp1 HG01257.hp2 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.2236-246_2236-245d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954608 | |||||
| chr7:77954610
|
G | A | 1 | a0003c0008t0024g0001 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2236-248G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954610 | ||||||
| chr7:77954610
|
G | GTA | 3 | a0001c0001t0001g0020a0001c0001t0001g0173a0001c0001t0001g0214 | 3 | HG02896.hp2 NA18945.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2236-247_2236-246i others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954610 | |||||
| chr7:77954610
|
G | GTATA | 7 | a0001c0001t0001g0074a0001c0001t0001g0102a0001c0001t0001g0118others(4): Show | 7 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2236-247_2236-246i others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954610 | |||||
| chr7:77954610
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0130 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2236-247_2236-246i others(12): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954610 | |||||
| chr7:77954610
|
GTGTA | G | 41 | a0001c0001t0001g0016a0001c0001t0001g0075a0001c0001t0001g0076others(38): Show | 41 | HG00140.hp2 HG00423.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.2236-246_2236-243d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954610 | |||||
| chr7:77954610
|
GTGTATA | G | 8 | a0001c0001t0001g0104a0001c0001t0001g0112a0001c0001t0001g0126others(5): Show | 8 | HG00735.hp2 HG02074.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.2236-246_2236-241d others(8): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954610 | |||||
| chr7:77954610
|
GTGTATAT others(3): Show |
G | 4 | a0001c0001t0001g0129a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | HG01243.hp2 HG02280.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2236-246_2236-237d others(12): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954610 | |||||
| chr7:77954612
|
G | A | 23 | a0001c0001t0001g0020a0001c0001t0001g0074a0001c0001t0001g0100others(20): Show | 23 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.2236-246G>A | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954612 | ||||||
| chr7:77954612
|
G | GTA | 40 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(37): Show | 40 | HG00423.hp1 HG00741.hp1 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.2236-213_2236-212d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTATA | 5 | a0001c0001t0001g0268a0001c0001t0001g0283a0001c0001t0001g0313others(2): Show | 5 | HG01255.hp2 HG01884.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2236-215_2236-212d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTATATA | 3 | a0001c0001t0001g0252a0001c0001t0001g0279a0001c0001t0001g0282 | 3 | HG02896.hp1 HG02897.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2236-217_2236-212d others(8): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTATATAT others(1): Show |
3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0286 | 3 | HG01257.hp1 HG01258.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2236-219_2236-212d others(10): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0233 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2236-221_2236-212d others(12): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTATATAT others(11): Show |
1 | a0001c0001t0010g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2236-229_2236-212d others(20): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTGTA | 6 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0087others(3): Show | 6 | HG00280.hp1 HG00735.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2236-245_2236-244i others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTGTATA | 8 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0178others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2236-245_2236-244i others(8): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTGTATAT others(1): Show |
8 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(5): Show | 8 | HG02109.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2236-245_2236-244i others(10): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTGTATAT others(3): Show |
8 | a0001c0001t0001g0175a0001c0001t0001g0181a0001c0001t0001g0188others(5): Show | 8 | HG00642.hp2 HG01192.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.2236-245_2236-244i others(12): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTGTATAT others(5): Show |
2 | a0001c0001t0001g0187a0001c0001t0017g0071 | 2 | HG02257.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2236-245_2236-244i others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTGTGTA | 9 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0010others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.2236-245_2236-244i others(8): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTGTGTAT others(1): Show |
4 | a0001c0002t0002g0037a0001c0002t0002g0044a0001c0002t0002g0046others(1): Show | 4 | HG04204.hp2 NA18969.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.2236-245_2236-244i others(10): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTGTGTAT others(3): Show |
10 | a0001c0001t0001g0056a0001c0002t0002g0022a0001c0002t0002g0028others(7): Show | 10 | HG00741.hp2 HG01099.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.2236-245_2236-244i others(12): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTGTGTAT others(5): Show |
13 | a0001c0002t0002g0021a0001c0002t0002g0039a0001c0002t0002g0040others(10): Show | 13 | HG01358.hp2 HG02615.hp1 HG03225.hp1 others(10): Show |
intron_variant | MODIFIER | c.2236-245_2236-244i others(14): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTGTGTAT others(7): Show |
8 | a0001c0002t0002g0041a0001c0002t0002g0043a0001c0002t0002g0062others(5): Show | 8 | HG00639.hp1 HG01074.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2236-245_2236-244i others(16): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTGTGTAT others(9): Show |
2 | a0001c0002t0002g0036a0001c0002t0002g0053 | 2 | HG02559.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.2236-245_2236-244i others(18): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTGTGTAT others(11): Show |
3 | a0001c0002t0002g0061a0001c0002t0002g0097a0001c0004t0007g0069 | 3 | HG00733.hp1 HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2236-245_2236-244i others(20): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
G | GTGTGTAT others(13): Show |
2 | a0001c0002t0002g0032a0001c0002t0002g0063 | 2 | HG03017.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2236-245_2236-244i others(22): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
GTA | G | 11 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0200others(8): Show | 11 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.2236-213_2236-212d others(4): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
GTATA | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0195a0001c0001t0001g0196others(4): Show | 7 | HG01109.hp2 HG01261.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.2236-215_2236-212d others(6): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
GTATATAT others(1): Show |
G | 8 | a0001c0001t0001g0105a0001c0001t0001g0132a0001c0001t0001g0133others(5): Show | 8 | HG00099.hp2 HG01109.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.2236-219_2236-212d others(10): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954612
|
GTATATAT others(11): Show |
G | 1 | a0001c0002t0002g0038 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2236-229_2236-212d others(20): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954612 | |||||
| chr7:77954614
|
A | G | 10 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0090others(7): Show | 10 | HG00438.hp2 HG01256.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2236-244A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954614 | ||||||
| chr7:77954616
|
A | G | 5 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0200others(2): Show | 5 | HG00280.hp2 HG00323.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.2236-242A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954616 | ||||||
| chr7:77954618
|
A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0195a0001c0001t0001g0196others(2): Show | 5 | HG02027.hp1 HG02071.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.2236-240A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954618 | ||||||
| chr7:77954620
|
A | G | 1 | a0001c0002t0002g0288 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2236-238A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954620 | ||||||
| chr7:77954622
|
A | G | 5 | a0001c0002t0002g0033a0001c0002t0002g0034a0001c0002t0002g0035others(2): Show | 5 | HG02135.hp1 HG03130.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.2236-236A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954622 | ||||||
| chr7:77954624
|
A | G | 4 | a0001c0002t0002g0033a0001c0002t0002g0034a0001c0002t0002g0035others(1): Show | 4 | HG02135.hp1 NA18747.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2236-234A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954624 | ||||||
| chr7:77954625
|
T | TGTATATA others(79): Show |
6 | a0001c0001t0003g0306a0001c0001t0003g0308a0001c0001t0003g0309others(3): Show | 6 | HG02055.hp2 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2236-233_2236-232i others(88): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954625 | ||||||
| chr7:77954626
|
A | G | 7 | a0001c0001t0003g0306a0001c0001t0003g0307a0001c0001t0003g0308others(4): Show | 7 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2236-232A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954626 | ||||||
| chr7:77954628
|
A | ATATATAT others(77): Show |
1 | a0001c0001t0003g0307 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2236-212_2236-211i others(86): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954628 | |||||
| chr7:77954632
|
A | G | 1 | a0001c0002t0002g0038 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2236-226A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954632 | ||||||
| chr7:77954634
|
A | G | 1 | a0001c0002t0002g0038 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2236-224A>G | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954634 | ||||||
| chr7:77954637
|
T | TATATAG | 3 | a0001c0003t0004g0003a0001c0003t0004g0005a0001c0003t0004g0006 | 3 | HG00642.hp1 HG01256.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2236-216_2236-215i others(8): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954637 | |||||
| chr7:77954637
|
T | TATATATA others(3): Show |
1 | a0001c0003t0004g0004 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2236-220_2236-211d others(12): Show |
PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954637 | |||||
| chr7:77954643
|
T | C | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2236-215T>C | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | chr7 | 77954643 | ||||||
| chr7:77954842
|
A | AT | 71 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0030others(68): Show | 71 | HG00639.hp1 HG00733.hp1 HG00741.hp2 others(68): Show |
splice_region_variant&intron_variant | LOW | c.2236-5dupT | PHTF2 | ENSG00000006576.17 | transcript | ENST00000422959.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr7 | 77954842 |