Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 100507421 |
|---|---|
| ensemblid | ENSG00000261115.7 |
| hgncid | 44112 |
| symbol | TMEM178B |
| name | transmembrane protein 178B |
| refseq_nuc | NM_001195278.2 |
| refseq_prot | NP_001182207.1 |
| ensembl_nuc | ENST00000565468.6 |
| ensembl_prot | ENSP00000456594.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 141074064 |
| end | 141480380 |
| strand | + |
| ver | v1.2 |
| region | chr7:141074064-141480380 |
| region5000 | chr7:141069064-141485380 |
| regionname0 | TMEM178B_chr7_141074064_141480380 |
| regionname5000 | TMEM178B_chr7_141069064_141485380 |
| 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 | 0/0 | 294 | 79 | 51 | 14 | 8 | 0 | 6 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0002 | 0/0 | 294 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 885 | 39 | 30 | 4 | 2 | 0 | 3 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| c0002 | 0/0 | 885 | 33 | 19 | 7 | 5 | 0 | 2 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| c0003 | 0/0 | 885 | 5 | 1 | 3 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| c0004 | 0/0 | 885 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| c0005 | 0/0 | 885 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| c0006 | 0/0 | 885 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 9838 | 15 | 5 | 6 | 2 | 0 | 2 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0002 | 0/0 | 9826 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0003 | 0/0 | 9830 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0004 | 0/0 | 9830 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0005 | 0/0 | 9838 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0006 | 0/0 | 9842 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0007 | 0/0 | 9842 | 3 | 1 | 0 | 0 | 0 | 2 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0008 | 0/0 | 9842 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0009 | 0/0 | 9838 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0010 | 0/0 | 9825 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0011 | 0/0 | 9838 | 2 | 1 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0012 | 0/0 | 9842 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0013 | 0/0 | 9842 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0014 | 0/0 | 9842 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0015 | 0/0 | 9844 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0016 | 0/0 | 9840 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0017 | 0/0 | 9826 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0018 | 0/0 | 9838 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0019 | 0/0 | 9838 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0020 | 0/0 | 9840 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0021 | 0/0 | 9840 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0022 | 0/0 | 9842 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0023 | 0/0 | 9843 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0024 | 0/0 | 9825 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0025 | 0/0 | 9825 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0026 | 0/0 | 9826 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0027 | 0/0 | 9826 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0028 | 0/0 | 9835 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0029 | 0/0 | 9837 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0030 | 0/0 | 9840 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0031 | 0/0 | 9842 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0032 | 0/0 | 9842 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0033 | 0/0 | 9842 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0034 | 0/0 | 9842 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0035 | 0/0 | 9841 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0036 | 0/0 | 9844 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0037 | 0/0 | 9844 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0038 | 0/0 | 9840 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0039 | 0/0 | 9840 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0040 | 0/0 | 9840 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0041 | 0/0 | 9838 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0042 | 0/0 | 9830 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0043 | 0/0 | 9843 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| t0044 | 0/0 | 9845 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| 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 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 885 | 39 | 30 | 4 | 2 | 0 | 3 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002 | 0/0 | 885 | 33 | 19 | 7 | 5 | 0 | 2 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0003 | 0/0 | 885 | 5 | 1 | 3 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0004 | 0/0 | 885 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0005 | 0/0 | 885 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0002c0006 | 0/0 | 885 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 10722 | 5 | 2 | 1 | 1 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0002 | 0/0 | 10710 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0003 | 0/0 | 10714 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0004 | 0/0 | 10714 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0005 | 0/0 | 10722 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0006 | 0/0 | 10726 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0007 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0008 | 0/0 | 10726 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0009 | 0/0 | 10722 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0010 | 0/0 | 10709 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0011 | 0/0 | 10722 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0012 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0014 | 0/0 | 10726 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0015 | 0/0 | 10728 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0016 | 0/0 | 10724 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0020 | 0/0 | 10724 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0021 | 0/0 | 10724 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0022 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0023 | 0/0 | 10727 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0025 | 0/0 | 10709 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0028 | 0/0 | 10719 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0029 | 0/0 | 10721 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0033 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0034 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0035 | 0/0 | 10725 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0038 | 0/0 | 10724 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0001t0044 | 0/0 | 10729 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0001 | 0/0 | 10722 | 6 | 3 | 3 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0002 | 0/0 | 10710 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0003 | 0/0 | 10714 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0005 | 0/0 | 10722 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0006 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0007 | 0/0 | 10726 | 2 | 1 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0008 | 0/0 | 10726 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0009 | 0/0 | 10722 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0010 | 0/0 | 10709 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0011 | 0/0 | 10722 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0012 | 0/0 | 10726 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0013 | 0/0 | 10726 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0015 | 0/0 | 10728 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0016 | 0/0 | 10724 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0017 | 0/0 | 10710 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0024 | 0/0 | 10709 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0026 | 0/0 | 10710 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0027 | 0/0 | 10710 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0030 | 0/0 | 10724 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0031 | 0/0 | 10726 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0032 | 0/0 | 10726 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0036 | 0/0 | 10728 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0037 | 0/0 | 10728 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0040 | 0/0 | 10724 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0041 | 0/0 | 10722 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0002t0042 | 0/0 | 10714 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0003t0001 | 0/0 | 10722 | 3 | 0 | 2 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0003t0018 | 0/0 | 10722 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0003t0019 | 0/0 | 10722 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0004t0043 | 0/0 | 10727 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0001c0005t0001 | 0/0 | 10722 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| a0002c0006t0039 | 0/0 | 10724 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | copy fasta | chr7 | 141069064 | 141485380 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0007g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0008g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0010g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0011g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0012g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0014g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0014g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0015g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0016g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0020g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0021g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0022g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0023g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0025g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0028g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0029g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0033g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0034g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0035g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0038g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0001t0044g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0007g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0010g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0011g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0012g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0013g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0013g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0015g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0016g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0017g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0024g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0026g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0027g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0030g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0031g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0032g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0036g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0037g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0040g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0041g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0002t0042g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0003t0018g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0003t0019g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0004t0043g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0001c0005t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| a0002c0006t0039g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG00544 | hp2 | a0001 | c0002 | t0013 | g0047 | EAS | CHS | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0074 | AMR | PUR | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01243 | hp1 | a0001 | c0001 | t0014 | g0033 | AMR | PUR | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0068 | AMR | PUR | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01255 | hp1 | a0001 | c0002 | t0032 | g0071 | AMR | CLM | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01255 | hp2 | a0001 | c0002 | t0013 | g0059 | AMR | CLM | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01256 | hp1 | a0001 | c0003 | t0018 | g0046 | AMR | CLM | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01256 | hp2 | a0001 | c0002 | t0036 | g0069 | AMR | CLM | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01261 | hp1 | a0001 | c0001 | t0022 | g0013 | AMR | CLM | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01261 | hp2 | a0001 | c0002 | t0016 | g0072 | AMR | CLM | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01884 | hp1 | a0001 | c0003 | t0019 | g0070 | AFR | ACB | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01884 | hp2 | a0001 | c0001 | t0029 | g0026 | AFR | ACB | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01891 | hp1 | a0001 | c0001 | t0016 | g0037 | AFR | ACB | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0052 | AFR | ACB | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PEL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0023 | AMR | PEL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | PEL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | PEL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02027 | hp1 | a0001 | c0002 | t0041 | g0058 | EAS | KHV | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02027 | hp2 | a0001 | c0002 | t0037 | g0075 | EAS | KHV | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02083 | hp1 | a0001 | c0002 | t0011 | g0044 | EAS | KHV | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02083 | hp2 | a0001 | c0002 | t0012 | g0045 | EAS | KHV | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02258 | hp1 | a0001 | c0001 | t0035 | g0079 | AFR | ACB | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02523 | hp1 | a0001 | c0003 | t0001 | g0055 | EAS | KHV | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02523 | hp2 | a0001 | c0001 | t0012 | g0036 | EAS | KHV | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02572 | hp1 | a0001 | c0002 | t0026 | g0041 | AFR | GWD | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02572 | hp2 | a0001 | c0001 | t0011 | g0016 | AFR | GWD | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02602 | hp1 | a0001 | c0002 | t0007 | g0073 | SAS | PJL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02602 | hp2 | a0001 | c0002 | t0031 | g0063 | SAS | PJL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0039 | AFR | GWD | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02630 | hp1 | a0001 | c0001 | t0033 | g0031 | AFR | GWD | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02630 | hp2 | a0001 | c0002 | t0006 | g0040 | AFR | GWD | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0030 | AFR | GWD | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0078 | AFR | GWD | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02683 | hp2 | a0001 | c0001 | t0020 | g0006 | SAS | PJL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02922 | hp1 | a0001 | c0001 | t0038 | g0034 | AFR | ESN | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ESN | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03130 | hp1 | a0001 | c0001 | t0034 | g0009 | AFR | ESN | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | ESN | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | ESN | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | ESN | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03209 | hp1 | a0001 | c0002 | t0040 | g0050 | AFR | MSL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03225 | hp1 | a0002 | c0006 | t0039 | g0061 | AFR | MSL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03225 | hp2 | a0001 | c0002 | t0015 | g0056 | AFR | MSL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03453 | hp1 | a0001 | c0001 | t0044 | g0001 | AFR | MSL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | MSL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03486 | hp1 | a0001 | c0001 | t0028 | g0022 | AFR | MSL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03486 | hp2 | a0001 | c0002 | t0009 | g0060 | AFR | MSL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03516 | hp1 | a0001 | c0001 | t0010 | g0021 | AFR | ESN | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03516 | hp2 | a0001 | c0001 | t0015 | g0028 | AFR | ESN | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03540 | hp1 | a0001 | c0002 | t0017 | g0062 | AFR | GWD | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03540 | hp2 | a0001 | c0002 | t0027 | g0051 | AFR | GWD | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03579 | hp1 | a0001 | c0002 | t0008 | g0003 | AFR | MSL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03579 | hp2 | a0001 | c0002 | t0010 | g0066 | AFR | MSL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03704 | hp1 | a0001 | c0001 | t0007 | g0011 | SAS | PJL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03704 | hp2 | a0001 | c0005 | t0001 | g0005 | SAS | PJL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| NA18522 | hp1 | a0001 | c0002 | t0024 | g0002 | AFR | YRI | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0043 | AFR | YRI | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | LWK | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | LWK | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | LWK | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| NA19043 | hp2 | a0001 | c0002 | t0005 | g0049 | AFR | LWK | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02109 | hp1 | a0001 | c0002 | t0030 | g0067 | AFR | ACB | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02109 | hp2 | a0001 | c0004 | t0043 | g0032 | AFR | ACB | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02486 | hp1 | a0001 | c0001 | t0025 | g0010 | AFR | ACB | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | ACB | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| HG03471 | hp2 | a0001 | c0001 | t0021 | g0077 | AFR | MSL | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | USA | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| NA20300 | hp2 | a0001 | c0002 | t0007 | g0053 | AFR | USA | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| NA21309 | hp1 | a0001 | c0001 | t0023 | g0018 | AFR | LWK | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| NA21309 | hp2 | a0001 | c0002 | t0042 | g0054 | AFR | LWK | TMEM178B_chr7_141069064_141485380 | TMEM178B | chr7 | 141069064 | 141485380 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:141470729
|
A | C | 1 | a0002 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.828A>C | p.Gln276His | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 1075/10726 | 828/885 | 276/294 | chr7 | 141470729 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:141074667
|
C | G | 3 | a0001c0002a0001c0003a0002c0006 | 39 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(36): Show |
synonymous_variant | LOW | c.357C>G | p.Pro119Pro | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/4 | 604/10726 | 357/885 | 119/294 | chr7 | 141074667 | ||
| chr7:141437660
|
C | T | 2 | a0001c0003a0001c0005 | 6 | HG01106.hp1 HG01243.hp2 HG01256.hp1 others(3): Show |
synonymous_variant | LOW | c.549C>T | p.Leu183Leu | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/4 | 796/10726 | 549/885 | 183/294 | chr7 | 141437660 | ||
| chr7:141437675
|
C | T | 1 | a0001c0004 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.564C>T | p.Ile188Ile | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/4 | 811/10726 | 564/885 | 188/294 | chr7 | 141437675 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:141470819
|
A | AAT | 4 | a0001c0001t0016a0001c0001t0044a0001c0002t0016others(1): Show | 4 | HG01261.hp2 HG01891.hp1 HG02109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*45_*46dupTA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 47 | INFO_REALIGN_3_PRIME | chr7 | 141470819 | ||||
| chr7:141471045
|
G | A | 2 | a0001c0001t0044a0001c0004t0043 | 2 | HG02109.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*259G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 259 | chr7 | 141471045 | |||||
| chr7:141471059
|
A | T | 1 | a0001c0002t0042 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*273A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 273 | chr7 | 141471059 | |||||
| chr7:141471159
|
C | T | 1 | a0001c0002t0041 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 373 | chr7 | 141471159 | |||||
| chr7:141471427
|
C | T | 2 | a0001c0001t0044a0001c0004t0043 | 2 | HG02109.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*641C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 641 | chr7 | 141471427 | |||||
| chr7:141471560
|
G | A | 13 | a0001c0001t0001a0001c0001t0009a0001c0001t0020others(10): Show | 24 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*774G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 774 | chr7 | 141471560 | |||||
| chr7:141471779
|
TGC | T | 4 | a0001c0001t0038a0001c0002t0040a0001c0004t0043others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*995_*996delCG | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 995 | INFO_REALIGN_3_PRIME | chr7 | 141471779 | ||||
| chr7:141471781
|
C | CGT | 4 | a0001c0001t0015a0001c0002t0015a0001c0002t0036others(1): Show | 4 | HG01256.hp2 HG02027.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1031_*1032dupTG | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 1033 | INFO_REALIGN_3_PRIME | chr7 | 141471781 | ||||
| chr7:141471781
|
C | T | 1 | a0001c0001t0044 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*995C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 995 | chr7 | 141471781 | |||||
| chr7:141471781
|
CGT | C | 3 | a0001c0001t0020a0001c0001t0021a0001c0002t0030 | 3 | HG02109.hp1 HG02683.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1031_*1032delTG | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 1031 | INFO_REALIGN_3_PRIME | chr7 | 141471781 | ||||
| chr7:141471781
|
CGTGT | C | 15 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(12): Show | 27 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1029_*1032delTGTG | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 1029 | INFO_REALIGN_3_PRIME | chr7 | 141471781 | ||||
| chr7:141471781
|
CGTGTGT | C | 2 | a0001c0001t0028a0001c0001t0029 | 2 | HG01884.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1027_*1032delTGTG others(2): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 1027 | INFO_REALIGN_3_PRIME | chr7 | 141471781 | ||||
| chr7:141471781
|
CGTGTGTG others(5): Show |
C | 4 | a0001c0001t0003a0001c0001t0004a0001c0002t0003others(1): Show | 7 | HG01891.hp2 HG01952.hp2 HG02897.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1021_*1032delTGTG others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 1021 | INFO_REALIGN_3_PRIME | chr7 | 141471781 | ||||
| chr7:141471781
|
CGTGTGTG others(9): Show |
C | 9 | a0001c0001t0002a0001c0001t0010a0001c0001t0025others(6): Show | 10 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1017_*1032delTGTG others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 1017 | INFO_REALIGN_3_PRIME | chr7 | 141471781 | ||||
| chr7:141471783
|
T | C | 1 | a0001c0001t0044 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*997T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 997 | chr7 | 141471783 | |||||
| chr7:141471785
|
T | C | 4 | a0001c0001t0038a0001c0002t0040a0001c0004t0043others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*999T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 999 | chr7 | 141471785 | |||||
| chr7:141471787
|
T | C | 1 | a0001c0001t0023 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1001T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 1001 | chr7 | 141471787 | |||||
| chr7:141472167
|
C | T | 6 | a0001c0001t0023a0001c0001t0038a0001c0001t0044others(3): Show | 6 | HG02109.hp2 HG02922.hp1 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1381C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 1381 | chr7 | 141472167 | |||||
| chr7:141472404
|
G | A | 6 | a0001c0001t0023a0001c0001t0038a0001c0001t0044others(3): Show | 6 | HG02109.hp2 HG02922.hp1 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1618G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 1618 | chr7 | 141472404 | |||||
| chr7:141472528
|
C | T | 1 | a0001c0001t0029 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1742C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 1742 | chr7 | 141472528 | |||||
| chr7:141472674
|
A | G | 41 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(38): Show | 57 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1888A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 1888 | chr7 | 141472674 | |||||
| chr7:141472895
|
G | C | 1 | a0001c0001t0038 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2109G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 2109 | chr7 | 141472895 | |||||
| chr7:141472913
|
A | G | 8 | a0001c0001t0016a0001c0001t0023a0001c0001t0038others(5): Show | 8 | HG01261.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2127A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 2127 | chr7 | 141472913 | |||||
| chr7:141473020
|
G | A | 1 | a0001c0002t0031 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2234G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 2234 | chr7 | 141473020 | |||||
| chr7:141473277
|
C | T | 12 | a0001c0001t0002a0001c0001t0010a0001c0001t0015others(9): Show | 13 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2491C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 2491 | chr7 | 141473277 | |||||
| chr7:141473297
|
G | A | 1 | a0001c0003t0019 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2511G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 2511 | chr7 | 141473297 | |||||
| chr7:141473319
|
C | T | 13 | a0001c0001t0002a0001c0001t0010a0001c0001t0015others(10): Show | 14 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2533C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 2533 | chr7 | 141473319 | |||||
| chr7:141473320
|
A | G | 27 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(24): Show | 32 | HG01243.hp1 HG01261.hp2 HG01884.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2534A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 2534 | chr7 | 141473320 | |||||
| chr7:141473596
|
C | CT | 3 | a0001c0001t0023a0001c0001t0044a0001c0004t0043 | 3 | HG02109.hp2 HG03453.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2813dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 2814 | INFO_REALIGN_3_PRIME | chr7 | 141473596 | ||||
| chr7:141473645
|
C | T | 2 | a0001c0002t0040a0002c0006t0039 | 2 | HG03209.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2859C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 2859 | chr7 | 141473645 | |||||
| chr7:141474263
|
C | A | 3 | a0001c0001t0035a0001c0001t0038a0001c0002t0024 | 3 | HG02258.hp1 HG02922.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3477C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 3477 | chr7 | 141474263 | |||||
| chr7:141474597
|
G | A | 2 | a0001c0001t0035a0001c0001t0038 | 2 | HG02258.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3811G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 3811 | chr7 | 141474597 | |||||
| chr7:141474688
|
T | C | 2 | a0001c0002t0040a0002c0006t0039 | 2 | HG03209.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3902T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 3902 | chr7 | 141474688 | |||||
| chr7:141474733
|
C | T | 13 | a0001c0001t0002a0001c0001t0010a0001c0001t0015others(10): Show | 14 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3947C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 3947 | chr7 | 141474733 | |||||
| chr7:141475191
|
A | G | 1 | a0001c0001t0014 | 2 | HG01243.hp1 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4405A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 4405 | chr7 | 141475191 | |||||
| chr7:141475298
|
A | C | 1 | a0001c0002t0024 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4512A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 4512 | chr7 | 141475298 | |||||
| chr7:141475471
|
A | G | 7 | a0001c0001t0003a0001c0001t0004a0001c0001t0029others(4): Show | 10 | HG01884.hp2 HG01891.hp2 HG01952.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4685A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 4685 | chr7 | 141475471 | |||||
| chr7:141475509
|
C | T | 2 | a0001c0001t0005a0001c0002t0005 | 3 | HG02922.hp2 HG03139.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4723C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 4723 | chr7 | 141475509 | |||||
| chr7:141475609
|
G | A | 4 | a0001c0001t0028a0001c0001t0035a0001c0001t0038others(1): Show | 4 | HG02258.hp1 HG02922.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4823G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 4823 | chr7 | 141475609 | |||||
| chr7:141475668
|
C | T | 2 | a0001c0001t0035a0001c0001t0038 | 2 | HG02258.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4882C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 4882 | chr7 | 141475668 | |||||
| chr7:141475788
|
CT | C | 13 | a0001c0001t0002a0001c0001t0010a0001c0001t0015others(10): Show | 14 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5013delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 5013 | INFO_REALIGN_3_PRIME | chr7 | 141475788 | ||||
| chr7:141475916
|
A | T | 7 | a0001c0001t0005a0001c0001t0020a0001c0001t0022others(4): Show | 9 | HG00544.hp2 HG01255.hp2 HG01256.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5130A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 5130 | chr7 | 141475916 | |||||
| chr7:141476385
|
C | T | 2 | a0001c0002t0026a0001c0002t0027 | 2 | HG02572.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5599C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 5599 | chr7 | 141476385 | |||||
| chr7:141476454
|
A | G | 1 | a0001c0002t0024 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5668A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 5668 | chr7 | 141476454 | |||||
| chr7:141476696
|
A | T | 1 | a0001c0002t0040 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5910A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 5910 | chr7 | 141476696 | |||||
| chr7:141476731
|
C | T | 4 | a0001c0001t0002a0001c0001t0010a0001c0002t0002others(1): Show | 5 | HG02615.hp1 HG03471.hp1 HG03516.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5945C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 5945 | chr7 | 141476731 | |||||
| chr7:141477128
|
G | A | 5 | a0001c0001t0009a0001c0001t0011a0001c0002t0009others(2): Show | 5 | HG02027.hp2 HG02083.hp1 HG02572.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6342G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 6342 | chr7 | 141477128 | |||||
| chr7:141477141
|
C | T | 1 | a0001c0002t0027 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6355C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 6355 | chr7 | 141477141 | |||||
| chr7:141477188
|
T | C | 28 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(25): Show | 33 | HG01243.hp1 HG01261.hp2 HG01884.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*6402T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 6402 | chr7 | 141477188 | |||||
| chr7:141477350
|
G | A | 2 | a0001c0001t0015a0001c0002t0015 | 2 | HG03225.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6564G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 6564 | chr7 | 141477350 | |||||
| chr7:141477362
|
C | T | 2 | a0001c0001t0035a0001c0001t0038 | 2 | HG02258.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6576C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 6576 | chr7 | 141477362 | |||||
| chr7:141477363
|
G | A | 2 | a0001c0001t0012a0001c0002t0012 | 2 | HG02083.hp2 HG02523.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6577G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 6577 | chr7 | 141477363 | |||||
| chr7:141477392
|
A | C | 57 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(54): Show | 77 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*6606A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 6606 | chr7 | 141477392 | |||||
| chr7:141477984
|
G | T | 1 | a0001c0001t0023 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7198G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 7198 | chr7 | 141477984 | |||||
| chr7:141478136
|
G | A | 1 | a0001c0002t0024 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7350G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 7350 | chr7 | 141478136 | |||||
| chr7:141478586
|
G | C | 1 | a0001c0001t0034 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7800G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 7800 | chr7 | 141478586 | |||||
| chr7:141478840
|
T | TG | 8 | a0001c0001t0002a0001c0001t0015a0001c0001t0029others(5): Show | 9 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8062dupG | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 8063 | INFO_REALIGN_3_PRIME | chr7 | 141478840 | ||||
| chr7:141478868
|
C | T | 1 | a0001c0001t0028 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8082C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 8082 | chr7 | 141478868 | |||||
| chr7:141479196
|
G | A | 4 | a0001c0001t0023a0001c0001t0044a0001c0004t0043others(1): Show | 4 | HG02109.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8410G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 8410 | chr7 | 141479196 | |||||
| chr7:141479311
|
T | G | 13 | a0001c0001t0002a0001c0001t0014a0001c0001t0015others(10): Show | 15 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*8525T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 8525 | chr7 | 141479311 | |||||
| chr7:141479763
|
T | C | 15 | a0001c0001t0002a0001c0001t0014a0001c0001t0015others(12): Show | 17 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*8977T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 8977 | chr7 | 141479763 | |||||
| chr7:141479880
|
C | T | 3 | a0001c0001t0004a0001c0002t0040a0001c0002t0042 | 5 | HG01952.hp2 HG03130.hp2 HG03209.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9094C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 9094 | chr7 | 141479880 | |||||
| chr7:141480250
|
T | C | 51 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(48): Show | 70 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*9464T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 4/4 | 9464 | chr7 | 141480250 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:141075024
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.382+332A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141075024 | ||||||
| chr7:141075311
|
C | A | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.382+619C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141075311 | ||||||
| chr7:141075530
|
C | T | 3 | a0001c0001t0009g0078a0001c0001t0021g0077a0001c0001t0035g0079 | 3 | HG02258.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.382+838C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141075530 | ||||||
| chr7:141075702
|
T | C | 2 | a0001c0002t0008g0003a0001c0002t0024g0002 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.382+1010T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141075702 | ||||||
| chr7:141076025
|
A | G | 39 | a0001c0002t0001g0042a0001c0002t0001g0048a0001c0002t0001g0057others(36): Show | 39 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.382+1333A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141076025 | ||||||
| chr7:141076129
|
G | A | 2 | a0001c0002t0006g0040a0001c0002t0026g0041 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.382+1437G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141076129 | ||||||
| chr7:141076201
|
G | C | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+1509G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141076201 | ||||||
| chr7:141076218
|
C | A | 35 | a0001c0002t0001g0048a0001c0002t0001g0057a0001c0002t0001g0064others(32): Show | 35 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.382+1526C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141076218 | ||||||
| chr7:141076247
|
T | C | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+1555T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141076247 | ||||||
| chr7:141076601
|
T | C | 39 | a0001c0002t0001g0042a0001c0002t0001g0048a0001c0002t0001g0057others(36): Show | 39 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.382+1909T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141076601 | ||||||
| chr7:141076814
|
G | A | 39 | a0001c0002t0001g0042a0001c0002t0001g0048a0001c0002t0001g0057others(36): Show | 39 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.382+2122G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141076814 | ||||||
| chr7:141077230
|
C | T | 50 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0004g0029others(47): Show | 50 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.382+2538C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141077230 | ||||||
| chr7:141078062
|
G | A | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382+3370G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141078062 | ||||||
| chr7:141078513
|
A | G | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+3821A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141078513 | ||||||
| chr7:141078624
|
G | A | 11 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0004g0029others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.382+3932G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141078624 | ||||||
| chr7:141078792
|
T | C | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+4100T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141078792 | ||||||
| chr7:141078837
|
T | TG | 8 | a0001c0001t0001g0012a0001c0001t0003g0007a0001c0001t0005g0008others(5): Show | 8 | HG01106.hp2 HG02486.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.382+4146dupG | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141078837 | |||||
| chr7:141078932
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0007g0011 | 2 | HG01106.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.382+4240A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141078932 | ||||||
| chr7:141079148
|
A | G | 6 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0004g0024others(3): Show | 6 | HG01884.hp2 HG01952.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+4456A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141079148 | ||||||
| chr7:141079332
|
A | G | 1 | a0001c0002t0037g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.382+4640A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141079332 | ||||||
| chr7:141079671
|
C | T | 1 | a0001c0001t0028g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.382+4979C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141079671 | ||||||
| chr7:141079940
|
T | C | 78 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(75): Show | 78 | HG00544.hp2 HG01106.hp1 HG01106.hp2 others(75): Show |
intron_variant | MODIFIER | c.382+5248T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141079940 | ||||||
| chr7:141079941
|
G | A | 1 | a0001c0002t0002g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.382+5249G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141079941 | ||||||
| chr7:141080090
|
A | G | 7 | a0001c0002t0007g0073a0001c0002t0016g0072a0001c0002t0032g0071others(4): Show | 7 | HG01106.hp1 HG01243.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.382+5398A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141080090 | ||||||
| chr7:141080141
|
C | T | 1 | a0001c0002t0001g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.382+5449C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141080141 | ||||||
| chr7:141080175
|
C | T | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.382+5483C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141080175 | ||||||
| chr7:141080894
|
T | C | 35 | a0001c0002t0001g0048a0001c0002t0001g0057a0001c0002t0001g0064others(32): Show | 35 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.382+6202T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141080894 | ||||||
| chr7:141081026
|
T | C | 11 | a0001c0001t0001g0015a0001c0001t0002g0027a0001c0001t0004g0023others(8): Show | 11 | HG01261.hp1 HG01884.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.382+6334T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141081026 | ||||||
| chr7:141081108
|
T | G | 47 | a0001c0001t0001g0012a0001c0001t0003g0007a0001c0001t0005g0008others(44): Show | 47 | HG00544.hp2 HG01106.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.382+6416T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141081108 | ||||||
| chr7:141081155
|
A | G | 47 | a0001c0001t0001g0012a0001c0001t0003g0007a0001c0001t0005g0008others(44): Show | 47 | HG00544.hp2 HG01106.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.382+6463A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141081155 | ||||||
| chr7:141081156
|
C | T | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.382+6464C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141081156 | ||||||
| chr7:141081188
|
A | G | 62 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0038others(59): Show | 62 | HG00544.hp2 HG01106.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.382+6496A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141081188 | ||||||
| chr7:141081664
|
A | T | 1 | a0001c0001t0014g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.382+6972A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141081664 | ||||||
| chr7:141081701
|
A | T | 3 | a0001c0002t0001g0042a0001c0002t0006g0040a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.382+7009A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141081701 | ||||||
| chr7:141082178
|
A | G | 2 | a0001c0002t0006g0040a0001c0002t0026g0041 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.382+7486A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141082178 | ||||||
| chr7:141082239
|
G | T | 47 | a0001c0001t0001g0012a0001c0001t0003g0007a0001c0001t0005g0008others(44): Show | 47 | HG00544.hp2 HG01106.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.382+7547G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141082239 | ||||||
| chr7:141082435
|
G | A | 47 | a0001c0001t0001g0012a0001c0001t0003g0007a0001c0001t0005g0008others(44): Show | 47 | HG00544.hp2 HG01106.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.382+7743G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141082435 | ||||||
| chr7:141082504
|
C | T | 11 | a0001c0001t0001g0015a0001c0001t0002g0027a0001c0001t0004g0023others(8): Show | 11 | HG01261.hp1 HG01884.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.382+7812C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141082504 | ||||||
| chr7:141083490
|
G | A | 5 | a0001c0002t0001g0048a0001c0002t0011g0044a0001c0002t0012g0045others(2): Show | 5 | HG00544.hp2 HG01256.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+8798G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141083490 | ||||||
| chr7:141083503
|
G | C | 1 | a0001c0001t0004g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.382+8811G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141083503 | ||||||
| chr7:141083503
|
G | GAGAC | 34 | a0001c0002t0001g0048a0001c0002t0001g0057a0001c0002t0001g0064others(31): Show | 34 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.382+8835_382+8838d others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141083503 | |||||
| chr7:141083582
|
A | G | 33 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(30): Show | 33 | HG00544.hp1 HG01243.hp1 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.382+8890A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141083582 | ||||||
| chr7:141083628
|
C | T | 1 | a0001c0002t0001g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.382+8936C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141083628 | ||||||
| chr7:141083883
|
AT | A | 79 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(76): Show | 79 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(76): Show |
intron_variant | MODIFIER | c.382+9206delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141083883 | |||||
| chr7:141084239
|
T | A | 26 | a0001c0002t0001g0048a0001c0002t0001g0057a0001c0002t0002g0043others(23): Show | 26 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.382+9547T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141084239 | ||||||
| chr7:141084492
|
C | A | 2 | a0001c0002t0006g0040a0001c0002t0026g0041 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.382+9800C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141084492 | ||||||
| chr7:141084558
|
C | T | 15 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0004g0029others(12): Show | 15 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.382+9866C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141084558 | ||||||
| chr7:141084720
|
G | A | 1 | a0001c0003t0001g0068 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.382+10028G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141084720 | ||||||
| chr7:141084789
|
C | T | 1 | a0001c0002t0001g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.382+10097C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141084789 | ||||||
| chr7:141084893
|
G | T | 2 | a0001c0001t0002g0019a0001c0001t0003g0020 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.382+10201G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141084893 | ||||||
| chr7:141085150
|
AT | A | 39 | a0001c0001t0001g0080a0001c0001t0002g0019a0001c0001t0003g0020others(36): Show | 39 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.382+10484delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141085150 | |||||
| chr7:141085150
|
ATT | A | 16 | a0001c0001t0001g0035a0001c0001t0004g0029a0001c0001t0008g0030others(13): Show | 16 | HG01243.hp1 HG01256.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.382+10483_382+1048 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141085150 | |||||
| chr7:141085527
|
GGTCATC | G | 2 | a0001c0002t0006g0040a0001c0002t0026g0041 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.382+10841_382+1084 others(10): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141085527 | |||||
| chr7:141085540
|
CATTT | C | 35 | a0001c0002t0001g0048a0001c0002t0001g0057a0001c0002t0001g0064others(32): Show | 35 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.382+10851_382+1085 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141085540 | |||||
| chr7:141085584
|
ATTCTGGA others(342): Show |
A | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+10893_382+1124 others(4): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085584 | ||||||
| chr7:141085849
|
G | A | 4 | a0001c0001t0009g0078a0001c0001t0021g0077a0001c0001t0035g0079others(1): Show | 4 | HG02258.hp1 HG02647.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+11157G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085849 | ||||||
| chr7:141085936
|
A | C | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11244A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085936 | ||||||
| chr7:141085937
|
A | C | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11245A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085937 | ||||||
| chr7:141085939
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11247A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085939 | ||||||
| chr7:141085946
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11254A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085946 | ||||||
| chr7:141085947
|
G | C | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11255G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085947 | ||||||
| chr7:141085952
|
A | T | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11260A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085952 | ||||||
| chr7:141085954
|
A | C | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11262A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085954 | ||||||
| chr7:141085958
|
T | A | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11266T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085958 | ||||||
| chr7:141085962
|
T | G | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11270T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085962 | ||||||
| chr7:141085975
|
A | C | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11283A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085975 | ||||||
| chr7:141085980
|
T | G | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11288T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085980 | ||||||
| chr7:141085982
|
G | C | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11290G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085982 | ||||||
| chr7:141085983
|
T | A | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11291T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085983 | ||||||
| chr7:141085986
|
A | T | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11294A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085986 | ||||||
| chr7:141085987
|
T | A | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11295T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085987 | ||||||
| chr7:141085989
|
C | A | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11297C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085989 | ||||||
| chr7:141085991
|
T | C | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11299T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085991 | ||||||
| chr7:141085997
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11305A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085997 | ||||||
| chr7:141085999
|
A | T | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11307A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141085999 | ||||||
| chr7:141086002
|
T | G | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11310T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141086002 | ||||||
| chr7:141086003
|
G | T | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11311G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141086003 | ||||||
| chr7:141086009
|
G | T | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11317G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141086009 | ||||||
| chr7:141086012
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11320A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141086012 | ||||||
| chr7:141086017
|
T | C | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11325T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141086017 | ||||||
| chr7:141086018
|
G | T | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11326G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141086018 | ||||||
| chr7:141086022
|
T | C | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11330T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141086022 | ||||||
| chr7:141086024
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11332C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141086024 | ||||||
| chr7:141086026
|
T | G | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11334T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141086026 | ||||||
| chr7:141086028
|
T | A | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11336T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141086028 | ||||||
| chr7:141086029
|
ATTAATAT others(192): Show |
A | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+11338_382+1153 others(4): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141086029 | ||||||
| chr7:141086579
|
A | T | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+11887A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141086579 | ||||||
| chr7:141086869
|
A | G | 4 | a0001c0001t0003g0007a0001c0001t0005g0008a0001c0001t0025g0010others(1): Show | 4 | HG02486.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+12177A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141086869 | ||||||
| chr7:141086881
|
A | T | 36 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(33): Show | 36 | HG00544.hp1 HG01243.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.382+12189A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141086881 | ||||||
| chr7:141086918
|
C | T | 2 | a0001c0002t0006g0040a0001c0002t0026g0041 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.382+12226C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141086918 | ||||||
| chr7:141086978
|
G | A | 2 | a0001c0002t0011g0044a0001c0002t0012g0045 | 2 | HG02083.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.382+12286G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141086978 | ||||||
| chr7:141087088
|
T | TA | 4 | a0001c0001t0009g0078a0001c0001t0021g0077a0001c0001t0035g0079others(1): Show | 4 | HG02258.hp1 HG02647.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+12402dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141087088 | |||||
| chr7:141088413
|
A | G | 35 | a0001c0002t0001g0048a0001c0002t0001g0057a0001c0002t0001g0064others(32): Show | 35 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.382+13721A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141088413 | ||||||
| chr7:141088518
|
C | T | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.382+13826C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141088518 | ||||||
| chr7:141089325
|
G | A | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+14633G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141089325 | ||||||
| chr7:141089490
|
G | A | 4 | a0001c0001t0003g0007a0001c0001t0005g0008a0001c0001t0025g0010others(1): Show | 4 | HG02486.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+14798G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141089490 | ||||||
| chr7:141089492
|
C | T | 4 | a0001c0001t0003g0007a0001c0001t0005g0008a0001c0001t0025g0010others(1): Show | 4 | HG02486.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+14800C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141089492 | ||||||
| chr7:141089494
|
G | GAAATA | 4 | a0001c0001t0003g0007a0001c0001t0005g0008a0001c0001t0025g0010others(1): Show | 4 | HG02486.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+14802_382+1480 others(9): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141089494 | ||||||
| chr7:141089623
|
A | G | 4 | a0001c0001t0003g0007a0001c0001t0005g0008a0001c0001t0025g0010others(1): Show | 4 | HG02486.hp1 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+14931A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141089623 | ||||||
| chr7:141089815
|
A | T | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382+15123A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141089815 | ||||||
| chr7:141089880
|
G | A | 1 | a0001c0003t0018g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.382+15188G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141089880 | ||||||
| chr7:141089910
|
A | G | 2 | a0001c0002t0006g0040a0001c0002t0026g0041 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.382+15218A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141089910 | ||||||
| chr7:141089953
|
A | G | 33 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(30): Show | 33 | HG00544.hp1 HG01243.hp1 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.382+15261A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141089953 | ||||||
| chr7:141090186
|
T | A | 2 | a0001c0002t0006g0040a0001c0002t0026g0041 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.382+15494T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141090186 | ||||||
| chr7:141090187
|
A | T | 2 | a0001c0001t0006g0017a0001c0002t0015g0056 | 2 | HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.382+15495A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141090187 | ||||||
| chr7:141090239
|
GCAATGGT others(5): Show |
G | 11 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0004g0029others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.382+15550_382+1556 others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141090239 | |||||
| chr7:141091506
|
T | A | 33 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(30): Show | 33 | HG00544.hp1 HG01243.hp1 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.382+16814T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141091506 | ||||||
| chr7:141091520
|
G | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0080a0001c0001t0002g0027others(10): Show | 13 | HG00544.hp1 HG01261.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.382+16828G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141091520 | ||||||
| chr7:141091715
|
T | C | 2 | a0001c0001t0002g0019a0001c0001t0003g0020 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.382+17023T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141091715 | ||||||
| chr7:141091846
|
A | G | 1 | a0001c0003t0001g0074 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.382+17154A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141091846 | ||||||
| chr7:141092020
|
A | G | 72 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(69): Show | 72 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(69): Show |
intron_variant | MODIFIER | c.382+17328A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141092020 | ||||||
| chr7:141092165
|
A | C | 1 | a0001c0002t0007g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.382+17473A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141092165 | ||||||
| chr7:141092330
|
G | A | 3 | a0001c0001t0002g0019a0001c0001t0003g0020a0001c0001t0023g0018 | 3 | HG03209.hp2 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.382+17638G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141092330 | ||||||
| chr7:141092593
|
C | T | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+17901C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141092593 | ||||||
| chr7:141093321
|
T | C | 34 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(31): Show | 34 | HG00544.hp1 HG01243.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.382+18629T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141093321 | ||||||
| chr7:141093420
|
A | G | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.382+18728A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141093420 | ||||||
| chr7:141093661
|
G | A | 2 | a0001c0002t0006g0040a0001c0002t0026g0041 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.382+18969G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141093661 | ||||||
| chr7:141093787
|
G | A | 11 | a0001c0001t0001g0015a0001c0001t0002g0027a0001c0001t0004g0023others(8): Show | 11 | HG01261.hp1 HG01884.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.382+19095G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141093787 | ||||||
| chr7:141094225
|
T | G | 2 | a0001c0002t0006g0040a0001c0002t0026g0041 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.382+19533T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141094225 | ||||||
| chr7:141094438
|
A | G | 2 | a0001c0002t0006g0040a0001c0002t0026g0041 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.382+19746A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141094438 | ||||||
| chr7:141094705
|
G | A | 1 | a0001c0002t0011g0044 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.382+20013G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141094705 | ||||||
| chr7:141095239
|
G | A | 2 | a0001c0002t0001g0065a0001c0002t0013g0059 | 2 | HG01255.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.382+20547G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141095239 | ||||||
| chr7:141095276
|
G | T | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.382+20584G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141095276 | ||||||
| chr7:141095498
|
A | G | 36 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(33): Show | 36 | HG00544.hp1 HG01243.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.382+20806A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141095498 | ||||||
| chr7:141095585
|
A | G | 1 | a0001c0002t0013g0059 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.382+20893A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141095585 | ||||||
| chr7:141095868
|
C | T | 1 | a0001c0001t0016g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.382+21176C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141095868 | ||||||
| chr7:141097089
|
CA | C | 20 | a0001c0001t0001g0080a0001c0001t0002g0019a0001c0001t0003g0007others(17): Show | 20 | HG00544.hp1 HG01261.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.382+22412delA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141097089 | |||||
| chr7:141097089
|
CAA | C | 10 | a0001c0001t0001g0015a0001c0001t0002g0027a0001c0001t0004g0023others(7): Show | 10 | HG01884.hp2 HG01952.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.382+22411_382+2241 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141097089 | |||||
| chr7:141097365
|
CA | C | 37 | a0001c0002t0001g0042a0001c0002t0001g0048a0001c0002t0001g0057others(34): Show | 37 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.382+22696delA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141097365 | |||||
| chr7:141097365
|
CAA | C | 6 | a0001c0001t0001g0080a0001c0001t0002g0019a0001c0001t0008g0030others(3): Show | 6 | HG00544.hp1 HG01891.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+22695_382+2269 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141097365 | |||||
| chr7:141097365
|
CAAA | C | 26 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(23): Show | 26 | HG01243.hp1 HG01261.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.382+22694_382+2269 others(7): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141097365 | |||||
| chr7:141097523
|
C | T | 2 | a0001c0002t0006g0040a0001c0002t0026g0041 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.382+22831C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141097523 | ||||||
| chr7:141097568
|
A | C | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+22876A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141097568 | ||||||
| chr7:141097642
|
A | AT | 5 | a0001c0001t0002g0019a0001c0001t0003g0020a0001c0001t0008g0004others(2): Show | 5 | HG03209.hp2 HG03471.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+22954dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141097642 | |||||
| chr7:141097730
|
T | C | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+23038T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141097730 | ||||||
| chr7:141097770
|
G | T | 36 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(33): Show | 36 | HG00544.hp1 HG01243.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.382+23078G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141097770 | ||||||
| chr7:141097793
|
C | CTT | 29 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(26): Show | 29 | HG01243.hp1 HG01261.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.382+23117_382+2311 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141097793 | |||||
| chr7:141097793
|
C | T | 1 | a0001c0001t0005g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.382+23101C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141097793 | ||||||
| chr7:141097853
|
A | C | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+23161A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141097853 | ||||||
| chr7:141097912
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+23220C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141097912 | ||||||
| chr7:141098028
|
G | A | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+23336G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141098028 | ||||||
| chr7:141098374
|
T | C | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.382+23682T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141098374 | ||||||
| chr7:141098478
|
C | T | 1 | a0001c0001t0022g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.382+23786C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141098478 | ||||||
| chr7:141098544
|
A | C | 36 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(33): Show | 36 | HG00544.hp1 HG01243.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.382+23852A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141098544 | ||||||
| chr7:141098617
|
A | T | 1 | a0001c0001t0020g0006 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.382+23925A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141098617 | ||||||
| chr7:141098681
|
T | C | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+23989T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141098681 | ||||||
| chr7:141098783
|
G | A | 35 | a0001c0002t0001g0048a0001c0002t0001g0057a0001c0002t0001g0064others(32): Show | 35 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.382+24091G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141098783 | ||||||
| chr7:141099385
|
A | AAC | 4 | a0001c0001t0009g0078a0001c0001t0021g0077a0001c0001t0035g0079others(1): Show | 4 | HG02258.hp1 HG02647.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+24695_382+2469 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141099385 | |||||
| chr7:141099467
|
A | G | 1 | a0001c0001t0016g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.382+24775A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141099467 | ||||||
| chr7:141099680
|
G | A | 36 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(33): Show | 36 | HG00544.hp1 HG01243.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.382+24988G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141099680 | ||||||
| chr7:141099707
|
G | T | 1 | a0001c0002t0016g0072 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.382+25015G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141099707 | ||||||
| chr7:141099832
|
C | CT | 60 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(57): Show | 60 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(57): Show |
intron_variant | MODIFIER | c.382+25155dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141099832 | |||||
| chr7:141099832
|
C | CTT | 7 | a0001c0001t0002g0019a0001c0001t0003g0020a0001c0001t0008g0004others(4): Show | 7 | HG03209.hp2 HG03471.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.382+25154_382+2515 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141099832 | |||||
| chr7:141099998
|
G | GT | 2 | a0001c0002t0001g0048a0001c0003t0018g0046 | 2 | HG01256.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.382+25308dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141099998 | |||||
| chr7:141100098
|
C | T | 1 | a0001c0002t0032g0071 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.382+25406C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141100098 | ||||||
| chr7:141100462
|
A | G | 2 | a0001c0001t0001g0080a0001c0001t0028g0022 | 2 | HG00544.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.382+25770A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141100462 | ||||||
| chr7:141100616
|
G | A | 40 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(37): Show | 40 | HG00544.hp1 HG01106.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.382+25924G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141100616 | ||||||
| chr7:141100771
|
A | T | 1 | a0001c0002t0037g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.382+26079A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141100771 | ||||||
| chr7:141100836
|
C | T | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+26144C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141100836 | ||||||
| chr7:141100890
|
A | C | 15 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0004g0029others(12): Show | 15 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.382+26198A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141100890 | ||||||
| chr7:141101165
|
G | A | 1 | a0001c0005t0001g0005 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.382+26473G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141101165 | ||||||
| chr7:141101629
|
G | A | 35 | a0001c0002t0001g0048a0001c0002t0001g0057a0001c0002t0001g0064others(32): Show | 35 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.382+26937G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141101629 | ||||||
| chr7:141101657
|
T | A | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382+26965T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141101657 | ||||||
| chr7:141101908
|
C | CGT | 9 | a0001c0001t0003g0020a0001c0001t0025g0010a0001c0002t0001g0065others(6): Show | 9 | HG00544.hp2 HG01255.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.382+27249_382+2725 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141101908 | |||||
| chr7:141101908
|
C | CGTGT | 5 | a0001c0001t0022g0013a0001c0001t0044g0001a0001c0002t0001g0042others(2): Show | 5 | HG01261.hp1 HG02027.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.382+27247_382+2725 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141101908 | |||||
| chr7:141101908
|
CGT | C | 2 | a0001c0001t0005g0014a0001c0001t0008g0004 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.382+27249_382+2725 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141101908 | |||||
| chr7:141101908
|
CGTGT | C | 15 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(12): Show | 15 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.382+27247_382+2725 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141101908 | |||||
| chr7:141101908
|
CGTGTGT | C | 6 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0006g0025others(3): Show | 6 | HG01884.hp2 HG01952.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+27245_382+2725 others(10): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141101908 | |||||
| chr7:141102292
|
A | G | 1 | a0001c0002t0042g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.382+27600A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141102292 | ||||||
| chr7:141102314
|
A | C | 2 | a0001c0002t0006g0040a0001c0002t0026g0041 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.382+27622A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141102314 | ||||||
| chr7:141103245
|
A | G | 1 | a0001c0001t0028g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.382+28553A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141103245 | ||||||
| chr7:141103286
|
T | A | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.382+28594T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141103286 | ||||||
| chr7:141103690
|
A | C | 3 | a0001c0001t0002g0019a0001c0001t0003g0020a0001c0001t0023g0018 | 3 | HG03209.hp2 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.382+28998A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141103690 | ||||||
| chr7:141103720
|
A | G | 38 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(35): Show | 38 | HG00544.hp1 HG01106.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.382+29028A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141103720 | ||||||
| chr7:141103722
|
A | G | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382+29030A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141103722 | ||||||
| chr7:141103753
|
A | G | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.382+29061A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141103753 | ||||||
| chr7:141105005
|
C | G | 35 | a0001c0002t0001g0048a0001c0002t0001g0057a0001c0002t0001g0064others(32): Show | 35 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.382+30313C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141105005 | ||||||
| chr7:141105091
|
A | T | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+30399A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141105091 | ||||||
| chr7:141105368
|
G | A | 3 | a0001c0002t0008g0003a0001c0002t0024g0002a0001c0002t0030g0067 | 3 | HG02109.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.382+30676G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141105368 | ||||||
| chr7:141105461
|
C | T | 2 | a0001c0002t0006g0040a0001c0002t0026g0041 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.382+30769C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141105461 | ||||||
| chr7:141105849
|
G | C | 40 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(37): Show | 40 | HG00544.hp1 HG01106.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.382+31157G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141105849 | ||||||
| chr7:141106085
|
C | CA | 61 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(58): Show | 61 | HG00544.hp1 HG00544.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.382+31409dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141106085 | |||||
| chr7:141106085
|
C | CAA | 10 | a0001c0001t0020g0006a0001c0002t0001g0057a0001c0002t0005g0049others(7): Show | 10 | HG01106.hp1 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.382+31408_382+3140 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141106085 | |||||
| chr7:141106172
|
G | C | 76 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(73): Show | 76 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(73): Show |
intron_variant | MODIFIER | c.382+31480G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141106172 | ||||||
| chr7:141106287
|
G | A | 2 | a0001c0002t0006g0040a0001c0002t0026g0041 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.382+31595G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141106287 | ||||||
| chr7:141106733
|
A | G | 1 | a0001c0002t0006g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.382+32041A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141106733 | ||||||
| chr7:141106742
|
A | G | 3 | a0001c0001t0002g0019a0001c0001t0003g0020a0001c0001t0023g0018 | 3 | HG03209.hp2 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.382+32050A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141106742 | ||||||
| chr7:141106845
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.382+32153C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141106845 | ||||||
| chr7:141107220
|
A | C | 2 | a0001c0002t0006g0040a0001c0002t0026g0041 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.382+32528A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141107220 | ||||||
| chr7:141107436
|
G | A | 12 | a0001c0001t0001g0012a0001c0001t0002g0019a0001c0001t0003g0020others(9): Show | 12 | HG01106.hp2 HG02258.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.382+32744G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141107436 | ||||||
| chr7:141107946
|
G | A | 1 | a0001c0002t0031g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.382+33254G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141107946 | ||||||
| chr7:141107978
|
G | C | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+33286G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141107978 | ||||||
| chr7:141108256
|
A | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0080a0001c0001t0002g0027others(10): Show | 13 | HG00544.hp1 HG01261.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.382+33564A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141108256 | ||||||
| chr7:141108419
|
A | T | 1 | a0001c0001t0029g0026 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.382+33727A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141108419 | ||||||
| chr7:141108847
|
A | G | 3 | a0001c0002t0012g0045a0001c0003t0001g0068a0001c0003t0018g0046 | 3 | HG01243.hp2 HG01256.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.382+34155A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141108847 | ||||||
| chr7:141108954
|
T | A | 1 | a0001c0002t0001g0048 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.382+34262T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141108954 | ||||||
| chr7:141109068
|
G | A | 15 | a0001c0001t0001g0035a0001c0001t0004g0029a0001c0001t0014g0033others(12): Show | 15 | HG01243.hp1 HG01884.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.382+34376G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141109068 | ||||||
| chr7:141109232
|
G | A | 1 | a0001c0001t0020g0006 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.382+34540G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141109232 | ||||||
| chr7:141109405
|
T | C | 26 | a0001c0001t0001g0012a0001c0001t0002g0019a0001c0001t0003g0007others(23): Show | 26 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.382+34713T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141109405 | ||||||
| chr7:141109416
|
A | C | 1 | a0001c0001t0004g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.382+34724A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141109416 | ||||||
| chr7:141109717
|
T | A | 4 | a0001c0002t0001g0076a0001c0002t0008g0003a0001c0002t0024g0002others(1): Show | 4 | HG03225.hp1 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+35025T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141109717 | ||||||
| chr7:141109924
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016 | 3 | HG02258.hp2 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.382+35232G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141109924 | ||||||
| chr7:141110499
|
T | C | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+35807T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141110499 | ||||||
| chr7:141110717
|
G | A | 2 | a0001c0001t0010g0021a0001c0004t0043g0032 | 2 | HG02109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.382+36025G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141110717 | ||||||
| chr7:141110849
|
A | G | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382+36157A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141110849 | ||||||
| chr7:141110870
|
G | A | 28 | a0001c0001t0001g0012a0001c0001t0002g0019a0001c0001t0003g0007others(25): Show | 28 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.382+36178G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141110870 | ||||||
| chr7:141110889
|
G | A | 1 | a0001c0001t0004g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.382+36197G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141110889 | ||||||
| chr7:141111001
|
G | C | 1 | a0001c0001t0014g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.382+36309G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141111001 | ||||||
| chr7:141111092
|
C | T | 4 | a0001c0001t0001g0080a0001c0002t0037g0075a0001c0003t0001g0055others(1): Show | 4 | HG00544.hp1 HG01256.hp1 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+36400C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141111092 | ||||||
| chr7:141111145
|
T | A | 1 | a0001c0001t0016g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.382+36453T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141111145 | ||||||
| chr7:141111445
|
T | A | 25 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(22): Show | 25 | HG00544.hp1 HG01256.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.382+36753T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141111445 | ||||||
| chr7:141112119
|
A | G | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.382+37427A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141112119 | ||||||
| chr7:141112412
|
C | A | 3 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016 | 3 | HG02258.hp2 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.382+37720C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141112412 | ||||||
| chr7:141112494
|
T | C | 5 | a0001c0001t0012g0036a0001c0002t0001g0048a0001c0002t0001g0065others(2): Show | 5 | HG01255.hp2 HG01952.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.382+37802T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141112494 | ||||||
| chr7:141112511
|
C | T | 1 | a0001c0001t0006g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.382+37819C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141112511 | ||||||
| chr7:141113139
|
T | C | 31 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0002g0019others(28): Show | 31 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.382+38447T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141113139 | ||||||
| chr7:141113217
|
G | A | 12 | a0001c0002t0001g0057a0001c0002t0002g0043a0001c0002t0007g0053others(9): Show | 12 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.382+38525G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141113217 | ||||||
| chr7:141113245
|
G | A | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382+38553G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141113245 | ||||||
| chr7:141113257
|
C | T | 12 | a0001c0002t0001g0057a0001c0002t0002g0043a0001c0002t0007g0053others(9): Show | 12 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.382+38565C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141113257 | ||||||
| chr7:141113672
|
A | C | 7 | a0001c0001t0001g0038a0001c0001t0005g0014a0001c0001t0016g0037others(4): Show | 7 | HG01891.hp1 HG02083.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.382+38980A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141113672 | ||||||
| chr7:141113901
|
G | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.382+39209G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141113901 | ||||||
| chr7:141113961
|
A | G | 7 | a0001c0001t0001g0012a0001c0001t0007g0011a0001c0001t0008g0030others(4): Show | 7 | HG01106.hp2 HG02647.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.382+39269A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141113961 | ||||||
| chr7:141114221
|
T | G | 3 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016 | 3 | HG02258.hp2 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.382+39529T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141114221 | ||||||
| chr7:141114320
|
CTCTCCCT others(14): Show |
C | 1 | a0001c0001t0004g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.382+39714_382+3973 others(25): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141114320 | |||||
| chr7:141114388
|
C | T | 1 | a0001c0002t0006g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.382+39696C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141114388 | ||||||
| chr7:141114499
|
T | C | 59 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(56): Show | 59 | HG00544.hp1 HG01106.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.382+39807T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141114499 | ||||||
| chr7:141114607
|
G | A | 2 | a0001c0002t0007g0053a0001c0003t0019g0070 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.382+39915G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141114607 | ||||||
| chr7:141114850
|
T | C | 1 | a0001c0002t0001g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.382+40158T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141114850 | ||||||
| chr7:141115002
|
G | A | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+40310G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141115002 | ||||||
| chr7:141115013
|
G | T | 4 | a0001c0001t0023g0018a0001c0001t0044g0001a0001c0002t0001g0042others(1): Show | 4 | HG02572.hp1 HG03453.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+40321G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141115013 | ||||||
| chr7:141115035
|
T | TTG | 4 | a0001c0001t0015g0028a0001c0001t0029g0026a0001c0001t0035g0079others(1): Show | 4 | HG01884.hp2 HG01978.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+40365_382+4036 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141115035 | |||||
| chr7:141115104
|
G | A | 1 | a0001c0001t0004g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.382+40412G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141115104 | ||||||
| chr7:141115107
|
A | C | 1 | a0001c0001t0004g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.382+40415A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141115107 | ||||||
| chr7:141115159
|
C | T | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+40467C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141115159 | ||||||
| chr7:141115282
|
T | TCA | 25 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0003g0007others(22): Show | 25 | HG02027.hp1 HG02083.hp1 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.382+40592_382+4059 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141115282 | |||||
| chr7:141115647
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+40955G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141115647 | ||||||
| chr7:141116040
|
C | T | 27 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(24): Show | 27 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.382+41348C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141116040 | ||||||
| chr7:141116054
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016 | 3 | HG02258.hp2 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.382+41362G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141116054 | ||||||
| chr7:141116066
|
A | G | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382+41374A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141116066 | ||||||
| chr7:141116079
|
G | A | 37 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(34): Show | 37 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.382+41387G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141116079 | ||||||
| chr7:141116130
|
C | T | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.382+41438C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141116130 | ||||||
| chr7:141116794
|
G | T | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+42102G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141116794 | ||||||
| chr7:141116964
|
C | T | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382+42272C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141116964 | ||||||
| chr7:141117343
|
C | T | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+42651C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141117343 | ||||||
| chr7:141117513
|
T | C | 11 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0006g0017others(8): Show | 11 | HG01106.hp2 HG01255.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+42821T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141117513 | ||||||
| chr7:141117704
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0007g0011a0001c0005t0001g0005 | 3 | HG01106.hp2 HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.382+43012G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141117704 | ||||||
| chr7:141117867
|
G | A | 40 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(37): Show | 40 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.382+43175G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141117867 | ||||||
| chr7:141117984
|
A | G | 31 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(28): Show | 31 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.382+43292A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141117984 | ||||||
| chr7:141118049
|
T | C | 31 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(28): Show | 31 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.382+43357T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141118049 | ||||||
| chr7:141118444
|
A | C | 6 | a0001c0001t0008g0030a0001c0001t0010g0021a0001c0001t0014g0039others(3): Show | 6 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+43752A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141118444 | ||||||
| chr7:141118480
|
T | C | 1 | a0001c0002t0006g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.382+43788T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141118480 | ||||||
| chr7:141118612
|
C | T | 28 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(25): Show | 28 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.382+43920C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141118612 | ||||||
| chr7:141118977
|
C | T | 6 | a0001c0001t0008g0030a0001c0001t0010g0021a0001c0001t0016g0037others(3): Show | 6 | HG01891.hp1 HG02647.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+44285C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141118977 | ||||||
| chr7:141119080
|
A | G | 3 | a0001c0001t0001g0038a0001c0002t0011g0044a0001c0002t0031g0063 | 3 | HG02083.hp1 HG02602.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.382+44388A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141119080 | ||||||
| chr7:141119753
|
A | G | 38 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(35): Show | 38 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.382+45061A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141119753 | ||||||
| chr7:141119975
|
G | A | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.382+45283G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141119975 | ||||||
| chr7:141120135
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.382+45443C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141120135 | ||||||
| chr7:141120656
|
T | C | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+45964T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141120656 | ||||||
| chr7:141120799
|
T | TA | 5 | a0001c0001t0002g0019a0001c0001t0004g0029a0001c0001t0023g0018others(2): Show | 5 | HG02572.hp1 HG02630.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.382+46112dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141120799 | |||||
| chr7:141120804
|
AT | A | 6 | a0001c0001t0001g0038a0001c0001t0005g0014a0001c0002t0011g0044others(3): Show | 6 | HG02083.hp1 HG02602.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+46113delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141120804 | ||||||
| chr7:141120805
|
T | A | 32 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0002g0019others(29): Show | 32 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.382+46113T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141120805 | ||||||
| chr7:141120950
|
G | A | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+46258G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141120950 | ||||||
| chr7:141120979
|
A | T | 3 | a0001c0001t0003g0007a0001c0002t0002g0043a0001c0002t0041g0058 | 3 | HG02027.hp1 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.382+46287A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141120979 | ||||||
| chr7:141121064
|
T | C | 1 | a0001c0001t0004g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.382+46372T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141121064 | ||||||
| chr7:141121195
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+46503A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141121195 | ||||||
| chr7:141121246
|
G | A | 1 | a0001c0001t0012g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.382+46554G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141121246 | ||||||
| chr7:141121451
|
C | T | 2 | a0001c0001t0008g0004a0001c0004t0043g0032 | 2 | HG02109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.382+46759C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141121451 | ||||||
| chr7:141121752
|
A | G | 1 | a0001c0001t0020g0006 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.382+47060A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141121752 | ||||||
| chr7:141121787
|
A | G | 1 | a0001c0003t0001g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.382+47095A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141121787 | ||||||
| chr7:141121820
|
G | A | 4 | a0001c0001t0005g0008a0001c0001t0025g0010a0001c0001t0034g0009others(1): Show | 4 | HG02486.hp1 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+47128G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141121820 | ||||||
| chr7:141121839
|
C | G | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.382+47147C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141121839 | ||||||
| chr7:141121844
|
C | A | 4 | a0001c0001t0002g0019a0001c0001t0008g0004a0001c0001t0008g0030others(1): Show | 4 | HG02109.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+47152C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141121844 | ||||||
| chr7:141122371
|
A | G | 38 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(35): Show | 38 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(35): Show |
intron_variant | MODIFIER | c.382+47679A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141122371 | ||||||
| chr7:141122630
|
G | A | 1 | a0001c0002t0006g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.382+47938G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141122630 | ||||||
| chr7:141122631
|
G | A | 4 | a0001c0001t0012g0036a0001c0002t0001g0048a0001c0002t0001g0065others(1): Show | 4 | HG01255.hp2 HG01952.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+47939G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141122631 | ||||||
| chr7:141123021
|
G | C | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+48329G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141123021 | ||||||
| chr7:141123318
|
G | A | 40 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(37): Show | 40 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.382+48626G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141123318 | ||||||
| chr7:141123392
|
G | A | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+48700G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141123392 | ||||||
| chr7:141123785
|
A | C | 4 | a0001c0001t0002g0019a0001c0001t0008g0004a0001c0002t0026g0041others(1): Show | 4 | HG02109.hp2 HG02572.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+49093A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141123785 | ||||||
| chr7:141123842
|
T | G | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+49150T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141123842 | ||||||
| chr7:141123880
|
G | GTAGC | 7 | a0001c0001t0008g0030a0001c0001t0010g0021a0001c0001t0014g0039others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.382+49190_382+4919 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141123880 | |||||
| chr7:141124135
|
G | C | 3 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0002t0010g0066 | 3 | HG01891.hp1 HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.382+49443G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141124135 | ||||||
| chr7:141124186
|
G | A | 2 | a0001c0002t0003g0052a0001c0002t0017g0062 | 2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.382+49494G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141124186 | ||||||
| chr7:141124366
|
A | T | 1 | a0001c0002t0001g0057 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.382+49674A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141124366 | ||||||
| chr7:141124524
|
G | A | 1 | a0001c0002t0010g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.382+49832G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141124524 | ||||||
| chr7:141125398
|
C | A | 1 | a0001c0002t0013g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.382+50706C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141125398 | ||||||
| chr7:141125402
|
G | A | 7 | a0001c0001t0008g0030a0001c0001t0010g0021a0001c0001t0014g0039others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.382+50710G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141125402 | ||||||
| chr7:141125404
|
C | T | 18 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0005g0008others(15): Show | 18 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.382+50712C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141125404 | ||||||
| chr7:141125441
|
G | A | 6 | a0001c0001t0002g0027a0001c0001t0006g0025a0001c0001t0015g0028others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+50749G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141125441 | ||||||
| chr7:141125457
|
T | C | 31 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0002g0019others(28): Show | 31 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.382+50765T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141125457 | ||||||
| chr7:141125537
|
C | T | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+50845C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141125537 | ||||||
| chr7:141125578
|
G | A | 1 | a0001c0002t0036g0069 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.382+50886G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141125578 | ||||||
| chr7:141125680
|
GA | G | 4 | a0001c0002t0001g0076a0001c0002t0008g0003a0001c0002t0024g0002others(1): Show | 4 | HG03579.hp1 NA18522.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+51005delA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141125680 | |||||
| chr7:141125753
|
C | T | 6 | a0001c0001t0008g0030a0001c0001t0010g0021a0001c0001t0014g0039others(3): Show | 6 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+51061C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141125753 | ||||||
| chr7:141125840
|
T | C | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+51148T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141125840 | ||||||
| chr7:141126019
|
C | T | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382+51327C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141126019 | ||||||
| chr7:141126123
|
C | T | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382+51431C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141126123 | ||||||
| chr7:141126162
|
G | GAAGA | 18 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0005g0008others(15): Show | 18 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.382+51471_382+5147 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141126162 | |||||
| chr7:141126385
|
C | T | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+51693C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141126385 | ||||||
| chr7:141126632
|
T | G | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+51940T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141126632 | ||||||
| chr7:141126729
|
C | T | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+52037C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141126729 | ||||||
| chr7:141126789
|
G | A | 1 | a0001c0002t0041g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.382+52097G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141126789 | ||||||
| chr7:141126856
|
A | AGT | 6 | a0001c0002t0001g0064a0001c0002t0001g0076a0001c0002t0008g0003others(3): Show | 6 | HG02486.hp2 HG03540.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+52199_382+5220 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141126856 | |||||
| chr7:141126856
|
AGT | A | 14 | a0001c0001t0002g0019a0001c0001t0003g0007a0001c0001t0005g0014others(11): Show | 14 | HG01891.hp2 HG02027.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.382+52199_382+5220 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141126856 | |||||
| chr7:141126856
|
AGTGT | A | 7 | a0001c0001t0008g0030a0001c0001t0016g0037a0001c0001t0020g0006others(4): Show | 7 | HG01891.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.382+52197_382+5220 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141126856 | |||||
| chr7:141126856
|
AGTGTGT | A | 18 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0005g0008others(15): Show | 18 | HG01106.hp2 HG01243.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.382+52195_382+5220 others(10): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141126856 | |||||
| chr7:141126889
|
G | C | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382+52197G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141126889 | ||||||
| chr7:141127253
|
T | A | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+52561T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141127253 | ||||||
| chr7:141127459
|
A | G | 5 | a0001c0001t0002g0019a0001c0001t0023g0018a0001c0002t0006g0040others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.382+52767A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141127459 | ||||||
| chr7:141127595
|
G | C | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382+52903G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141127595 | ||||||
| chr7:141127793
|
G | A | 15 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0005g0008others(12): Show | 15 | HG01106.hp2 HG01255.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.382+53101G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141127793 | ||||||
| chr7:141128027
|
G | A | 5 | a0001c0001t0002g0019a0001c0001t0023g0018a0001c0002t0006g0040others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.382+53335G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141128027 | ||||||
| chr7:141128118
|
T | C | 5 | a0001c0001t0002g0019a0001c0001t0023g0018a0001c0002t0006g0040others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.382+53426T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141128118 | ||||||
| chr7:141128344
|
T | C | 15 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0005g0008others(12): Show | 15 | HG01106.hp2 HG01255.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.382+53652T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141128344 | ||||||
| chr7:141128350
|
A | G | 5 | a0001c0001t0002g0019a0001c0001t0023g0018a0001c0002t0006g0040others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.382+53658A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141128350 | ||||||
| chr7:141128418
|
A | G | 2 | a0001c0001t0022g0013a0002c0006t0039g0061 | 2 | HG01261.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.382+53726A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141128418 | ||||||
| chr7:141128554
|
C | G | 8 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0004g0029others(5): Show | 8 | HG01884.hp2 HG01952.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.382+53862C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141128554 | ||||||
| chr7:141128838
|
G | T | 1 | a0001c0002t0006g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.382+54146G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141128838 | ||||||
| chr7:141128973
|
G | A | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.382+54281G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141128973 | ||||||
| chr7:141129084
|
T | C | 6 | a0001c0001t0002g0019a0001c0001t0008g0004a0001c0001t0023g0018others(3): Show | 6 | HG02109.hp2 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+54392T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141129084 | ||||||
| chr7:141129142
|
T | C | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+54450T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141129142 | ||||||
| chr7:141129152
|
A | T | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.382+54460A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141129152 | ||||||
| chr7:141129235
|
A | T | 2 | a0001c0002t0003g0052a0001c0002t0017g0062 | 2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.382+54543A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141129235 | ||||||
| chr7:141129302
|
G | A | 3 | a0001c0001t0023g0018a0001c0002t0006g0040a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.382+54610G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141129302 | ||||||
| chr7:141129415
|
A | T | 1 | a0001c0001t0014g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.382+54723A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141129415 | ||||||
| chr7:141129417
|
C | T | 1 | a0001c0001t0014g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.382+54725C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141129417 | ||||||
| chr7:141129743
|
G | A | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.382+55051G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141129743 | ||||||
| chr7:141129862
|
A | G | 3 | a0001c0001t0023g0018a0001c0002t0006g0040a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.382+55170A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141129862 | ||||||
| chr7:141129897
|
A | G | 2 | a0001c0001t0002g0019a0001c0004t0043g0032 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.382+55205A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141129897 | ||||||
| chr7:141130049
|
T | A | 2 | a0001c0001t0023g0018a0001c0002t0006g0040 | 2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.382+55357T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141130049 | ||||||
| chr7:141130069
|
G | A | 3 | a0001c0001t0023g0018a0001c0002t0006g0040a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.382+55377G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141130069 | ||||||
| chr7:141130131
|
A | G | 2 | a0001c0001t0002g0019a0001c0004t0043g0032 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.382+55439A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141130131 | ||||||
| chr7:141130330
|
C | T | 3 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0002t0010g0066 | 3 | HG01891.hp1 HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.382+55638C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141130330 | ||||||
| chr7:141130684
|
A | T | 1 | a0001c0003t0019g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.382+55992A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141130684 | ||||||
| chr7:141130776
|
T | C | 3 | a0001c0001t0023g0018a0001c0002t0006g0040a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.382+56084T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141130776 | ||||||
| chr7:141130862
|
A | G | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.382+56170A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141130862 | ||||||
| chr7:141131003
|
G | A | 1 | a0001c0002t0006g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.382+56311G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141131003 | ||||||
| chr7:141131079
|
C | A | 7 | a0001c0001t0008g0030a0001c0001t0010g0021a0001c0001t0014g0039others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.382+56387C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141131079 | ||||||
| chr7:141131352
|
A | G | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382+56660A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141131352 | ||||||
| chr7:141131504
|
C | A | 7 | a0001c0001t0008g0030a0001c0001t0010g0021a0001c0001t0014g0039others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.382+56812C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141131504 | ||||||
| chr7:141131541
|
C | A | 80 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(77): Show | 80 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.382+56849C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141131541 | ||||||
| chr7:141131659
|
C | T | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+56967C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141131659 | ||||||
| chr7:141131660
|
T | C | 1 | a0001c0002t0012g0045 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.382+56968T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141131660 | ||||||
| chr7:141131715
|
G | C | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+57023G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141131715 | ||||||
| chr7:141131900
|
C | T | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.382+57208C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141131900 | ||||||
| chr7:141132300
|
T | A | 2 | a0001c0001t0023g0018a0001c0002t0006g0040 | 2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.382+57608T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141132300 | ||||||
| chr7:141132349
|
T | C | 2 | a0001c0001t0023g0018a0001c0002t0006g0040 | 2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.382+57657T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141132349 | ||||||
| chr7:141132390
|
A | C | 2 | a0001c0001t0023g0018a0001c0002t0006g0040 | 2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.382+57698A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141132390 | ||||||
| chr7:141132524
|
A | G | 79 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(76): Show | 79 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(76): Show |
intron_variant | MODIFIER | c.382+57832A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141132524 | ||||||
| chr7:141132737
|
A | T | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.382+58045A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141132737 | ||||||
| chr7:141132761
|
C | T | 2 | a0001c0001t0023g0018a0001c0002t0006g0040 | 2 | HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.382+58069C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141132761 | ||||||
| chr7:141132799
|
A | G | 1 | a0001c0002t0006g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.382+58107A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141132799 | ||||||
| chr7:141133521
|
T | C | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382+58829T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141133521 | ||||||
| chr7:141133554
|
A | G | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+58862A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141133554 | ||||||
| chr7:141133859
|
C | G | 3 | a0001c0001t0023g0018a0001c0002t0006g0040a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.382+59167C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141133859 | ||||||
| chr7:141134043
|
A | C | 3 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0002t0010g0066 | 3 | HG01891.hp1 HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.382+59351A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141134043 | ||||||
| chr7:141134304
|
A | G | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+59612A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141134304 | ||||||
| chr7:141134368
|
G | A | 3 | a0001c0001t0023g0018a0001c0002t0006g0040a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.382+59676G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141134368 | ||||||
| chr7:141134474
|
A | G | 1 | a0001c0002t0007g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.382+59782A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141134474 | ||||||
| chr7:141134659
|
C | A | 15 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0005g0008others(12): Show | 15 | HG01106.hp2 HG01255.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.382+59967C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141134659 | ||||||
| chr7:141134884
|
A | G | 1 | a0001c0002t0006g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.382+60192A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141134884 | ||||||
| chr7:141135446
|
A | G | 6 | a0001c0001t0002g0019a0001c0001t0008g0004a0001c0001t0023g0018others(3): Show | 6 | HG02109.hp2 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+60754A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141135446 | ||||||
| chr7:141135454
|
T | C | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.382+60762T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141135454 | ||||||
| chr7:141135473
|
T | C | 7 | a0001c0001t0008g0030a0001c0001t0010g0021a0001c0001t0014g0039others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.382+60781T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141135473 | ||||||
| chr7:141135921
|
G | GT | 4 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0002t0001g0042others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+61237dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141135921 | |||||
| chr7:141136055
|
G | A | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+61363G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141136055 | ||||||
| chr7:141136071
|
A | G | 6 | a0001c0001t0002g0019a0001c0001t0008g0004a0001c0001t0023g0018others(3): Show | 6 | HG02109.hp2 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+61379A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141136071 | ||||||
| chr7:141136128
|
T | C | 1 | a0001c0002t0001g0048 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.382+61436T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141136128 | ||||||
| chr7:141136159
|
G | A | 12 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(9): Show | 12 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.382+61467G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141136159 | ||||||
| chr7:141136517
|
C | T | 5 | a0001c0001t0002g0019a0001c0001t0008g0004a0001c0001t0023g0018others(2): Show | 5 | HG02109.hp2 HG02630.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+61825C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141136517 | ||||||
| chr7:141136984
|
A | C | 57 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(54): Show | 57 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.382+62292A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141136984 | ||||||
| chr7:141137198
|
A | G | 4 | a0001c0001t0002g0019a0001c0001t0023g0018a0001c0002t0006g0040others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+62506A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141137198 | ||||||
| chr7:141137337
|
T | C | 8 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0010g0021others(5): Show | 8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.382+62645T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141137337 | ||||||
| chr7:141137347
|
G | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.382+62655G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141137347 | ||||||
| chr7:141137393
|
G | T | 1 | a0001c0001t0001g0038 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.382+62701G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141137393 | ||||||
| chr7:141137824
|
C | T | 64 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(61): Show | 64 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(61): Show |
intron_variant | MODIFIER | c.382+63132C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141137824 | ||||||
| chr7:141137933
|
C | T | 1 | a0001c0002t0037g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.382+63241C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141137933 | ||||||
| chr7:141138063
|
A | ATT | 10 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0010g0021others(7): Show | 10 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.382+63386_382+6338 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141138063 | |||||
| chr7:141138587
|
A | G | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+63895A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141138587 | ||||||
| chr7:141138708
|
C | A | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+64016C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141138708 | ||||||
| chr7:141138753
|
C | T | 8 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(5): Show | 8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.382+64061C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141138753 | ||||||
| chr7:141138994
|
A | G | 10 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.382+64302A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141138994 | ||||||
| chr7:141138995
|
G | A | 10 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.382+64303G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141138995 | ||||||
| chr7:141139176
|
G | T | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+64484G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141139176 | ||||||
| chr7:141139386
|
GTT | G | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+64697_382+6469 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141139386 | |||||
| chr7:141139505
|
C | A | 5 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0021g0077others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.382+64813C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141139505 | ||||||
| chr7:141139605
|
G | A | 5 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0021g0077others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.382+64913G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141139605 | ||||||
| chr7:141139766
|
GT | G | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+65088delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141139766 | |||||
| chr7:141139844
|
C | A | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+65152C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141139844 | ||||||
| chr7:141140021
|
C | T | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.382+65329C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141140021 | ||||||
| chr7:141140027
|
G | A | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+65335G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141140027 | ||||||
| chr7:141140071
|
T | C | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+65379T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141140071 | ||||||
| chr7:141140111
|
C | T | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+65419C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141140111 | ||||||
| chr7:141140254
|
C | T | 1 | a0001c0002t0013g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.382+65562C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141140254 | ||||||
| chr7:141140284
|
C | G | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+65592C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141140284 | ||||||
| chr7:141140507
|
G | C | 8 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(5): Show | 8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.382+65815G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141140507 | ||||||
| chr7:141140712
|
C | T | 8 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(5): Show | 8 | HG01891.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.382+66020C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141140712 | ||||||
| chr7:141141284
|
A | AT | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+66602dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141141284 | |||||
| chr7:141141536
|
A | G | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+66844A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141141536 | ||||||
| chr7:141141566
|
C | T | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+66874C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141141566 | ||||||
| chr7:141141865
|
T | G | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+67173T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141141865 | ||||||
| chr7:141141909
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.382+67217C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141141909 | ||||||
| chr7:141142050
|
C | T | 10 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.382+67358C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142050 | ||||||
| chr7:141142146
|
AGT | A | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+67457_382+6745 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141142146 | |||||
| chr7:141142149
|
G | C | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+67457G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142149 | ||||||
| chr7:141142153
|
G | C | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+67461G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142153 | ||||||
| chr7:141142154
|
G | A | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+67462G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142154 | ||||||
| chr7:141142155
|
T | G | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+67463T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142155 | ||||||
| chr7:141142187
|
A | G | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382+67495A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142187 | ||||||
| chr7:141142270
|
T | TACCACAT others(27): Show |
11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+67579_382+6761 others(38): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141142270 | |||||
| chr7:141142308
|
T | C | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+67616T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142308 | ||||||
| chr7:141142315
|
T | C | 6 | a0001c0001t0001g0038a0001c0001t0005g0014a0001c0002t0011g0044others(3): Show | 6 | HG02083.hp1 HG02602.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+67623T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142315 | ||||||
| chr7:141142342
|
G | T | 3 | a0001c0001t0001g0035a0001c0001t0038g0034a0001c0002t0030g0067 | 3 | HG02109.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.382+67650G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142342 | ||||||
| chr7:141142360
|
A | G | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+67668A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142360 | ||||||
| chr7:141142430
|
T | C | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+67738T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142430 | ||||||
| chr7:141142447
|
A | G | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+67755A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142447 | ||||||
| chr7:141142520
|
A | G | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+67828A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142520 | ||||||
| chr7:141142654
|
G | A | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+67962G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142654 | ||||||
| chr7:141142734
|
T | A | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+68042T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142734 | ||||||
| chr7:141142735
|
C | G | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+68043C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142735 | ||||||
| chr7:141142856
|
T | C | 79 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(76): Show | 79 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(76): Show |
intron_variant | MODIFIER | c.382+68164T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142856 | ||||||
| chr7:141142906
|
G | A | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+68214G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142906 | ||||||
| chr7:141142924
|
G | T | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.382+68232G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141142924 | ||||||
| chr7:141143113
|
C | T | 1 | a0001c0001t0014g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.382+68421C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141143113 | ||||||
| chr7:141143150
|
A | T | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382+68458A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141143150 | ||||||
| chr7:141143235
|
G | T | 1 | a0001c0001t0012g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.382+68543G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141143235 | ||||||
| chr7:141143296
|
A | G | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+68604A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141143296 | ||||||
| chr7:141143574
|
G | A | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.382+68882G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141143574 | ||||||
| chr7:141143761
|
T | C | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-68830T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141143761 | ||||||
| chr7:141143799
|
C | CT | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-68789dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141143799 | |||||
| chr7:141143889
|
A | C | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-68702A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141143889 | ||||||
| chr7:141144107
|
C | T | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-68484C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141144107 | ||||||
| chr7:141144279
|
G | A | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383-68312G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141144279 | ||||||
| chr7:141144877
|
T | A | 9 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.383-67714T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141144877 | ||||||
| chr7:141145012
|
T | C | 3 | a0001c0001t0014g0033a0001c0001t0028g0022a0001c0002t0005g0049 | 3 | HG01243.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.383-67579T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141145012 | ||||||
| chr7:141145221
|
G | A | 1 | a0001c0002t0001g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.383-67370G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141145221 | ||||||
| chr7:141145286
|
C | G | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-67305C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141145286 | ||||||
| chr7:141145356
|
G | C | 2 | a0001c0001t0023g0018a0001c0004t0043g0032 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.383-67235G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141145356 | ||||||
| chr7:141145546
|
C | T | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383-67045C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141145546 | ||||||
| chr7:141145701
|
G | C | 9 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.383-66890G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141145701 | ||||||
| chr7:141145922
|
G | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-66669G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141145922 | ||||||
| chr7:141146061
|
C | A | 2 | a0001c0001t0023g0018a0001c0004t0043g0032 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.383-66530C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141146061 | ||||||
| chr7:141146430
|
T | C | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-66161T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141146430 | ||||||
| chr7:141146486
|
T | G | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-66105T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141146486 | ||||||
| chr7:141146663
|
C | T | 1 | a0001c0002t0016g0072 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.383-65928C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141146663 | ||||||
| chr7:141147220
|
CCTCCTTC others(5): Show |
C | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.383-65348_383-6533 others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141147220 | |||||
| chr7:141147566
|
G | A | 1 | a0001c0001t0007g0011 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.383-65025G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141147566 | ||||||
| chr7:141148284
|
T | C | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-64307T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141148284 | ||||||
| chr7:141148414
|
A | G | 2 | a0001c0001t0023g0018a0001c0004t0043g0032 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.383-64177A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141148414 | ||||||
| chr7:141148531
|
A | G | 10 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.383-64060A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141148531 | ||||||
| chr7:141148980
|
A | G | 10 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(7): Show | 10 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.383-63611A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141148980 | ||||||
| chr7:141149114
|
G | A | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-63477G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141149114 | ||||||
| chr7:141149194
|
A | T | 2 | a0001c0001t0023g0018a0001c0004t0043g0032 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.383-63397A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141149194 | ||||||
| chr7:141149271
|
T | C | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-63320T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141149271 | ||||||
| chr7:141149472
|
C | G | 1 | a0002c0006t0039g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.383-63119C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141149472 | ||||||
| chr7:141149478
|
G | A | 1 | a0001c0003t0001g0068 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.383-63113G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141149478 | ||||||
| chr7:141149546
|
A | G | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-63045A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141149546 | ||||||
| chr7:141149800
|
A | G | 2 | a0001c0002t0003g0052a0001c0002t0017g0062 | 2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.383-62791A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141149800 | ||||||
| chr7:141150078
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-62513C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141150078 | ||||||
| chr7:141150174
|
G | C | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.383-62417G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141150174 | ||||||
| chr7:141150749
|
G | A | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383-61842G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141150749 | ||||||
| chr7:141151215
|
C | T | 1 | a0001c0001t0014g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.383-61376C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141151215 | ||||||
| chr7:141151713
|
G | C | 2 | a0001c0001t0023g0018a0001c0004t0043g0032 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.383-60878G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141151713 | ||||||
| chr7:141151991
|
A | G | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.383-60600A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141151991 | ||||||
| chr7:141151999
|
C | T | 1 | a0001c0002t0010g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.383-60592C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141151999 | ||||||
| chr7:141152267
|
G | A | 12 | a0001c0001t0010g0021a0001c0002t0001g0057a0001c0002t0001g0064others(9): Show | 12 | HG01106.hp1 HG01243.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.383-60324G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141152267 | ||||||
| chr7:141152803
|
G | A | 1 | a0001c0002t0011g0044 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.383-59788G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141152803 | ||||||
| chr7:141153012
|
A | G | 9 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.383-59579A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141153012 | ||||||
| chr7:141153097
|
G | A | 2 | a0001c0002t0001g0064a0001c0002t0027g0051 | 2 | HG02486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.383-59494G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141153097 | ||||||
| chr7:141153195
|
T | C | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.383-59396T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141153195 | ||||||
| chr7:141153241
|
C | A | 9 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.383-59350C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141153241 | ||||||
| chr7:141153282
|
G | T | 4 | a0001c0002t0001g0076a0001c0002t0008g0003a0001c0002t0024g0002others(1): Show | 4 | HG03579.hp1 NA18522.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-59309G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141153282 | ||||||
| chr7:141153426
|
G | A | 2 | a0001c0001t0023g0018a0001c0004t0043g0032 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.383-59165G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141153426 | ||||||
| chr7:141154106
|
A | T | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-58485A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141154106 | ||||||
| chr7:141154620
|
C | T | 7 | a0001c0002t0001g0057a0001c0002t0007g0053a0001c0002t0007g0073others(4): Show | 7 | HG01106.hp1 HG01255.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.383-57971C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141154620 | ||||||
| chr7:141154638
|
G | C | 2 | a0001c0001t0023g0018a0001c0004t0043g0032 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.383-57953G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141154638 | ||||||
| chr7:141154875
|
G | A | 2 | a0001c0001t0001g0012a0001c0005t0001g0005 | 2 | HG01106.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.383-57716G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141154875 | ||||||
| chr7:141154940
|
G | C | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.383-57651G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141154940 | ||||||
| chr7:141155294
|
G | A | 54 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(51): Show | 54 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.383-57297G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141155294 | ||||||
| chr7:141155463
|
C | T | 54 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(51): Show | 54 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.383-57128C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141155463 | ||||||
| chr7:141155476
|
G | GT | 3 | a0001c0001t0006g0025a0001c0001t0033g0031a0001c0002t0006g0040 | 3 | HG02630.hp1 HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.383-57112dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141155476 | |||||
| chr7:141155588
|
G | A | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-57003G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141155588 | ||||||
| chr7:141155654
|
C | T | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383-56937C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141155654 | ||||||
| chr7:141155786
|
C | T | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.383-56805C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141155786 | ||||||
| chr7:141155997
|
G | A | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-56594G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141155997 | ||||||
| chr7:141156013
|
C | T | 45 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(42): Show | 45 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.383-56578C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141156013 | ||||||
| chr7:141156781
|
A | G | 45 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(42): Show | 45 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.383-55810A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141156781 | ||||||
| chr7:141156933
|
G | A | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383-55658G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141156933 | ||||||
| chr7:141157074
|
G | A | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383-55517G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141157074 | ||||||
| chr7:141157341
|
G | T | 45 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(42): Show | 45 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.383-55250G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141157341 | ||||||
| chr7:141157427
|
GCA | G | 9 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.383-55150_383-5514 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141157427 | |||||
| chr7:141157431
|
A | ACACACAC others(5): Show |
1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-55142_383-5513 others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141157431 | |||||
| chr7:141157443
|
G | A | 3 | a0001c0001t0014g0033a0001c0001t0028g0022a0001c0002t0005g0049 | 3 | HG01243.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.383-55148G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141157443 | ||||||
| chr7:141157454
|
C | T | 1 | a0001c0002t0031g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.383-55137C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141157454 | ||||||
| chr7:141158157
|
G | A | 45 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(42): Show | 45 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.383-54434G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141158157 | ||||||
| chr7:141158482
|
A | T | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383-54109A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141158482 | ||||||
| chr7:141159044
|
T | C | 55 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(52): Show | 55 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.383-53547T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141159044 | ||||||
| chr7:141159079
|
C | G | 80 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(77): Show | 80 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.383-53512C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141159079 | ||||||
| chr7:141159397
|
C | T | 1 | a0001c0002t0001g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.383-53194C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141159397 | ||||||
| chr7:141159537
|
C | T | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-53054C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141159537 | ||||||
| chr7:141159683
|
C | T | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383-52908C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141159683 | ||||||
| chr7:141160055
|
AAT | A | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-52524_383-5252 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141160055 | |||||
| chr7:141160098
|
GT | G | 7 | a0001c0001t0002g0027a0001c0001t0006g0025a0001c0001t0015g0028others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.383-52490delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141160098 | |||||
| chr7:141160103
|
G | T | 7 | a0001c0001t0002g0027a0001c0001t0006g0025a0001c0001t0015g0028others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.383-52488G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141160103 | ||||||
| chr7:141160169
|
G | A | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-52422G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141160169 | ||||||
| chr7:141160245
|
C | G | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.383-52346C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141160245 | ||||||
| chr7:141160525
|
C | T | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-52066C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141160525 | ||||||
| chr7:141160569
|
G | C | 7 | a0001c0001t0002g0027a0001c0001t0006g0025a0001c0001t0015g0028others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.383-52022G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141160569 | ||||||
| chr7:141160774
|
T | C | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-51817T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141160774 | ||||||
| chr7:141160811
|
G | A | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-51780G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141160811 | ||||||
| chr7:141161097
|
C | T | 66 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(63): Show | 66 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.383-51494C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141161097 | ||||||
| chr7:141161136
|
C | T | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-51455C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141161136 | ||||||
| chr7:141161432
|
G | A | 7 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(4): Show | 7 | HG01255.hp2 HG01952.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.383-51159G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141161432 | ||||||
| chr7:141161619
|
G | C | 1 | a0001c0002t0009g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.383-50972G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141161619 | ||||||
| chr7:141161864
|
G | A | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383-50727G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141161864 | ||||||
| chr7:141161908
|
G | A | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-50683G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141161908 | ||||||
| chr7:141161959
|
TGA | T | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-50628_383-5062 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141161959 | |||||
| chr7:141161978
|
G | A | 3 | a0001c0001t0001g0080a0001c0002t0002g0043a0001c0002t0041g0058 | 3 | HG00544.hp1 HG02027.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.383-50613G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141161978 | ||||||
| chr7:141162084
|
C | T | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-50507C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141162084 | ||||||
| chr7:141162116
|
C | A | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-50475C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141162116 | ||||||
| chr7:141162302
|
C | A | 5 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0021g0077others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.383-50289C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141162302 | ||||||
| chr7:141162593
|
A | G | 1 | a0001c0001t0021g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.383-49998A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141162593 | ||||||
| chr7:141162933
|
A | G | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-49658A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141162933 | ||||||
| chr7:141163057
|
A | G | 2 | a0001c0002t0003g0052a0001c0002t0017g0062 | 2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.383-49534A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141163057 | ||||||
| chr7:141163064
|
C | A | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-49527C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141163064 | ||||||
| chr7:141163161
|
G | A | 4 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0037g0075others(1): Show | 4 | HG00544.hp2 HG01256.hp1 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-49430G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141163161 | ||||||
| chr7:141163188
|
G | A | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.383-49403G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141163188 | ||||||
| chr7:141163313
|
A | T | 1 | a0001c0002t0037g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.383-49278A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141163313 | ||||||
| chr7:141163446
|
G | A | 5 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0021g0077others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.383-49145G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141163446 | ||||||
| chr7:141163510
|
C | G | 2 | a0001c0001t0008g0004a0001c0001t0044g0001 | 2 | HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.383-49081C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141163510 | ||||||
| chr7:141163641
|
A | C | 9 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.383-48950A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141163641 | ||||||
| chr7:141163686
|
T | A | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-48905T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141163686 | ||||||
| chr7:141163846
|
G | A | 44 | a0001c0001t0002g0027a0001c0001t0003g0007a0001c0001t0003g0020others(41): Show | 44 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.383-48745G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141163846 | ||||||
| chr7:141164001
|
C | A | 1 | a0001c0001t0001g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.383-48590C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141164001 | ||||||
| chr7:141164563
|
A | G | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-48028A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141164563 | ||||||
| chr7:141164736
|
A | G | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-47855A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141164736 | ||||||
| chr7:141165172
|
T | C | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-47419T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141165172 | ||||||
| chr7:141165189
|
T | TC | 57 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(54): Show | 57 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.383-47400dupC | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141165189 | |||||
| chr7:141165378
|
C | T | 1 | a0001c0001t0009g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.383-47213C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141165378 | ||||||
| chr7:141165385
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.383-47206G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141165385 | ||||||
| chr7:141165750
|
G | A | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-46841G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141165750 | ||||||
| chr7:141165952
|
C | T | 44 | a0001c0001t0002g0027a0001c0001t0003g0007a0001c0001t0003g0020others(41): Show | 44 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.383-46639C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141165952 | ||||||
| chr7:141166274
|
A | G | 1 | a0001c0002t0041g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.383-46317A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141166274 | ||||||
| chr7:141166361
|
G | A | 2 | a0001c0001t0014g0033a0001c0001t0028g0022 | 2 | HG01243.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.383-46230G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141166361 | ||||||
| chr7:141166638
|
A | G | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-45953A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141166638 | ||||||
| chr7:141166641
|
G | A | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-45950G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141166641 | ||||||
| chr7:141167495
|
A | G | 3 | a0001c0001t0014g0033a0001c0001t0028g0022a0001c0002t0005g0049 | 3 | HG01243.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.383-45096A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141167495 | ||||||
| chr7:141167523
|
A | G | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.383-45068A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141167523 | ||||||
| chr7:141168112
|
C | T | 1 | a0001c0001t0005g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.383-44479C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141168112 | ||||||
| chr7:141168164
|
G | A | 1 | a0001c0001t0004g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.383-44427G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141168164 | ||||||
| chr7:141168325
|
A | G | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.383-44266A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141168325 | ||||||
| chr7:141168625
|
C | T | 9 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.383-43966C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141168625 | ||||||
| chr7:141168627
|
G | A | 9 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.383-43964G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141168627 | ||||||
| chr7:141168749
|
G | A | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383-43842G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141168749 | ||||||
| chr7:141168840
|
T | C | 8 | a0001c0001t0003g0007a0001c0001t0010g0021a0001c0001t0038g0034others(5): Show | 8 | HG02083.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.383-43751T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141168840 | ||||||
| chr7:141168932
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.383-43659C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141168932 | ||||||
| chr7:141169144
|
G | A | 55 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(52): Show | 55 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.383-43447G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141169144 | ||||||
| chr7:141170518
|
C | T | 1 | a0001c0001t0003g0020 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.383-42073C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141170518 | ||||||
| chr7:141170588
|
C | T | 10 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0006g0017others(7): Show | 10 | HG01106.hp2 HG01255.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.383-42003C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141170588 | ||||||
| chr7:141170745
|
C | T | 44 | a0001c0001t0002g0027a0001c0001t0003g0007a0001c0001t0003g0020others(41): Show | 44 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.383-41846C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141170745 | ||||||
| chr7:141171017
|
TACACAC | T | 4 | a0001c0001t0001g0038a0001c0001t0008g0030a0001c0001t0012g0036others(1): Show | 4 | HG02083.hp1 HG02523.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-41531_383-4152 others(10): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141171017 | |||||
| chr7:141171017
|
TACACACA others(1): Show |
T | 23 | a0001c0001t0001g0015a0001c0001t0001g0080a0001c0001t0005g0008others(20): Show | 23 | HG00544.hp1 HG01255.hp2 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.383-41533_383-4152 others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141171017 | |||||
| chr7:141171017
|
TACACACA others(3): Show |
T | 7 | a0001c0001t0001g0012a0001c0001t0008g0004a0001c0001t0016g0037others(4): Show | 7 | HG01106.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.383-41535_383-4152 others(14): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141171017 | |||||
| chr7:141171017
|
TACACACA others(9): Show |
T | 44 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(41): Show | 44 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.383-41541_383-4152 others(20): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141171017 | |||||
| chr7:141171017
|
TACACACA others(13): Show |
T | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.383-41545_383-4152 others(24): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141171017 | |||||
| chr7:141171050
|
ACACACAC others(8): Show |
A | 1 | a0001c0002t0007g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.383-41539_383-4152 others(19): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141171050 | |||||
| chr7:141171771
|
G | A | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-40820G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141171771 | ||||||
| chr7:141171832
|
A | G | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-40759A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141171832 | ||||||
| chr7:141171840
|
GTGAATGA others(1): Show |
G | 44 | a0001c0001t0002g0027a0001c0001t0003g0007a0001c0001t0003g0020others(41): Show | 44 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.383-40730_383-4072 others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141171840 | |||||
| chr7:141172221
|
T | C | 1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.383-40370T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141172221 | ||||||
| chr7:141173439
|
C | T | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.383-39152C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141173439 | ||||||
| chr7:141173740
|
G | A | 1 | a0001c0002t0032g0071 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.383-38851G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141173740 | ||||||
| chr7:141174445
|
A | G | 1 | a0001c0001t0011g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.383-38146A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141174445 | ||||||
| chr7:141174454
|
T | A | 1 | a0001c0002t0032g0071 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.383-38137T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141174454 | ||||||
| chr7:141174809
|
G | T | 48 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(45): Show | 48 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.383-37782G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141174809 | ||||||
| chr7:141175065
|
G | A | 2 | a0001c0001t0003g0007a0001c0002t0030g0067 | 2 | HG02109.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.383-37526G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141175065 | ||||||
| chr7:141176551
|
A | G | 1 | a0001c0001t0014g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.383-36040A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141176551 | ||||||
| chr7:141177103
|
C | T | 2 | a0001c0002t0001g0064a0001c0002t0027g0051 | 2 | HG02486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.383-35488C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141177103 | ||||||
| chr7:141177197
|
A | G | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.383-35394A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141177197 | ||||||
| chr7:141177207
|
G | C | 1 | a0001c0002t0001g0057 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.383-35384G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141177207 | ||||||
| chr7:141178088
|
C | T | 55 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(52): Show | 55 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.383-34503C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141178088 | ||||||
| chr7:141178203
|
C | T | 2 | a0001c0001t0044g0001a0001c0002t0026g0041 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.383-34388C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141178203 | ||||||
| chr7:141178795
|
G | A | 1 | a0001c0002t0007g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.383-33796G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141178795 | ||||||
| chr7:141179590
|
G | A | 47 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(44): Show | 47 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.383-33001G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141179590 | ||||||
| chr7:141179654
|
G | T | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-32937G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141179654 | ||||||
| chr7:141179844
|
T | C | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-32747T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141179844 | ||||||
| chr7:141180148
|
G | A | 1 | a0001c0002t0012g0045 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.383-32443G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141180148 | ||||||
| chr7:141180283
|
T | A | 1 | a0001c0001t0007g0011 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.383-32308T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141180283 | ||||||
| chr7:141180391
|
T | C | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-32200T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141180391 | ||||||
| chr7:141180463
|
CA | C | 43 | a0001c0001t0002g0019a0001c0001t0002g0027a0001c0001t0003g0007others(40): Show | 43 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.383-32108delA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141180463 | |||||
| chr7:141180463
|
CAA | C | 11 | a0001c0001t0001g0035a0001c0001t0004g0023a0001c0001t0008g0030others(8): Show | 11 | HG01891.hp1 HG01952.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.383-32109_383-3210 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141180463 | |||||
| chr7:141180978
|
C | T | 2 | a0001c0002t0007g0073a0001c0003t0001g0074 | 2 | HG01106.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.383-31613C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141180978 | ||||||
| chr7:141181156
|
A | G | 1 | a0001c0002t0013g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.383-31435A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141181156 | ||||||
| chr7:141181192
|
G | A | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383-31399G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141181192 | ||||||
| chr7:141182129
|
A | G | 46 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(43): Show | 46 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.383-30462A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141182129 | ||||||
| chr7:141182154
|
T | G | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-30437T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141182154 | ||||||
| chr7:141182346
|
G | A | 1 | a0002c0006t0039g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.383-30245G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141182346 | ||||||
| chr7:141182620
|
A | T | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-29971A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141182620 | ||||||
| chr7:141182717
|
C | T | 5 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0021g0077others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.383-29874C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141182717 | ||||||
| chr7:141182725
|
C | T | 2 | a0001c0001t0001g0012a0001c0005t0001g0005 | 2 | HG01106.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.383-29866C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141182725 | ||||||
| chr7:141182938
|
A | G | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-29653A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141182938 | ||||||
| chr7:141183130
|
T | C | 2 | a0001c0002t0003g0052a0001c0002t0017g0062 | 2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.383-29461T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141183130 | ||||||
| chr7:141183266
|
C | T | 57 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(54): Show | 57 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.383-29325C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141183266 | ||||||
| chr7:141183270
|
C | T | 1 | a0001c0001t0034g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.383-29321C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141183270 | ||||||
| chr7:141183339
|
A | C | 4 | a0001c0001t0015g0028a0001c0001t0029g0026a0001c0001t0033g0031others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-29252A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141183339 | ||||||
| chr7:141183618
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-28973C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141183618 | ||||||
| chr7:141183741
|
T | C | 1 | a0001c0002t0031g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.383-28850T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141183741 | ||||||
| chr7:141183861
|
A | G | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.383-28730A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141183861 | ||||||
| chr7:141184362
|
A | G | 9 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.383-28229A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141184362 | ||||||
| chr7:141184835
|
G | C | 5 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0021g0077others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.383-27756G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141184835 | ||||||
| chr7:141185408
|
G | A | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.383-27183G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141185408 | ||||||
| chr7:141185516
|
T | C | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.383-27075T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141185516 | ||||||
| chr7:141185525
|
G | C | 55 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(52): Show | 55 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.383-27066G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141185525 | ||||||
| chr7:141185604
|
A | G | 3 | a0001c0001t0014g0033a0001c0001t0028g0022a0001c0002t0005g0049 | 3 | HG01243.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.383-26987A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141185604 | ||||||
| chr7:141187005
|
T | C | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-25586T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141187005 | ||||||
| chr7:141187114
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.383-25477C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141187114 | ||||||
| chr7:141187187
|
T | C | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-25404T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141187187 | ||||||
| chr7:141187531
|
T | A | 4 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0021g0077others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-25060T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141187531 | ||||||
| chr7:141187636
|
A | C | 9 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.383-24955A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141187636 | ||||||
| chr7:141188031
|
G | C | 2 | a0001c0002t0001g0064a0001c0002t0027g0051 | 2 | HG02486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.383-24560G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141188031 | ||||||
| chr7:141188103
|
T | C | 1 | a0001c0002t0041g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.383-24488T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141188103 | ||||||
| chr7:141188216
|
C | T | 2 | a0001c0001t0004g0023a0001c0001t0004g0029 | 2 | HG01952.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.383-24375C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141188216 | ||||||
| chr7:141188395
|
T | C | 1 | a0001c0001t0007g0011 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.383-24196T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141188395 | ||||||
| chr7:141188521
|
C | G | 2 | a0001c0001t0001g0080a0001c0002t0041g0058 | 2 | HG00544.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.383-24070C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141188521 | ||||||
| chr7:141188637
|
A | G | 47 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(44): Show | 47 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.383-23954A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141188637 | ||||||
| chr7:141189067
|
A | T | 9 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0004g0029others(6): Show | 9 | HG01884.hp2 HG01952.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.383-23524A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141189067 | ||||||
| chr7:141189313
|
C | T | 55 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(52): Show | 55 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.383-23278C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141189313 | ||||||
| chr7:141189347
|
G | T | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-23244G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141189347 | ||||||
| chr7:141189406
|
G | T | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.383-23185G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141189406 | ||||||
| chr7:141189433
|
A | C | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-23158A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141189433 | ||||||
| chr7:141189459
|
A | G | 1 | a0001c0001t0012g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.383-23132A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141189459 | ||||||
| chr7:141189548
|
G | C | 2 | a0001c0001t0003g0020a0001c0001t0009g0078 | 2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.383-23043G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141189548 | ||||||
| chr7:141189736
|
C | T | 46 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(43): Show | 46 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.383-22855C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141189736 | ||||||
| chr7:141189965
|
C | G | 1 | a0001c0002t0041g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.383-22626C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141189965 | ||||||
| chr7:141190579
|
C | G | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-22012C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141190579 | ||||||
| chr7:141190605
|
C | G | 47 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(44): Show | 47 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.383-21986C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141190605 | ||||||
| chr7:141190613
|
T | C | 1 | a0001c0001t0034g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.383-21978T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141190613 | ||||||
| chr7:141190662
|
G | A | 44 | a0001c0001t0002g0027a0001c0001t0003g0007a0001c0001t0003g0020others(41): Show | 44 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.383-21929G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141190662 | ||||||
| chr7:141191196
|
G | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-21395G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141191196 | ||||||
| chr7:141192423
|
G | A | 1 | a0001c0002t0005g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.383-20168G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141192423 | ||||||
| chr7:141192490
|
CTT | C | 56 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.383-20086_383-2008 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141192490 | |||||
| chr7:141192796
|
G | A | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383-19795G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141192796 | ||||||
| chr7:141192861
|
C | T | 1 | a0001c0002t0001g0057 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.383-19730C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141192861 | ||||||
| chr7:141192887
|
C | A | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.383-19704C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141192887 | ||||||
| chr7:141193108
|
C | T | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.383-19483C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141193108 | ||||||
| chr7:141193139
|
T | C | 1 | a0001c0001t0004g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.383-19452T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141193139 | ||||||
| chr7:141193332
|
C | T | 46 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(43): Show | 46 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.383-19259C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141193332 | ||||||
| chr7:141193440
|
G | A | 1 | a0001c0002t0031g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.383-19151G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141193440 | ||||||
| chr7:141194423
|
A | T | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383-18168A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141194423 | ||||||
| chr7:141194672
|
A | T | 1 | a0001c0001t0003g0020 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.383-17919A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141194672 | ||||||
| chr7:141194704
|
G | A | 4 | a0001c0001t0005g0008a0001c0001t0025g0010a0001c0001t0034g0009others(1): Show | 4 | HG02486.hp1 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-17887G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141194704 | ||||||
| chr7:141195006
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-17585C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141195006 | ||||||
| chr7:141195256
|
A | G | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-17335A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141195256 | ||||||
| chr7:141195510
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.383-17081C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141195510 | ||||||
| chr7:141195594
|
G | A | 80 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(77): Show | 80 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.383-16997G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141195594 | ||||||
| chr7:141196057
|
G | C | 50 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(47): Show | 50 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.383-16534G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141196057 | ||||||
| chr7:141196153
|
A | G | 1 | a0001c0001t0004g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.383-16438A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141196153 | ||||||
| chr7:141196165
|
T | G | 9 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.383-16426T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141196165 | ||||||
| chr7:141196555
|
G | A | 50 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(47): Show | 50 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.383-16036G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141196555 | ||||||
| chr7:141196922
|
G | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-15669G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141196922 | ||||||
| chr7:141197129
|
C | T | 50 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(47): Show | 50 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.383-15462C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141197129 | ||||||
| chr7:141197270
|
T | C | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.383-15321T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141197270 | ||||||
| chr7:141197586
|
T | C | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383-15005T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141197586 | ||||||
| chr7:141197661
|
C | T | 3 | a0001c0001t0014g0033a0001c0001t0028g0022a0001c0002t0005g0049 | 3 | HG01243.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.383-14930C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141197661 | ||||||
| chr7:141197917
|
G | A | 9 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.383-14674G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141197917 | ||||||
| chr7:141198055
|
CCTCT | C | 39 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(36): Show | 39 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.383-14527_383-1452 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141198055 | |||||
| chr7:141198739
|
A | G | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.383-13852A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141198739 | ||||||
| chr7:141198850
|
C | T | 10 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.383-13741C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141198850 | ||||||
| chr7:141198854
|
C | T | 3 | a0001c0001t0001g0080a0001c0002t0002g0043a0001c0002t0041g0058 | 3 | HG00544.hp1 HG02027.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.383-13737C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141198854 | ||||||
| chr7:141198943
|
T | G | 1 | a0001c0002t0036g0069 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.383-13648T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141198943 | ||||||
| chr7:141199052
|
G | A | 9 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.383-13539G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141199052 | ||||||
| chr7:141199096
|
A | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-13495A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141199096 | ||||||
| chr7:141199101
|
G | A | 1 | a0001c0001t0004g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.383-13490G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141199101 | ||||||
| chr7:141199122
|
G | A | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.383-13469G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141199122 | ||||||
| chr7:141199335
|
G | A | 3 | a0001c0002t0001g0076a0001c0002t0016g0072a0002c0006t0039g0061 | 3 | HG01261.hp2 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.383-13256G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141199335 | ||||||
| chr7:141199463
|
T | A | 40 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(37): Show | 40 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.383-13128T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141199463 | ||||||
| chr7:141199862
|
T | C | 1 | a0001c0002t0013g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.383-12729T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141199862 | ||||||
| chr7:141200138
|
G | C | 50 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(47): Show | 50 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.383-12453G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141200138 | ||||||
| chr7:141200255
|
C | G | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-12336C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141200255 | ||||||
| chr7:141200284
|
G | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-12307G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141200284 | ||||||
| chr7:141200517
|
A | T | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-12074A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141200517 | ||||||
| chr7:141200753
|
G | C | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-11838G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141200753 | ||||||
| chr7:141200899
|
G | A | 4 | a0001c0001t0022g0013a0001c0002t0007g0053a0001c0002t0032g0071others(1): Show | 4 | HG01255.hp1 HG01261.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-11692G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141200899 | ||||||
| chr7:141200920
|
A | G | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-11671A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141200920 | ||||||
| chr7:141201078
|
G | A | 1 | a0001c0002t0012g0045 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.383-11513G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141201078 | ||||||
| chr7:141201153
|
C | T | 5 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0021g0077others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.383-11438C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141201153 | ||||||
| chr7:141201302
|
G | A | 2 | a0001c0001t0001g0012a0001c0005t0001g0005 | 2 | HG01106.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.383-11289G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141201302 | ||||||
| chr7:141201715
|
G | A | 1 | a0001c0002t0037g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.383-10876G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141201715 | ||||||
| chr7:141201756
|
A | C | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-10835A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141201756 | ||||||
| chr7:141201823
|
G | A | 5 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0021g0077others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.383-10768G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141201823 | ||||||
| chr7:141201868
|
G | A | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-10723G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141201868 | ||||||
| chr7:141201959
|
T | A | 4 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0021g0077others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-10632T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141201959 | ||||||
| chr7:141202000
|
G | C | 2 | a0001c0001t0023g0018a0001c0004t0043g0032 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.383-10591G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141202000 | ||||||
| chr7:141202043
|
C | T | 39 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(36): Show | 39 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.383-10548C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141202043 | ||||||
| chr7:141202209
|
G | T | 1 | a0001c0002t0008g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.383-10382G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141202209 | ||||||
| chr7:141202245
|
C | G | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383-10346C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141202245 | ||||||
| chr7:141202393
|
A | G | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.383-10198A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141202393 | ||||||
| chr7:141202572
|
G | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-10019G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141202572 | ||||||
| chr7:141202841
|
A | G | 14 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(11): Show | 14 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.383-9750A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141202841 | ||||||
| chr7:141202929
|
C | G | 11 | a0001c0001t0008g0004a0001c0001t0008g0030a0001c0001t0014g0039others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-9662C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141202929 | ||||||
| chr7:141202944
|
A | T | 40 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(37): Show | 40 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.383-9647A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141202944 | ||||||
| chr7:141202952
|
G | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-9639G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141202952 | ||||||
| chr7:141203164
|
A | C | 1 | a0001c0001t0035g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.383-9427A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141203164 | ||||||
| chr7:141203186
|
C | T | 3 | a0001c0001t0016g0037a0001c0001t0021g0077a0001c0002t0010g0066 | 3 | HG01891.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.383-9405C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141203186 | ||||||
| chr7:141203288
|
T | C | 40 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(37): Show | 40 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.383-9303T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141203288 | ||||||
| chr7:141203456
|
T | C | 42 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(39): Show | 42 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.383-9135T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141203456 | ||||||
| chr7:141203545
|
G | C | 1 | a0001c0003t0001g0074 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.383-9046G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141203545 | ||||||
| chr7:141203578
|
G | A | 43 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(40): Show | 43 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.383-9013G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141203578 | ||||||
| chr7:141203613
|
G | A | 2 | a0001c0001t0014g0033a0001c0001t0028g0022 | 2 | HG01243.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.383-8978G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141203613 | ||||||
| chr7:141203803
|
C | T | 2 | a0001c0001t0044g0001a0001c0002t0026g0041 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.383-8788C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141203803 | ||||||
| chr7:141203810
|
A | G | 42 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(39): Show | 42 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.383-8781A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141203810 | ||||||
| chr7:141203818
|
G | A | 40 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(37): Show | 40 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.383-8773G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141203818 | ||||||
| chr7:141203878
|
G | A | 42 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(39): Show | 42 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.383-8713G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141203878 | ||||||
| chr7:141203916
|
A | C | 43 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(40): Show | 43 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.383-8675A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141203916 | ||||||
| chr7:141203971
|
T | C | 54 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(51): Show | 54 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.383-8620T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141203971 | ||||||
| chr7:141204048
|
A | G | 2 | a0001c0001t0003g0007a0001c0002t0030g0067 | 2 | HG02109.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.383-8543A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141204048 | ||||||
| chr7:141204171
|
G | A | 1 | a0001c0002t0006g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.383-8420G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141204171 | ||||||
| chr7:141204223
|
G | A | 42 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(39): Show | 42 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.383-8368G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141204223 | ||||||
| chr7:141204282
|
G | A | 42 | a0001c0001t0001g0035a0001c0001t0003g0007a0001c0001t0003g0020others(39): Show | 42 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.383-8309G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141204282 | ||||||
| chr7:141204343
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-8248C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141204343 | ||||||
| chr7:141204345
|
A | G | 1 | a0001c0001t0014g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.383-8246A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141204345 | ||||||
| chr7:141204441
|
G | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-8150G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141204441 | ||||||
| chr7:141204446
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-8145C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141204446 | ||||||
| chr7:141204479
|
G | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-8112G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141204479 | ||||||
| chr7:141204544
|
A | G | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-8047A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141204544 | ||||||
| chr7:141204600
|
T | C | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-7991T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141204600 | ||||||
| chr7:141204621
|
C | T | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.383-7970C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141204621 | ||||||
| chr7:141204672
|
G | C | 40 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(37): Show | 40 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.383-7919G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141204672 | ||||||
| chr7:141205160
|
C | T | 43 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(40): Show | 43 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.383-7431C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141205160 | ||||||
| chr7:141205192
|
T | G | 54 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(51): Show | 54 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.383-7399T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141205192 | ||||||
| chr7:141205328
|
C | T | 42 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(39): Show | 42 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.383-7263C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141205328 | ||||||
| chr7:141205332
|
C | G | 42 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(39): Show | 42 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.383-7259C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141205332 | ||||||
| chr7:141205430
|
G | A | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.383-7161G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141205430 | ||||||
| chr7:141205463
|
C | G | 43 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(40): Show | 43 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.383-7128C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141205463 | ||||||
| chr7:141205596
|
A | C | 80 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(77): Show | 80 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.383-6995A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141205596 | ||||||
| chr7:141205615
|
C | T | 1 | a0001c0003t0018g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.383-6976C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141205615 | ||||||
| chr7:141205914
|
C | T | 39 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(36): Show | 39 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.383-6677C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141205914 | ||||||
| chr7:141206059
|
G | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-6532G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141206059 | ||||||
| chr7:141206338
|
A | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-6253A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141206338 | ||||||
| chr7:141206352
|
G | A | 40 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(37): Show | 40 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.383-6239G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141206352 | ||||||
| chr7:141206474
|
T | C | 42 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(39): Show | 42 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.383-6117T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141206474 | ||||||
| chr7:141206498
|
C | T | 42 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(39): Show | 42 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.383-6093C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141206498 | ||||||
| chr7:141206499
|
A | G | 42 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(39): Show | 42 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.383-6092A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141206499 | ||||||
| chr7:141206531
|
G | A | 42 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(39): Show | 42 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.383-6060G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141206531 | ||||||
| chr7:141206590
|
T | C | 42 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(39): Show | 42 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.383-6001T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141206590 | ||||||
| chr7:141206598
|
G | A | 1 | a0001c0003t0018g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.383-5993G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141206598 | ||||||
| chr7:141206624
|
G | A | 40 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(37): Show | 40 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.383-5967G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141206624 | ||||||
| chr7:141206689
|
A | G | 42 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(39): Show | 42 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.383-5902A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141206689 | ||||||
| chr7:141206707
|
G | C | 42 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(39): Show | 42 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.383-5884G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141206707 | ||||||
| chr7:141206876
|
T | C | 2 | a0001c0001t0044g0001a0001c0002t0026g0041 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.383-5715T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141206876 | ||||||
| chr7:141206954
|
G | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-5637G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141206954 | ||||||
| chr7:141207075
|
T | C | 40 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(37): Show | 40 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.383-5516T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141207075 | ||||||
| chr7:141207096
|
T | C | 2 | a0001c0001t0044g0001a0001c0002t0026g0041 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.383-5495T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141207096 | ||||||
| chr7:141207130
|
G | T | 40 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(37): Show | 40 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.383-5461G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141207130 | ||||||
| chr7:141207511
|
A | G | 2 | a0001c0001t0044g0001a0001c0002t0026g0041 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.383-5080A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141207511 | ||||||
| chr7:141207652
|
T | C | 2 | a0001c0001t0044g0001a0001c0002t0026g0041 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.383-4939T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141207652 | ||||||
| chr7:141207741
|
CA | C | 2 | a0001c0001t0044g0001a0001c0002t0026g0041 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.383-4849delA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141207741 | ||||||
| chr7:141207821
|
A | C | 2 | a0001c0001t0044g0001a0001c0002t0026g0041 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.383-4770A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141207821 | ||||||
| chr7:141207994
|
A | T | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.383-4597A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141207994 | ||||||
| chr7:141208082
|
A | G | 2 | a0001c0001t0044g0001a0001c0002t0026g0041 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.383-4509A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141208082 | ||||||
| chr7:141208195
|
TTAAA | T | 40 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(37): Show | 40 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.383-4372_383-4369d others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141208195 | |||||
| chr7:141208195
|
TTAAATAA others(5): Show |
T | 2 | a0001c0001t0044g0001a0001c0002t0026g0041 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.383-4380_383-4369d others(14): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141208195 | |||||
| chr7:141208304
|
A | C | 39 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(36): Show | 39 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.383-4287A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141208304 | ||||||
| chr7:141208975
|
G | A | 2 | a0001c0001t0044g0001a0001c0002t0026g0041 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.383-3616G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141208975 | ||||||
| chr7:141209080
|
G | GT | 3 | a0001c0001t0005g0014a0001c0002t0015g0056a0001c0002t0040g0050 | 3 | HG03139.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.383-3508dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 141209080 | |||||
| chr7:141209137
|
C | T | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383-3454C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141209137 | ||||||
| chr7:141209308
|
C | G | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.383-3283C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141209308 | ||||||
| chr7:141209351
|
C | T | 10 | a0001c0001t0008g0004a0001c0001t0014g0039a0001c0001t0015g0028others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.383-3240C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141209351 | ||||||
| chr7:141209462
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-3129C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141209462 | ||||||
| chr7:141209983
|
G | A | 40 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(37): Show | 40 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.383-2608G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141209983 | ||||||
| chr7:141210230
|
C | T | 13 | a0001c0001t0008g0004a0001c0001t0014g0039a0001c0001t0015g0028others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.383-2361C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141210230 | ||||||
| chr7:141210350
|
G | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-2241G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141210350 | ||||||
| chr7:141210395
|
G | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-2196G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141210395 | ||||||
| chr7:141210420
|
G | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-2171G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141210420 | ||||||
| chr7:141210488
|
A | G | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-2103A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141210488 | ||||||
| chr7:141210504
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-2087C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141210504 | ||||||
| chr7:141210523
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-2068C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141210523 | ||||||
| chr7:141210755
|
C | G | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-1836C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141210755 | ||||||
| chr7:141210887
|
C | T | 43 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(40): Show | 43 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.383-1704C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141210887 | ||||||
| chr7:141210970
|
G | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-1621G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141210970 | ||||||
| chr7:141211313
|
A | G | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-1278A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141211313 | ||||||
| chr7:141211563
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-1028C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141211563 | ||||||
| chr7:141211628
|
G | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-963G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141211628 | ||||||
| chr7:141211761
|
G | A | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.383-830G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141211761 | ||||||
| chr7:141212056
|
C | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.383-535C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141212056 | ||||||
| chr7:141212080
|
G | T | 1 | a0001c0001t0001g0038 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.383-511G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141212080 | ||||||
| chr7:141212371
|
G | A | 1 | a0001c0002t0013g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.383-220G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141212371 | ||||||
| chr7:141212479
|
A | G | 2 | a0001c0001t0044g0001a0001c0002t0026g0041 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.383-112A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 1/3 | chr7 | 141212479 | ||||||
| chr7:141213116
|
G | A | 2 | a0001c0002t0015g0056a0001c0002t0040g0050 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.496+412G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141213116 | ||||||
| chr7:141213215
|
A | G | 2 | a0001c0001t0044g0001a0001c0002t0026g0041 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.496+511A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141213215 | ||||||
| chr7:141213234
|
T | G | 2 | a0001c0001t0023g0018a0001c0004t0043g0032 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.496+530T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141213234 | ||||||
| chr7:141213314
|
G | C | 2 | a0001c0001t0044g0001a0001c0002t0026g0041 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.496+610G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141213314 | ||||||
| chr7:141213369
|
A | G | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.496+665A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141213369 | ||||||
| chr7:141213650
|
T | C | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+946T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141213650 | ||||||
| chr7:141213910
|
C | T | 32 | a0001c0001t0003g0007a0001c0001t0003g0020a0001c0001t0004g0024others(29): Show | 32 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.496+1206C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141213910 | ||||||
| chr7:141214009
|
T | A | 2 | a0001c0001t0008g0004a0001c0001t0044g0001 | 2 | HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.496+1305T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141214009 | ||||||
| chr7:141214478
|
A | G | 1 | a0001c0001t0020g0006 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.496+1774A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141214478 | ||||||
| chr7:141214623
|
A | G | 2 | a0001c0001t0003g0007a0001c0002t0030g0067 | 2 | HG02109.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.496+1919A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141214623 | ||||||
| chr7:141214656
|
A | G | 35 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(32): Show | 35 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.496+1952A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141214656 | ||||||
| chr7:141214739
|
G | C | 35 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(32): Show | 35 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.496+2035G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141214739 | ||||||
| chr7:141214740
|
G | A | 2 | a0001c0002t0016g0072a0002c0006t0039g0061 | 2 | HG01261.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.496+2036G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141214740 | ||||||
| chr7:141214859
|
G | A | 45 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(42): Show | 45 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.496+2155G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141214859 | ||||||
| chr7:141214941
|
G | A | 35 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(32): Show | 35 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.496+2237G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141214941 | ||||||
| chr7:141215129
|
A | G | 1 | a0001c0002t0012g0045 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.496+2425A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141215129 | ||||||
| chr7:141215337
|
A | ATTATTAT others(10): Show |
5 | a0001c0001t0022g0013a0001c0002t0007g0053a0001c0003t0001g0068others(2): Show | 5 | HG01243.hp2 HG01256.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+2635_496+2636i others(19): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215337 | |||||
| chr7:141215337
|
A | ATTATTAT others(10): Show |
5 | a0001c0002t0001g0057a0001c0002t0007g0073a0001c0002t0032g0071others(2): Show | 5 | HG01106.hp1 HG01255.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+2635_496+2636i others(19): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215337 | |||||
| chr7:141215337
|
A | ATTATTAT others(10): Show |
1 | a0001c0002t0016g0072 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.496+2635_496+2636i others(19): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215337 | |||||
| chr7:141215337
|
A | ATTATTAT others(3): Show |
1 | a0001c0005t0001g0005 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.496+2635_496+2636i others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215337 | |||||
| chr7:141215337
|
A | ATTATTTT others(3): Show |
15 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(12): Show | 15 | HG00544.hp1 HG00544.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+2635_496+2636i others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215337 | |||||
| chr7:141215337
|
A | ATTATTTT others(4): Show |
1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.496+2635_496+2636i others(13): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215337 | |||||
| chr7:141215337
|
A | ATTTTTTT others(3): Show |
6 | a0001c0001t0004g0024a0001c0002t0001g0064a0001c0002t0027g0051others(3): Show | 6 | HG02027.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+2639_496+2640i others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215337 | |||||
| chr7:141215337
|
A | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+2633A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141215337 | ||||||
| chr7:141215338
|
T | G | 1 | a0001c0002t0031g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.496+2634T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141215338 | ||||||
| chr7:141215628
|
G | A | 35 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(32): Show | 35 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.496+2924G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141215628 | ||||||
| chr7:141215644
|
C | T | 44 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(41): Show | 44 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.496+2940C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141215644 | ||||||
| chr7:141215777
|
C | CCTTT | 4 | a0001c0001t0002g0019a0001c0001t0008g0030a0001c0001t0014g0033others(1): Show | 4 | HG01243.hp1 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+3134_496+3137d others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215777 | |||||
| chr7:141215777
|
CCTTT | C | 13 | a0001c0001t0004g0029a0001c0001t0006g0025a0001c0001t0009g0078others(10): Show | 13 | HG01978.hp1 HG02027.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.496+3134_496+3137d others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215777 | |||||
| chr7:141215777
|
CCTTTCTT others(1): Show |
C | 12 | a0001c0001t0001g0012a0001c0001t0002g0027a0001c0001t0003g0007others(9): Show | 12 | HG01106.hp2 HG01261.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.496+3130_496+3137d others(10): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215777 | |||||
| chr7:141215777
|
CCTTTCTT others(5): Show |
C | 8 | a0001c0001t0004g0024a0001c0001t0005g0008a0001c0001t0007g0011others(5): Show | 8 | HG02027.hp1 HG02523.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+3126_496+3137d others(14): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215777 | |||||
| chr7:141215777
|
CCTTTCTT others(9): Show |
C | 3 | a0001c0001t0010g0021a0001c0002t0008g0003a0001c0002t0042g0054 | 3 | HG03516.hp1 HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.496+3122_496+3137d others(18): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215777 | |||||
| chr7:141215777
|
CCTTTCTT others(13): Show |
C | 2 | a0001c0001t0038g0034a0001c0002t0013g0047 | 2 | HG00544.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.496+3118_496+3137d others(22): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215777 | |||||
| chr7:141215777
|
CCTTTCTT others(17): Show |
C | 2 | a0001c0002t0001g0064a0001c0002t0027g0051 | 2 | HG02486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.496+3114_496+3137d others(26): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215777 | |||||
| chr7:141215777
|
CCTTTCTT others(25): Show |
C | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.496+3106_496+3137d others(34): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215777 | |||||
| chr7:141215785
|
T | C | 2 | a0001c0002t0011g0044a0001c0002t0037g0075 | 2 | HG02027.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.496+3081T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141215785 | ||||||
| chr7:141215788
|
TTCTTTC | T | 2 | a0001c0001t0016g0037a0001c0001t0021g0077 | 2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.496+3086_496+3091d others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215788 | |||||
| chr7:141215788
|
TTCTTTCT others(3): Show |
T | 2 | a0001c0002t0002g0043a0001c0002t0010g0066 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.496+3086_496+3095d others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215788 | |||||
| chr7:141215788
|
TTCTTTCT others(7): Show |
T | 1 | a0001c0001t0014g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.496+3086_496+3099d others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215788 | |||||
| chr7:141215788
|
TTCTTTCT others(15): Show |
T | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.496+3086_496+3107d others(24): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215788 | |||||
| chr7:141215793
|
T | C | 1 | a0001c0002t0041g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.496+3089T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141215793 | ||||||
| chr7:141215797
|
T | C | 1 | a0001c0002t0041g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.496+3093T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141215797 | ||||||
| chr7:141215819
|
TTTCTTTC | T | 2 | a0001c0002t0015g0056a0001c0002t0040g0050 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.496+3118_496+3124d others(9): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215819 | |||||
| chr7:141215823
|
TTTCTTTC others(4): Show |
T | 1 | a0001c0002t0031g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.496+3122_496+3132d others(13): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215823 | |||||
| chr7:141215826
|
CTTTCTTT others(6): Show |
C | 2 | a0001c0001t0033g0031a0001c0002t0036g0069 | 2 | HG01256.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.496+3130_496+3142d others(15): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215826 | |||||
| chr7:141215831
|
TTTC | T | 6 | a0001c0001t0001g0038a0001c0002t0001g0048a0001c0002t0012g0045others(3): Show | 6 | HG01255.hp2 HG01952.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+3130_496+3132d others(5): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215831 | |||||
| chr7:141215833
|
T | C | 1 | a0001c0001t0005g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.496+3129T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141215833 | ||||||
| chr7:141215834
|
C | CT | 3 | a0001c0001t0044g0001a0001c0002t0001g0065a0001c0002t0026g0041 | 3 | HG01978.hp2 HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.496+3133dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215834 | |||||
| chr7:141215834
|
C | T | 2 | a0001c0001t0005g0014a0001c0001t0008g0004 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.496+3130C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141215834 | ||||||
| chr7:141215848
|
CT | C | 34 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(31): Show | 34 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.496+3148delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215848 | |||||
| chr7:141215853
|
C | CT | 2 | a0001c0001t0001g0015a0001c0001t0008g0030 | 2 | HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.496+3152dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215853 | |||||
| chr7:141215855
|
T | C | 1 | a0001c0003t0018g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.496+3151T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141215855 | ||||||
| chr7:141215857
|
CTCTT | C | 9 | a0001c0001t0001g0038a0001c0001t0005g0014a0001c0001t0006g0017others(6): Show | 9 | HG02083.hp2 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.496+3163_496+3166d others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215857 | |||||
| chr7:141215859
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0008g0030a0001c0002t0036g0069 | 3 | HG01256.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.496+3155C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141215859 | ||||||
| chr7:141215861
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0008g0030 | 2 | HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.496+3157T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141215861 | ||||||
| chr7:141215893
|
CTTCT | C | 35 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(32): Show | 35 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.496+3208_496+3211d others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141215893 | |||||
| chr7:141216132
|
G | C | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+3428G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216132 | ||||||
| chr7:141216221
|
A | G | 35 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(32): Show | 35 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.496+3517A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216221 | ||||||
| chr7:141216243
|
G | A | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.496+3539G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216243 | ||||||
| chr7:141216423
|
C | CTG | 5 | a0001c0001t0006g0025a0001c0001t0014g0033a0001c0001t0028g0022others(2): Show | 5 | HG01243.hp1 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+3744_496+3745d others(4): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216423 | |||||
| chr7:141216423
|
C | CTGTGTG | 2 | a0001c0001t0010g0021a0001c0001t0044g0001 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.496+3740_496+3745d others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216423 | |||||
| chr7:141216423
|
C | CTGTGTGT others(3): Show |
4 | a0001c0001t0001g0038a0001c0001t0005g0014a0001c0001t0034g0009others(1): Show | 4 | HG02602.hp2 HG02683.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+3736_496+3745d others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216423 | |||||
| chr7:141216423
|
C | CTGTGTGT others(5): Show |
6 | a0001c0001t0035g0079a0001c0002t0012g0045a0001c0002t0015g0056others(3): Show | 6 | HG02083.hp2 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+3734_496+3745d others(14): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216423 | |||||
| chr7:141216423
|
C | CTGTGTGT others(11): Show |
1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+3728_496+3745d others(20): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216423 | |||||
| chr7:141216442
|
TGTGTGTG others(13): Show |
T | 9 | a0001c0001t0022g0013a0001c0002t0001g0057a0001c0002t0007g0053others(6): Show | 9 | HG01243.hp2 HG01255.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.496+3746_496+3765d others(22): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216442 | |||||
| chr7:141216444
|
TGTGTGCG others(11): Show |
T | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.496+3746_496+3763d others(20): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216444 | |||||
| chr7:141216446
|
TGTGCGCG others(9): Show |
T | 1 | a0001c0003t0001g0074 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.496+3746_496+3761d others(18): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216446 | |||||
| chr7:141216448
|
T | TGTGTGTG others(3): Show |
1 | a0001c0002t0010g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.496+3745_496+3746i others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216448 | |||||
| chr7:141216448
|
T | TGTGTGTG others(5): Show |
1 | a0001c0001t0021g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.496+3745_496+3746i others(14): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216448 | |||||
| chr7:141216448
|
T | TGTGTGTG others(7): Show |
1 | a0001c0001t0014g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.496+3745_496+3746i others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216448 | |||||
| chr7:141216448
|
T | TGTGTGTG others(5): Show |
5 | a0001c0001t0004g0023a0001c0001t0004g0029a0001c0001t0015g0028others(2): Show | 5 | HG01884.hp2 HG01952.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+3745_496+3746i others(14): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216448 | |||||
| chr7:141216448
|
T | TGTGTGTG others(7): Show |
2 | a0001c0001t0016g0037a0001c0002t0002g0043 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.496+3745_496+3746i others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216448 | |||||
| chr7:141216448
|
T | TGTGTGTG others(11): Show |
1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.496+3745_496+3746i others(20): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216448 | |||||
| chr7:141216448
|
TGCGC | T | 3 | a0001c0001t0004g0024a0001c0002t0001g0064a0001c0002t0027g0051 | 3 | HG02486.hp2 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.496+3756_496+3759d others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216448 | |||||
| chr7:141216448
|
TGCGCGC | T | 6 | a0001c0001t0003g0020a0001c0001t0008g0004a0001c0002t0008g0003others(3): Show | 6 | HG02027.hp1 HG03209.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+3754_496+3759d others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216448 | |||||
| chr7:141216448
|
TGCGCGCG others(1): Show |
T | 4 | a0001c0001t0007g0011a0001c0002t0005g0049a0001c0002t0013g0047others(1): Show | 4 | HG00544.hp2 HG01256.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+3752_496+3759d others(10): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216448 | |||||
| chr7:141216448
|
TGCGCGCG others(3): Show |
T | 6 | a0001c0001t0003g0007a0001c0002t0003g0052a0001c0002t0017g0062others(3): Show | 6 | HG01891.hp2 HG02027.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+3750_496+3759d others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216448 | |||||
| chr7:141216448
|
TGCGCGCG others(5): Show |
T | 3 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019 | 3 | HG00544.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.496+3748_496+3759d others(14): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216448 | |||||
| chr7:141216448
|
TGCGCGCG others(7): Show |
T | 2 | a0001c0002t0007g0073a0001c0002t0011g0044 | 2 | HG02083.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.496+3746_496+3759d others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141216448 | |||||
| chr7:141216450
|
C | T | 13 | a0001c0001t0001g0038a0001c0001t0005g0014a0001c0001t0008g0030others(10): Show | 13 | HG02083.hp2 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.496+3746C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216450 | ||||||
| chr7:141216452
|
C | T | 5 | a0001c0001t0009g0078a0001c0001t0034g0009a0001c0001t0035g0079others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+3748C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216452 | ||||||
| chr7:141216454
|
C | T | 6 | a0001c0001t0004g0024a0001c0001t0009g0078a0001c0001t0034g0009others(3): Show | 6 | HG02109.hp2 HG02486.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+3750C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216454 | ||||||
| chr7:141216456
|
C | T | 9 | a0001c0001t0003g0020a0001c0001t0004g0024a0001c0001t0009g0078others(6): Show | 9 | HG02027.hp1 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.496+3752C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216456 | ||||||
| chr7:141216458
|
C | T | 13 | a0001c0001t0003g0020a0001c0001t0004g0024a0001c0001t0007g0011others(10): Show | 13 | HG00544.hp2 HG01256.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.496+3754C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216458 | ||||||
| chr7:141216460
|
C | T | 19 | a0001c0001t0003g0007a0001c0001t0003g0020a0001c0001t0004g0024others(16): Show | 19 | HG00544.hp2 HG01256.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.496+3756C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216460 | ||||||
| chr7:141216462
|
C | T | 35 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(32): Show | 35 | HG00544.hp1 HG00544.hp2 HG01256.hp2 others(32): Show |
intron_variant | MODIFIER | c.496+3758C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216462 | ||||||
| chr7:141216464
|
T | C | 2 | a0001c0001t0034g0009a0001c0004t0043g0032 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.496+3760T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216464 | ||||||
| chr7:141216476
|
G | T | 50 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(47): Show | 50 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.496+3772G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216476 | ||||||
| chr7:141216484
|
G | A | 13 | a0001c0001t0004g0023a0001c0001t0004g0029a0001c0001t0014g0039others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.496+3780G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216484 | ||||||
| chr7:141216494
|
A | G | 51 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(48): Show | 51 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.496+3790A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216494 | ||||||
| chr7:141216666
|
A | G | 35 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(32): Show | 35 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.496+3962A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216666 | ||||||
| chr7:141216818
|
G | T | 35 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(32): Show | 35 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.496+4114G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216818 | ||||||
| chr7:141216867
|
C | T | 11 | a0001c0001t0004g0023a0001c0001t0004g0029a0001c0001t0014g0039others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.496+4163C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216867 | ||||||
| chr7:141216868
|
G | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+4164G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141216868 | ||||||
| chr7:141217044
|
G | A | 23 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0004g0029others(20): Show | 23 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.496+4340G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141217044 | ||||||
| chr7:141217269
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+4565C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141217269 | ||||||
| chr7:141217285
|
G | C | 1 | a0001c0001t0020g0006 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.496+4581G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141217285 | ||||||
| chr7:141217371
|
G | T | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.496+4667G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141217371 | ||||||
| chr7:141217385
|
G | C | 30 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0080others(27): Show | 30 | HG00544.hp1 HG01255.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.496+4681G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141217385 | ||||||
| chr7:141217511
|
G | T | 3 | a0001c0001t0035g0079a0001c0002t0017g0062a0001c0002t0026g0041 | 3 | HG02258.hp1 HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.496+4807G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141217511 | ||||||
| chr7:141217521
|
C | T | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.496+4817C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141217521 | ||||||
| chr7:141217523
|
G | A | 2 | a0001c0002t0015g0056a0001c0002t0040g0050 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.496+4819G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141217523 | ||||||
| chr7:141217556
|
A | G | 8 | a0001c0001t0002g0027a0001c0001t0006g0025a0001c0001t0008g0030others(5): Show | 8 | HG02486.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+4852A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141217556 | ||||||
| chr7:141217756
|
T | G | 24 | a0001c0001t0001g0080a0001c0001t0003g0007a0001c0001t0003g0020others(21): Show | 24 | HG00544.hp1 HG00544.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.496+5052T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141217756 | ||||||
| chr7:141218057
|
C | T | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.496+5353C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141218057 | ||||||
| chr7:141218509
|
T | C | 7 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(4): Show | 7 | HG01255.hp2 HG01952.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+5805T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141218509 | ||||||
| chr7:141218533
|
A | G | 59 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(56): Show | 59 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.496+5829A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141218533 | ||||||
| chr7:141218561
|
T | C | 59 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(56): Show | 59 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.496+5857T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141218561 | ||||||
| chr7:141218722
|
T | C | 59 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(56): Show | 59 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.496+6018T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141218722 | ||||||
| chr7:141218727
|
C | T | 5 | a0001c0001t0010g0021a0001c0001t0014g0033a0001c0001t0028g0022others(2): Show | 5 | HG01243.hp1 HG02922.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+6023C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141218727 | ||||||
| chr7:141218792
|
A | G | 59 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(56): Show | 59 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.496+6088A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141218792 | ||||||
| chr7:141218796
|
A | G | 59 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(56): Show | 59 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.496+6092A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141218796 | ||||||
| chr7:141218872
|
C | A | 58 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(55): Show | 58 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.496+6168C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141218872 | ||||||
| chr7:141218980
|
G | C | 68 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(65): Show | 68 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(65): Show |
intron_variant | MODIFIER | c.496+6276G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141218980 | ||||||
| chr7:141219019
|
T | C | 58 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(55): Show | 58 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.496+6315T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141219019 | ||||||
| chr7:141219373
|
A | C | 46 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(43): Show | 46 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.496+6669A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141219373 | ||||||
| chr7:141219398
|
C | T | 1 | a0001c0001t0004g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.496+6694C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141219398 | ||||||
| chr7:141219401
|
C | T | 3 | a0001c0001t0035g0079a0001c0002t0017g0062a0001c0002t0026g0041 | 3 | HG02258.hp1 HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.496+6697C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141219401 | ||||||
| chr7:141219435
|
C | T | 1 | a0001c0001t0020g0006 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.496+6731C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141219435 | ||||||
| chr7:141219479
|
A | G | 49 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(46): Show | 49 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.496+6775A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141219479 | ||||||
| chr7:141219538
|
A | G | 3 | a0001c0001t0005g0014a0001c0001t0023g0018a0001c0002t0040g0050 | 3 | HG03139.hp2 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.496+6834A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141219538 | ||||||
| chr7:141219721
|
G | A | 4 | a0001c0001t0002g0019a0001c0001t0004g0029a0001c0001t0033g0031others(1): Show | 4 | HG02630.hp1 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+7017G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141219721 | ||||||
| chr7:141219743
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.496+7039C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141219743 | ||||||
| chr7:141219750
|
T | A | 3 | a0001c0001t0005g0014a0001c0002t0015g0056a0001c0002t0040g0050 | 3 | HG03139.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.496+7046T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141219750 | ||||||
| chr7:141219780
|
A | G | 4 | a0001c0001t0002g0019a0001c0001t0004g0029a0001c0001t0033g0031others(1): Show | 4 | HG02630.hp1 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+7076A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141219780 | ||||||
| chr7:141219891
|
T | C | 6 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0001t0035g0079others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+7187T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141219891 | ||||||
| chr7:141220125
|
T | C | 59 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(56): Show | 59 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.496+7421T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141220125 | ||||||
| chr7:141220128
|
G | T | 59 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(56): Show | 59 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.496+7424G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141220128 | ||||||
| chr7:141220207
|
TGAGGCA | T | 59 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(56): Show | 59 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.496+7511_496+7516d others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141220207 | |||||
| chr7:141220227
|
T | C | 59 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(56): Show | 59 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.496+7523T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141220227 | ||||||
| chr7:141220268
|
G | A | 3 | a0001c0001t0005g0014a0001c0002t0015g0056a0001c0002t0040g0050 | 3 | HG03139.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.496+7564G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141220268 | ||||||
| chr7:141220311
|
AAAT | A | 4 | a0001c0001t0004g0024a0001c0001t0038g0034a0001c0002t0006g0040others(1): Show | 4 | HG01243.hp2 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+7655_496+7657d others(5): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141220311 | |||||
| chr7:141220311
|
AAATAAT | A | 11 | a0001c0001t0006g0025a0001c0001t0010g0021a0001c0001t0022g0013others(8): Show | 11 | HG01255.hp1 HG01261.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.496+7652_496+7657d others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141220311 | |||||
| chr7:141220311
|
AAATAATA others(2): Show |
A | 5 | a0001c0001t0001g0015a0001c0001t0002g0027a0001c0001t0006g0017others(2): Show | 5 | HG02258.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+7649_496+7657d others(11): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141220311 | |||||
| chr7:141220311
|
AAATAATA others(8): Show |
A | 8 | a0001c0001t0001g0012a0001c0001t0012g0036a0001c0001t0020g0006others(5): Show | 8 | HG01106.hp2 HG01255.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.496+7643_496+7657d others(17): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141220311 | |||||
| chr7:141220311
|
AAATAATA others(11): Show |
A | 4 | a0001c0001t0004g0023a0001c0001t0023g0018a0001c0002t0008g0003others(1): Show | 4 | HG01952.hp2 HG03579.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+7640_496+7657d others(20): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141220311 | |||||
| chr7:141220311
|
AAATAATA others(14): Show |
A | 36 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(33): Show | 36 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.496+7637_496+7657d others(23): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141220311 | |||||
| chr7:141220311
|
AAATAATA others(17): Show |
A | 6 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(3): Show | 6 | HG02109.hp2 HG02897.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+7634_496+7657d others(26): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141220311 | |||||
| chr7:141220347
|
TAATAATA others(7): Show |
T | 2 | a0001c0002t0001g0042a0001c0002t0026g0041 | 2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.496+7652_496+7665d others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141220347 | |||||
| chr7:141220350
|
TAATAATA others(4): Show |
T | 4 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0001t0035g0079others(1): Show | 4 | HG02258.hp1 HG02630.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+7655_496+7665d others(13): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141220350 | |||||
| chr7:141220359
|
T | A | 2 | a0001c0002t0007g0053a0001c0003t0019g0070 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.496+7655T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141220359 | ||||||
| chr7:141220367
|
T | A | 1 | a0001c0001t0004g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.496+7663T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141220367 | ||||||
| chr7:141220410
|
T | C | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+7706T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141220410 | ||||||
| chr7:141220520
|
G | A | 5 | a0001c0001t0002g0027a0001c0001t0006g0025a0001c0001t0025g0010others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+7816G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141220520 | ||||||
| chr7:141220588
|
C | T | 7 | a0001c0001t0022g0013a0001c0002t0001g0057a0001c0002t0007g0053others(4): Show | 7 | HG01243.hp2 HG01255.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+7884C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141220588 | ||||||
| chr7:141220761
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0002t0024g0002 | 3 | HG02897.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.496+8057C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141220761 | ||||||
| chr7:141220851
|
G | A | 29 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(26): Show | 29 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+8147G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141220851 | ||||||
| chr7:141220948
|
G | T | 4 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+8244G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141220948 | ||||||
| chr7:141220979
|
T | A | 1 | a0001c0003t0001g0074 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.496+8275T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141220979 | ||||||
| chr7:141221077
|
A | G | 6 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0001t0035g0079others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+8373A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141221077 | ||||||
| chr7:141221106
|
T | C | 3 | a0001c0001t0004g0024a0001c0001t0010g0021a0001c0001t0038g0034 | 3 | HG02922.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.496+8402T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141221106 | ||||||
| chr7:141221425
|
T | TG | 58 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(55): Show | 58 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.496+8722dupG | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141221425 | |||||
| chr7:141221451
|
A | G | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.496+8747A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141221451 | ||||||
| chr7:141221603
|
T | G | 58 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(55): Show | 58 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.496+8899T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141221603 | ||||||
| chr7:141221617
|
G | A | 50 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0002g0027others(47): Show | 50 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.496+8913G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141221617 | ||||||
| chr7:141221655
|
C | G | 58 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(55): Show | 58 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.496+8951C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141221655 | ||||||
| chr7:141221863
|
G | C | 53 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(50): Show | 53 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.496+9159G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141221863 | ||||||
| chr7:141222033
|
G | A | 39 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0002g0027others(36): Show | 39 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.496+9329G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141222033 | ||||||
| chr7:141222284
|
C | G | 1 | a0001c0001t0015g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.496+9580C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141222284 | ||||||
| chr7:141222437
|
C | T | 49 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(46): Show | 49 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.496+9733C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141222437 | ||||||
| chr7:141222441
|
T | C | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.496+9737T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141222441 | ||||||
| chr7:141222910
|
G | A | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.496+10206G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141222910 | ||||||
| chr7:141222924
|
T | A | 3 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0015g0028 | 3 | HG02897.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.496+10220T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141222924 | ||||||
| chr7:141223479
|
C | CTT | 4 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+10791_496+1079 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141223479 | |||||
| chr7:141223479
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0014g0039a0001c0002t0002g0043a0001c0002t0010g0066 | 3 | HG02615.hp2 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.496+10781_496+1079 others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141223479 | |||||
| chr7:141223479
|
C | CTTTTTTT others(6): Show |
4 | a0001c0001t0016g0037a0001c0001t0021g0077a0001c0001t0025g0010others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+10780_496+1079 others(17): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141223479 | |||||
| chr7:141223479
|
C | CTTTTTTT others(7): Show |
1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.496+10779_496+1079 others(18): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141223479 | |||||
| chr7:141223479
|
CT | C | 5 | a0001c0001t0001g0012a0001c0001t0004g0024a0001c0001t0010g0021others(2): Show | 5 | HG01106.hp2 HG01243.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+10792delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141223479 | |||||
| chr7:141223479
|
CTT | C | 7 | a0001c0001t0022g0013a0001c0001t0023g0018a0001c0002t0001g0057others(4): Show | 7 | HG01255.hp1 HG01261.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+10791_496+1079 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141223479 | |||||
| chr7:141223512
|
C | T | 6 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0021g0077others(3): Show | 6 | HG01891.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+10808C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141223512 | ||||||
| chr7:141223614
|
G | A | 20 | a0001c0001t0007g0011a0001c0001t0014g0039a0001c0001t0016g0037others(17): Show | 20 | HG00544.hp2 HG01243.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.496+10910G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141223614 | ||||||
| chr7:141223641
|
G | T | 7 | a0001c0001t0002g0027a0001c0001t0005g0014a0001c0001t0006g0025others(4): Show | 7 | HG02615.hp1 HG02630.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+10937G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141223641 | ||||||
| chr7:141223662
|
G | C | 1 | a0001c0001t0007g0011 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.496+10958G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141223662 | ||||||
| chr7:141223830
|
T | C | 50 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(47): Show | 50 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.496+11126T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141223830 | ||||||
| chr7:141223932
|
A | G | 78 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(75): Show | 78 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(75): Show |
intron_variant | MODIFIER | c.496+11228A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141223932 | ||||||
| chr7:141224028
|
G | A | 2 | a0001c0001t0016g0037a0001c0002t0002g0043 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.496+11324G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141224028 | ||||||
| chr7:141224034
|
C | G | 4 | a0001c0001t0004g0029a0001c0001t0008g0004a0001c0001t0033g0031others(1): Show | 4 | HG02630.hp1 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+11330C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141224034 | ||||||
| chr7:141224253
|
T | C | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+11549T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141224253 | ||||||
| chr7:141224388
|
A | C | 1 | a0001c0003t0018g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.496+11684A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141224388 | ||||||
| chr7:141224413
|
T | C | 2 | a0001c0002t0013g0059a0001c0002t0036g0069 | 2 | HG01255.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.496+11709T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141224413 | ||||||
| chr7:141224466
|
C | T | 40 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0002g0027others(37): Show | 40 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.496+11762C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141224466 | ||||||
| chr7:141224568
|
C | T | 2 | a0001c0001t0008g0004a0001c0002t0001g0042 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.496+11864C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141224568 | ||||||
| chr7:141224717
|
A | G | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.496+12013A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141224717 | ||||||
| chr7:141224761
|
C | T | 4 | a0001c0001t0004g0029a0001c0001t0008g0004a0001c0001t0033g0031others(1): Show | 4 | HG02630.hp1 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+12057C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141224761 | ||||||
| chr7:141224797
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0015g0028 | 3 | HG02897.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.496+12093A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141224797 | ||||||
| chr7:141224816
|
C | T | 7 | a0001c0001t0002g0027a0001c0001t0005g0014a0001c0001t0006g0025others(4): Show | 7 | HG02615.hp1 HG02630.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+12112C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141224816 | ||||||
| chr7:141225053
|
C | T | 12 | a0001c0001t0007g0011a0001c0001t0014g0039a0001c0001t0016g0037others(9): Show | 12 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.496+12349C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141225053 | ||||||
| chr7:141225116
|
A | G | 7 | a0001c0001t0022g0013a0001c0002t0001g0057a0001c0002t0007g0053others(4): Show | 7 | HG01243.hp2 HG01255.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+12412A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141225116 | ||||||
| chr7:141225271
|
A | G | 3 | a0001c0001t0035g0079a0001c0002t0017g0062a0001c0002t0026g0041 | 3 | HG02258.hp1 HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.496+12567A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141225271 | ||||||
| chr7:141225284
|
C | G | 1 | a0001c0002t0015g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.496+12580C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141225284 | ||||||
| chr7:141225422
|
A | G | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.496+12718A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141225422 | ||||||
| chr7:141225429
|
AT | A | 29 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0024others(26): Show | 29 | HG00544.hp2 HG01243.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.496+12734delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141225429 | |||||
| chr7:141225429
|
ATT | A | 11 | a0001c0001t0002g0027a0001c0001t0004g0029a0001c0001t0005g0014others(8): Show | 11 | HG02615.hp1 HG02630.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.496+12733_496+1273 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141225429 | |||||
| chr7:141225455
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.496+12751C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141225455 | ||||||
| chr7:141225468
|
C | T | 26 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0007g0011others(23): Show | 26 | HG00544.hp2 HG01243.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.496+12764C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141225468 | ||||||
| chr7:141225763
|
C | T | 53 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(50): Show | 53 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.496+13059C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141225763 | ||||||
| chr7:141225805
|
T | C | 7 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0029others(4): Show | 7 | HG02630.hp1 HG02897.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+13101T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141225805 | ||||||
| chr7:141225869
|
A | G | 7 | a0001c0001t0022g0013a0001c0002t0001g0057a0001c0002t0007g0053others(4): Show | 7 | HG01243.hp2 HG01255.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+13165A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141225869 | ||||||
| chr7:141225978
|
G | T | 4 | a0001c0001t0004g0029a0001c0001t0008g0004a0001c0001t0033g0031others(1): Show | 4 | HG02630.hp1 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+13274G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141225978 | ||||||
| chr7:141225986
|
A | G | 4 | a0001c0001t0004g0029a0001c0001t0008g0004a0001c0001t0033g0031others(1): Show | 4 | HG02630.hp1 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+13282A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141225986 | ||||||
| chr7:141226037
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+13333C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141226037 | ||||||
| chr7:141226065
|
G | A | 48 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(45): Show | 48 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.496+13361G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141226065 | ||||||
| chr7:141226194
|
C | T | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.496+13490C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141226194 | ||||||
| chr7:141226230
|
G | T | 2 | a0001c0001t0025g0010a0001c0004t0043g0032 | 2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.496+13526G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141226230 | ||||||
| chr7:141226397
|
C | T | 30 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(27): Show | 30 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.496+13693C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141226397 | ||||||
| chr7:141226584
|
G | A | 2 | a0001c0001t0004g0029a0001c0001t0033g0031 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.496+13880G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141226584 | ||||||
| chr7:141226716
|
G | A | 1 | a0001c0002t0001g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.496+14012G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141226716 | ||||||
| chr7:141226873
|
AAG | A | 51 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(48): Show | 51 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.496+14171_496+1417 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141226873 | |||||
| chr7:141226874
|
AG | A | 12 | a0001c0001t0001g0038a0001c0001t0004g0024a0001c0001t0010g0021others(9): Show | 12 | HG01891.hp2 HG01978.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.496+14171delG | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141226874 | ||||||
| chr7:141226875
|
G | A | 5 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0021g0077others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+14171G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141226875 | ||||||
| chr7:141226965
|
A | C | 11 | a0001c0001t0004g0024a0001c0001t0010g0021a0001c0001t0022g0013others(8): Show | 11 | HG01243.hp2 HG01255.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.496+14261A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141226965 | ||||||
| chr7:141227103
|
A | G | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+14399A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141227103 | ||||||
| chr7:141227224
|
G | A | 3 | a0001c0001t0004g0024a0001c0001t0010g0021a0001c0001t0038g0034 | 3 | HG02922.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.496+14520G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141227224 | ||||||
| chr7:141227413
|
A | G | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+14709A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141227413 | ||||||
| chr7:141227488
|
G | A | 11 | a0001c0001t0004g0024a0001c0001t0010g0021a0001c0001t0022g0013others(8): Show | 11 | HG01243.hp2 HG01255.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.496+14784G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141227488 | ||||||
| chr7:141227502
|
T | C | 15 | a0001c0001t0002g0027a0001c0001t0004g0029a0001c0001t0005g0014others(12): Show | 15 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+14798T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141227502 | ||||||
| chr7:141227536
|
A | G | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.496+14832A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141227536 | ||||||
| chr7:141227557
|
A | G | 2 | a0001c0001t0004g0029a0001c0001t0033g0031 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.496+14853A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141227557 | ||||||
| chr7:141227562
|
C | T | 3 | a0001c0001t0035g0079a0001c0002t0017g0062a0001c0002t0026g0041 | 3 | HG02258.hp1 HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.496+14858C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141227562 | ||||||
| chr7:141227795
|
C | T | 3 | a0001c0001t0004g0024a0001c0001t0010g0021a0001c0001t0038g0034 | 3 | HG02922.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.496+15091C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141227795 | ||||||
| chr7:141228039
|
T | TAC | 6 | a0001c0001t0005g0008a0001c0001t0035g0079a0001c0001t0044g0001others(3): Show | 6 | HG01256.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+15353_496+1535 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141228039 | |||||
| chr7:141228040
|
A | G | 7 | a0001c0001t0002g0027a0001c0001t0005g0014a0001c0001t0006g0025others(4): Show | 7 | HG02615.hp1 HG02630.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+15336A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141228040 | ||||||
| chr7:141228041
|
C | T | 7 | a0001c0001t0002g0027a0001c0001t0005g0014a0001c0001t0006g0025others(4): Show | 7 | HG02615.hp1 HG02630.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+15337C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141228041 | ||||||
| chr7:141228142
|
T | C | 26 | a0001c0001t0002g0027a0001c0001t0004g0024a0001c0001t0004g0029others(23): Show | 26 | HG00544.hp2 HG01243.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.496+15438T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141228142 | ||||||
| chr7:141228430
|
G | A | 4 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+15726G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141228430 | ||||||
| chr7:141228619
|
G | A | 4 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+15915G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141228619 | ||||||
| chr7:141229013
|
C | CTTTTT | 10 | a0001c0001t0002g0027a0001c0001t0004g0029a0001c0001t0005g0014others(7): Show | 10 | HG02615.hp1 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+16327_496+1633 others(9): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141229013 | |||||
| chr7:141229013
|
CT | C | 47 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(44): Show | 47 | HG01106.hp1 HG01106.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.496+16331delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141229013 | |||||
| chr7:141229013
|
CTT | C | 16 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(13): Show | 16 | HG00544.hp1 HG01243.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.496+16330_496+1633 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141229013 | |||||
| chr7:141229013
|
CTTTT | C | 4 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+16328_496+1633 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141229013 | |||||
| chr7:141229100
|
G | GGT | 15 | a0001c0001t0002g0027a0001c0001t0005g0014a0001c0001t0006g0025others(12): Show | 15 | HG01891.hp1 HG01891.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.496+16426_496+1642 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141229100 | |||||
| chr7:141229100
|
G | GGTGT | 4 | a0001c0001t0006g0017a0001c0002t0013g0059a0001c0002t0036g0069others(1): Show | 4 | HG01255.hp2 HG01256.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+16424_496+1642 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141229100 | |||||
| chr7:141229100
|
G | GGTGTGT | 3 | a0001c0001t0004g0024a0001c0001t0022g0013a0001c0001t0038g0034 | 3 | HG01261.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.496+16422_496+1642 others(10): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141229100 | |||||
| chr7:141229100
|
G | GGTGTGTG others(3): Show |
6 | a0001c0001t0023g0018a0001c0002t0001g0057a0001c0002t0007g0053others(3): Show | 6 | HG01243.hp2 HG01255.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+16418_496+1642 others(14): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141229100 | |||||
| chr7:141229100
|
G | GGTGTGTG others(5): Show |
1 | a0001c0003t0019g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.496+16416_496+1642 others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141229100 | |||||
| chr7:141229100
|
G | GGTGTGTG others(7): Show |
3 | a0001c0001t0008g0004a0001c0001t0033g0031a0001c0002t0001g0042 | 3 | HG02630.hp1 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.496+16414_496+1642 others(18): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141229100 | |||||
| chr7:141229100
|
G | GGTGTGTG others(11): Show |
1 | a0001c0001t0004g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.496+16410_496+1642 others(22): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141229100 | |||||
| chr7:141229100
|
GGT | G | 2 | a0001c0001t0007g0011a0001c0002t0013g0047 | 2 | HG00544.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.496+16426_496+1642 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141229100 | |||||
| chr7:141229100
|
GGTGTGTG others(3): Show |
G | 2 | a0001c0001t0034g0009a0001c0002t0009g0060 | 2 | HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.496+16418_496+1642 others(14): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141229100 | |||||
| chr7:141229125
|
G | C | 29 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(26): Show | 29 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.496+16421G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141229125 | ||||||
| chr7:141229276
|
C | T | 3 | a0001c0001t0004g0024a0001c0001t0010g0021a0001c0001t0038g0034 | 3 | HG02922.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.496+16572C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141229276 | ||||||
| chr7:141229805
|
T | A | 4 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+17101T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141229805 | ||||||
| chr7:141230014
|
C | T | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.496+17310C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141230014 | ||||||
| chr7:141230038
|
T | C | 14 | a0001c0001t0002g0027a0001c0001t0004g0029a0001c0001t0005g0014others(11): Show | 14 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.496+17334T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141230038 | ||||||
| chr7:141230212
|
T | G | 2 | a0001c0001t0003g0020a0001c0001t0009g0078 | 2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.496+17508T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141230212 | ||||||
| chr7:141230499
|
T | C | 6 | a0001c0001t0002g0027a0001c0001t0005g0014a0001c0001t0006g0025others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+17795T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141230499 | ||||||
| chr7:141231033
|
C | T | 4 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+18329C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141231033 | ||||||
| chr7:141231094
|
G | A | 6 | a0001c0001t0002g0027a0001c0001t0005g0014a0001c0001t0006g0025others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+18390G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141231094 | ||||||
| chr7:141231181
|
G | A | 4 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+18477G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141231181 | ||||||
| chr7:141231310
|
G | GAA | 4 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+18607_496+1860 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141231310 | |||||
| chr7:141231313
|
G | A | 4 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+18609G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141231313 | ||||||
| chr7:141231313
|
G | GA | 43 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(40): Show | 43 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.496+18621dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141231313 | |||||
| chr7:141231403
|
C | T | 8 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0021g0077others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+18699C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141231403 | ||||||
| chr7:141231591
|
C | T | 8 | a0001c0001t0022g0013a0001c0001t0023g0018a0001c0002t0001g0057others(5): Show | 8 | HG01243.hp2 HG01255.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.496+18887C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141231591 | ||||||
| chr7:141231957
|
C | T | 1 | a0001c0001t0012g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.496+19253C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141231957 | ||||||
| chr7:141232020
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+19316C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141232020 | ||||||
| chr7:141232286
|
C | T | 4 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+19582C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141232286 | ||||||
| chr7:141234113
|
A | C | 24 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(21): Show | 24 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.496+21409A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141234113 | ||||||
| chr7:141234325
|
G | A | 5 | a0001c0001t0003g0020a0001c0001t0009g0078a0001c0002t0015g0056others(2): Show | 5 | HG01261.hp2 HG02647.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+21621G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141234325 | ||||||
| chr7:141234737
|
A | C | 1 | a0001c0001t0033g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.496+22033A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141234737 | ||||||
| chr7:141235399
|
G | A | 1 | a0001c0001t0009g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.496+22695G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141235399 | ||||||
| chr7:141235454
|
G | A | 8 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0021g0077others(5): Show | 8 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+22750G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141235454 | ||||||
| chr7:141235850
|
T | G | 1 | a0001c0002t0010g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.496+23146T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141235850 | ||||||
| chr7:141235878
|
G | A | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.496+23174G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141235878 | ||||||
| chr7:141235985
|
A | T | 3 | a0001c0001t0035g0079a0001c0002t0017g0062a0001c0002t0026g0041 | 3 | HG02258.hp1 HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.496+23281A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141235985 | ||||||
| chr7:141236288
|
C | T | 70 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(67): Show | 70 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(67): Show |
intron_variant | MODIFIER | c.496+23584C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141236288 | ||||||
| chr7:141236352
|
G | A | 29 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(26): Show | 29 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.496+23648G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141236352 | ||||||
| chr7:141236538
|
C | A | 2 | a0001c0001t0004g0029a0001c0001t0033g0031 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.496+23834C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141236538 | ||||||
| chr7:141236668
|
C | T | 70 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(67): Show | 70 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(67): Show |
intron_variant | MODIFIER | c.496+23964C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141236668 | ||||||
| chr7:141236693
|
A | C | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+23989A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141236693 | ||||||
| chr7:141236761
|
A | G | 70 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(67): Show | 70 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(67): Show |
intron_variant | MODIFIER | c.496+24057A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141236761 | ||||||
| chr7:141236910
|
C | T | 4 | a0001c0001t0004g0024a0001c0001t0005g0008a0001c0001t0038g0034others(1): Show | 4 | HG02922.hp1 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+24206C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141236910 | ||||||
| chr7:141237086
|
A | G | 2 | a0001c0002t0001g0064a0001c0002t0027g0051 | 2 | HG02486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.496+24382A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141237086 | ||||||
| chr7:141237278
|
T | C | 27 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(24): Show | 27 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.496+24574T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141237278 | ||||||
| chr7:141237355
|
GGTAA | G | 4 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+24654_496+2465 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141237355 | |||||
| chr7:141237495
|
G | A | 9 | a0001c0001t0004g0024a0001c0001t0005g0008a0001c0001t0007g0011others(6): Show | 9 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.496+24791G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141237495 | ||||||
| chr7:141237596
|
T | G | 3 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0015g0028 | 3 | HG02897.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.496+24892T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141237596 | ||||||
| chr7:141237695
|
A | C | 1 | a0001c0002t0013g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.496+24991A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141237695 | ||||||
| chr7:141238022
|
T | TA | 4 | a0001c0001t0021g0077a0001c0001t0035g0079a0001c0002t0017g0062others(1): Show | 4 | HG02258.hp1 HG02572.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+25337dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141238022 | |||||
| chr7:141238022
|
TA | T | 12 | a0001c0001t0007g0011a0001c0001t0022g0013a0001c0002t0001g0057others(9): Show | 12 | HG00544.hp2 HG01243.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.496+25337delA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141238022 | |||||
| chr7:141238041
|
A | G | 26 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(23): Show | 26 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.496+25337A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141238041 | ||||||
| chr7:141238053
|
A | G | 5 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0021g0077others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+25349A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141238053 | ||||||
| chr7:141238101
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.496+25397C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141238101 | ||||||
| chr7:141238121
|
G | A | 7 | a0001c0001t0022g0013a0001c0002t0001g0057a0001c0002t0007g0053others(4): Show | 7 | HG01243.hp2 HG01255.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+25417G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141238121 | ||||||
| chr7:141238162
|
G | C | 1 | a0001c0001t0015g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.496+25458G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141238162 | ||||||
| chr7:141238743
|
C | T | 63 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(60): Show | 63 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.496+26039C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141238743 | ||||||
| chr7:141238751
|
G | A | 63 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(60): Show | 63 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.496+26047G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141238751 | ||||||
| chr7:141239065
|
G | T | 8 | a0001c0001t0008g0004a0001c0001t0022g0013a0001c0002t0001g0057others(5): Show | 8 | HG01243.hp2 HG01255.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.496+26361G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141239065 | ||||||
| chr7:141239332
|
G | A | 60 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(57): Show | 60 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(57): Show |
intron_variant | MODIFIER | c.496+26628G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141239332 | ||||||
| chr7:141239638
|
G | A | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.496+26934G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141239638 | ||||||
| chr7:141239836
|
TG | T | 11 | a0001c0001t0022g0013a0001c0001t0023g0018a0001c0001t0035g0079others(8): Show | 11 | HG01243.hp2 HG01255.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.496+27134delG | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141239836 | |||||
| chr7:141240056
|
C | T | 1 | a0001c0002t0041g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.496+27352C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141240056 | ||||||
| chr7:141240115
|
A | G | 11 | a0001c0001t0022g0013a0001c0001t0023g0018a0001c0001t0035g0079others(8): Show | 11 | HG01243.hp2 HG01255.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.496+27411A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141240115 | ||||||
| chr7:141240494
|
A | G | 1 | a0001c0003t0018g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.496+27790A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141240494 | ||||||
| chr7:141240637
|
C | T | 3 | a0001c0001t0004g0024a0001c0001t0038g0034a0001c0002t0003g0052 | 3 | HG01891.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.496+27933C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141240637 | ||||||
| chr7:141240832
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(5): Show | 8 | HG01952.hp1 HG01978.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+28128C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141240832 | ||||||
| chr7:141240864
|
T | A | 69 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(66): Show | 69 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(66): Show |
intron_variant | MODIFIER | c.496+28160T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141240864 | ||||||
| chr7:141240996
|
CT | C | 48 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0020others(45): Show | 48 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.496+28307delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141240996 | |||||
| chr7:141240996
|
CTT | C | 17 | a0001c0001t0001g0015a0001c0001t0003g0007a0001c0001t0004g0024others(14): Show | 17 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.496+28306_496+2830 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141240996 | |||||
| chr7:141241022
|
C | A | 1 | a0001c0001t0015g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.496+28318C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141241022 | ||||||
| chr7:141241043
|
G | A | 45 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(42): Show | 45 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.496+28339G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141241043 | ||||||
| chr7:141241057
|
T | C | 1 | a0001c0002t0013g0059 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.496+28353T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141241057 | ||||||
| chr7:141241143
|
GT | G | 72 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(69): Show | 72 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(69): Show |
intron_variant | MODIFIER | c.496+28450delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141241143 | |||||
| chr7:141241278
|
C | T | 69 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(66): Show | 69 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(66): Show |
intron_variant | MODIFIER | c.496+28574C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141241278 | ||||||
| chr7:141241522
|
A | G | 2 | a0001c0001t0006g0025a0001c0002t0006g0040 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.496+28818A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141241522 | ||||||
| chr7:141241586
|
G | A | 8 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(5): Show | 8 | HG01952.hp1 HG01978.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+28882G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141241586 | ||||||
| chr7:141241590
|
C | CA | 5 | a0001c0001t0001g0012a0001c0001t0004g0029a0001c0001t0033g0031others(2): Show | 5 | HG01106.hp2 HG02027.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+28909dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141241590 | |||||
| chr7:141241590
|
C | CAA | 12 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0007g0011others(9): Show | 12 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.496+28908_496+2890 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141241590 | |||||
| chr7:141241590
|
CA | C | 14 | a0001c0001t0004g0024a0001c0001t0022g0013a0001c0001t0023g0018others(11): Show | 14 | HG01243.hp2 HG01255.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.496+28909delA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141241590 | |||||
| chr7:141241750
|
A | G | 4 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+29046A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141241750 | ||||||
| chr7:141242148
|
CTT | C | 2 | a0001c0001t0014g0033a0001c0001t0028g0022 | 2 | HG01243.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.496+29448_496+2944 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141242148 | |||||
| chr7:141242211
|
CCAAA | C | 26 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(23): Show | 26 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.496+29512_496+2951 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141242211 | |||||
| chr7:141242373
|
C | CTTTTTTT others(1936): Show |
2 | a0001c0001t0001g0035a0001c0001t0015g0028 | 2 | HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.496+29673_496+2967 others(1947): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141242373 | |||||
| chr7:141242373
|
C | CTTTTTTT others(1937): Show |
1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.496+29673_496+2967 others(1948): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141242373 | |||||
| chr7:141242477
|
AGT | A | 12 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0008g0030others(9): Show | 12 | HG01952.hp1 HG01978.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.496+29804_496+2980 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141242477 | |||||
| chr7:141242477
|
AGTGT | A | 40 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0003g0007others(37): Show | 40 | HG01106.hp1 HG01243.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.496+29802_496+2980 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141242477 | |||||
| chr7:141242477
|
AGTGTGT | A | 12 | a0001c0001t0001g0080a0001c0001t0002g0019a0001c0001t0007g0011others(9): Show | 12 | HG00544.hp1 HG00544.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.496+29800_496+2980 others(10): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141242477 | |||||
| chr7:141242541
|
C | CT | 5 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(2): Show | 5 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+29855dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141242541 | |||||
| chr7:141242541
|
CT | C | 62 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(59): Show | 62 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.496+29855delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141242541 | |||||
| chr7:141242564
|
C | T | 1 | a0001c0001t0038g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.496+29860C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141242564 | ||||||
| chr7:141242701
|
A | G | 4 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0002t0002g0043others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+29997A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141242701 | ||||||
| chr7:141242753
|
G | C | 1 | a0001c0001t0007g0011 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.496+30049G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141242753 | ||||||
| chr7:141243198
|
T | C | 72 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(69): Show | 72 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(69): Show |
intron_variant | MODIFIER | c.496+30494T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141243198 | ||||||
| chr7:141243272
|
T | C | 50 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(47): Show | 50 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.496+30568T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141243272 | ||||||
| chr7:141243378
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0015g0028 | 3 | HG02897.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.496+30674G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141243378 | ||||||
| chr7:141243388
|
C | T | 27 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(24): Show | 27 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.496+30684C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141243388 | ||||||
| chr7:141243423
|
C | CAG | 2 | a0001c0002t0001g0048a0001c0002t0001g0065 | 2 | HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.496+30721_496+3072 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141243423 | |||||
| chr7:141244137
|
C | T | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.496+31433C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141244137 | ||||||
| chr7:141244240
|
T | C | 4 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0002t0002g0043others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+31536T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141244240 | ||||||
| chr7:141244247
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(1): Show | 4 | HG02897.hp2 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+31543C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141244247 | ||||||
| chr7:141244297
|
A | G | 4 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(1): Show | 4 | HG02897.hp2 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+31593A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141244297 | ||||||
| chr7:141244812
|
G | T | 37 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(34): Show | 37 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.496+32108G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141244812 | ||||||
| chr7:141244860
|
A | G | 5 | a0001c0001t0004g0029a0001c0001t0008g0004a0001c0001t0008g0030others(2): Show | 5 | HG01884.hp2 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+32156A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141244860 | ||||||
| chr7:141244886
|
C | T | 29 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0024others(26): Show | 29 | HG00544.hp2 HG01243.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.496+32182C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141244886 | ||||||
| chr7:141245005
|
C | T | 3 | a0001c0001t0004g0024a0001c0001t0005g0008a0001c0002t0003g0052 | 3 | HG01891.hp2 HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.496+32301C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141245005 | ||||||
| chr7:141245104
|
A | G | 1 | a0001c0002t0012g0045 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.496+32400A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141245104 | ||||||
| chr7:141245170
|
C | CA | 6 | a0001c0001t0001g0080a0001c0001t0004g0023a0001c0002t0001g0064others(3): Show | 6 | HG00544.hp1 HG00544.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+32506dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141245170 | |||||
| chr7:141245170
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0029g0026 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.496+32495_496+3250 others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141245170 | |||||
| chr7:141245170
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0028g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.496+32494_496+3250 others(17): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141245170 | |||||
| chr7:141245170
|
CA | C | 16 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(13): Show | 16 | HG01256.hp2 HG02083.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.496+32506delA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141245170 | |||||
| chr7:141245170
|
CAAA | C | 5 | a0001c0001t0004g0024a0001c0002t0007g0053a0001c0002t0026g0041others(2): Show | 5 | HG01255.hp1 HG01256.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+32504_496+3250 others(7): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141245170 | |||||
| chr7:141245170
|
CAAAAA | C | 4 | a0001c0001t0022g0013a0001c0001t0035g0079a0001c0002t0001g0057others(1): Show | 4 | HG01261.hp1 HG01978.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+32502_496+3250 others(9): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141245170 | |||||
| chr7:141245170
|
CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0001g0012a0001c0001t0005g0008 | 2 | HG01106.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.496+32488_496+3250 others(23): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141245170 | |||||
| chr7:141245170
|
CAAAAAAA others(14): Show |
C | 1 | a0001c0001t0015g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.496+32486_496+3250 others(25): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141245170 | |||||
| chr7:141245170
|
CAAAAAAA others(17): Show |
C | 10 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(7): Show | 10 | HG01952.hp1 HG01978.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+32483_496+3250 others(28): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141245170 | |||||
| chr7:141245192
|
AAAAAAAA others(12): Show |
A | 4 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0002t0002g0043others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+32491_496+3250 others(23): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141245192 | |||||
| chr7:141245449
|
A | G | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.496+32745A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141245449 | ||||||
| chr7:141245504
|
C | T | 39 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(36): Show | 39 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.496+32800C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141245504 | ||||||
| chr7:141245796
|
C | G | 1 | a0001c0002t0001g0057 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.496+33092C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141245796 | ||||||
| chr7:141245999
|
A | AT | 4 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0002t0002g0043others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+33306dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141245999 | |||||
| chr7:141246154
|
C | T | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.496+33450C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141246154 | ||||||
| chr7:141246454
|
A | G | 39 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(36): Show | 39 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.496+33750A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141246454 | ||||||
| chr7:141246510
|
A | G | 9 | a0001c0001t0004g0024a0001c0001t0007g0011a0001c0001t0035g0079others(6): Show | 9 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.496+33806A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141246510 | ||||||
| chr7:141246693
|
G | A | 39 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(36): Show | 39 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.496+33989G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141246693 | ||||||
| chr7:141246780
|
A | G | 41 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(38): Show | 41 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.496+34076A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141246780 | ||||||
| chr7:141246833
|
C | T | 39 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(36): Show | 39 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.496+34129C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141246833 | ||||||
| chr7:141246846
|
G | A | 2 | a0001c0001t0016g0037a0001c0002t0002g0043 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.496+34142G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141246846 | ||||||
| chr7:141247110
|
G | A | 10 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(7): Show | 10 | HG01952.hp1 HG01978.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+34406G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141247110 | ||||||
| chr7:141247119
|
T | C | 39 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(36): Show | 39 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.496+34415T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141247119 | ||||||
| chr7:141247154
|
T | C | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.496+34450T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141247154 | ||||||
| chr7:141247187
|
A | C | 26 | a0001c0001t0003g0007a0001c0001t0004g0023a0001c0001t0004g0024others(23): Show | 26 | HG00544.hp2 HG01243.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.496+34483A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141247187 | ||||||
| chr7:141247204
|
T | TAC | 4 | a0001c0001t0004g0024a0001c0001t0005g0008a0001c0002t0003g0052others(1): Show | 4 | HG01891.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+34524_496+3452 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141247204 | |||||
| chr7:141247204
|
T | TACAC | 10 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0029others(7): Show | 10 | HG01891.hp1 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.496+34522_496+3452 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141247204 | |||||
| chr7:141247204
|
TAC | T | 3 | a0001c0001t0035g0079a0001c0002t0017g0062a0001c0003t0019g0070 | 3 | HG01884.hp1 HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.496+34524_496+3452 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141247204 | |||||
| chr7:141247204
|
TACAC | T | 39 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(36): Show | 39 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.496+34522_496+3452 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141247204 | |||||
| chr7:141247986
|
C | G | 39 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(36): Show | 39 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.496+35282C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141247986 | ||||||
| chr7:141248037
|
CT | C | 39 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(36): Show | 39 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.496+35344delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141248037 | |||||
| chr7:141248071
|
G | T | 39 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(36): Show | 39 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.496+35367G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141248071 | ||||||
| chr7:141248190
|
A | C | 39 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(36): Show | 39 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.496+35486A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141248190 | ||||||
| chr7:141248326
|
G | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+35622G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141248326 | ||||||
| chr7:141248344
|
G | A | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.496+35640G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141248344 | ||||||
| chr7:141248376
|
A | G | 39 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(36): Show | 39 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.496+35672A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141248376 | ||||||
| chr7:141248539
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.496+35835C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141248539 | ||||||
| chr7:141248639
|
G | T | 50 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(47): Show | 50 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.496+35935G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141248639 | ||||||
| chr7:141249157
|
A | G | 39 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(36): Show | 39 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.496+36453A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141249157 | ||||||
| chr7:141249245
|
T | C | 2 | a0001c0001t0004g0024a0001c0002t0003g0052 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.496+36541T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141249245 | ||||||
| chr7:141249277
|
G | T | 39 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(36): Show | 39 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.496+36573G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141249277 | ||||||
| chr7:141249282
|
C | G | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.496+36578C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141249282 | ||||||
| chr7:141249333
|
C | A | 39 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(36): Show | 39 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.496+36629C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141249333 | ||||||
| chr7:141249536
|
T | A | 1 | a0001c0001t0004g0023 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.496+36832T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141249536 | ||||||
| chr7:141249659
|
C | CCTTGTG | 61 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(58): Show | 61 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.496+36955_496+3695 others(10): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141249659 | ||||||
| chr7:141249982
|
A | G | 29 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(26): Show | 29 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.496+37278A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141249982 | ||||||
| chr7:141249984
|
C | T | 1 | a0001c0001t0038g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.496+37280C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141249984 | ||||||
| chr7:141250073
|
T | C | 1 | a0001c0001t0011g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.496+37369T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141250073 | ||||||
| chr7:141250276
|
A | C | 1 | a0001c0002t0036g0069 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.496+37572A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141250276 | ||||||
| chr7:141250335
|
A | T | 3 | a0001c0001t0034g0009a0001c0002t0009g0060a0001c0002t0015g0056 | 3 | HG03130.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.496+37631A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141250335 | ||||||
| chr7:141250582
|
A | ATGTTCTC others(23): Show |
1 | a0001c0002t0041g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.496+37881_496+3791 others(34): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141250582 | |||||
| chr7:141250618
|
A | G | 77 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(74): Show | 77 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(74): Show |
intron_variant | MODIFIER | c.496+37914A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141250618 | ||||||
| chr7:141250643
|
C | T | 1 | a0001c0001t0006g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.496+37939C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141250643 | ||||||
| chr7:141251079
|
A | G | 29 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(26): Show | 29 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.496+38375A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141251079 | ||||||
| chr7:141251128
|
A | T | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.496+38424A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141251128 | ||||||
| chr7:141251591
|
A | C | 14 | a0001c0001t0007g0011a0001c0001t0022g0013a0001c0001t0035g0079others(11): Show | 14 | HG00544.hp2 HG01243.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.496+38887A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141251591 | ||||||
| chr7:141251825
|
C | T | 1 | a0001c0002t0003g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.496+39121C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141251825 | ||||||
| chr7:141251927
|
G | A | 2 | a0001c0001t0005g0014a0001c0002t0040g0050 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.496+39223G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141251927 | ||||||
| chr7:141252047
|
C | T | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+39343C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141252047 | ||||||
| chr7:141252348
|
C | T | 1 | a0001c0002t0037g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.496+39644C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141252348 | ||||||
| chr7:141252430
|
G | A | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.496+39726G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141252430 | ||||||
| chr7:141252476
|
T | C | 2 | a0001c0001t0015g0028a0001c0001t0025g0010 | 2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.496+39772T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141252476 | ||||||
| chr7:141252480
|
G | T | 6 | a0001c0001t0004g0029a0001c0001t0005g0008a0001c0001t0008g0004others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+39776G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141252480 | ||||||
| chr7:141252483
|
G | A | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+39779G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141252483 | ||||||
| chr7:141252630
|
G | T | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.496+39926G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141252630 | ||||||
| chr7:141253164
|
G | A | 6 | a0001c0001t0004g0029a0001c0001t0005g0008a0001c0001t0008g0004others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+40460G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141253164 | ||||||
| chr7:141253280
|
T | C | 2 | a0001c0001t0004g0024a0001c0002t0003g0052 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.496+40576T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141253280 | ||||||
| chr7:141253543
|
T | TC | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.496+40840dupC | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141253543 | |||||
| chr7:141253544
|
C | CT | 35 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(32): Show | 35 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.496+40863dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141253544 | |||||
| chr7:141253544
|
C | CTT | 5 | a0001c0001t0010g0021a0001c0001t0016g0037a0001c0002t0002g0043others(2): Show | 5 | HG01891.hp1 HG02572.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+40862_496+4086 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141253544 | |||||
| chr7:141253854
|
C | G | 2 | a0001c0002t0007g0053a0001c0003t0019g0070 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.496+41150C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141253854 | ||||||
| chr7:141253881
|
T | A | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+41177T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141253881 | ||||||
| chr7:141254515
|
C | T | 6 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0035g0079others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+41811C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141254515 | ||||||
| chr7:141254530
|
T | C | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+41826T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141254530 | ||||||
| chr7:141254642
|
C | T | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+41938C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141254642 | ||||||
| chr7:141254717
|
G | T | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+42013G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141254717 | ||||||
| chr7:141254813
|
G | A | 54 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0080others(51): Show | 54 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.496+42109G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141254813 | ||||||
| chr7:141255085
|
G | A | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+42381G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141255085 | ||||||
| chr7:141255339
|
T | C | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+42635T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141255339 | ||||||
| chr7:141255648
|
G | GT | 7 | a0001c0001t0022g0013a0001c0002t0001g0057a0001c0002t0007g0053others(4): Show | 7 | HG01243.hp2 HG01255.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+42954dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141255648 | |||||
| chr7:141255648
|
GT | G | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+42954delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141255648 | |||||
| chr7:141255801
|
C | T | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.496+43097C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141255801 | ||||||
| chr7:141255952
|
G | A | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+43248G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141255952 | ||||||
| chr7:141256031
|
CATCT | C | 5 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(2): Show | 5 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+43328_496+4333 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141256031 | ||||||
| chr7:141256052
|
ATCCATCC others(1): Show |
A | 2 | a0001c0001t0035g0079a0001c0002t0017g0062 | 2 | HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.496+43364_496+4337 others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141256052 | |||||
| chr7:141256259
|
A | C | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+43555A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141256259 | ||||||
| chr7:141256364
|
G | A | 4 | a0001c0001t0010g0021a0001c0001t0015g0028a0001c0001t0023g0018others(1): Show | 4 | HG02486.hp1 HG03516.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+43660G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141256364 | ||||||
| chr7:141256486
|
C | T | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.496+43782C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141256486 | ||||||
| chr7:141256682
|
T | C | 1 | a0001c0002t0001g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.496+43978T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141256682 | ||||||
| chr7:141256724
|
G | A | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.496+44020G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141256724 | ||||||
| chr7:141256828
|
G | A | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+44124G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141256828 | ||||||
| chr7:141256843
|
A | G | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+44139A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141256843 | ||||||
| chr7:141256873
|
A | G | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+44169A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141256873 | ||||||
| chr7:141257023
|
C | G | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+44319C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141257023 | ||||||
| chr7:141257499
|
C | G | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+44795C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141257499 | ||||||
| chr7:141257499
|
C | T | 7 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0035g0079others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+44795C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141257499 | ||||||
| chr7:141257708
|
C | T | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+45004C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141257708 | ||||||
| chr7:141257724
|
C | A | 10 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(7): Show | 10 | HG01952.hp1 HG01978.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+45020C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141257724 | ||||||
| chr7:141257920
|
CCTTA | C | 6 | a0001c0001t0004g0029a0001c0001t0005g0008a0001c0001t0008g0004others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+45220_496+4522 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141257920 | |||||
| chr7:141258042
|
A | G | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+45338A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141258042 | ||||||
| chr7:141258161
|
C | CAT | 3 | a0001c0001t0007g0011a0001c0002t0013g0059a0001c0002t0036g0069 | 3 | HG01255.hp2 HG01256.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.496+45478_496+4547 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141258161 | |||||
| chr7:141258161
|
CAT | C | 15 | a0001c0001t0001g0012a0001c0001t0002g0027a0001c0001t0005g0014others(12): Show | 15 | HG01106.hp2 HG01891.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.496+45478_496+4547 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141258161 | |||||
| chr7:141258161
|
CATAT | C | 53 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(50): Show | 53 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.496+45476_496+4547 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141258161 | |||||
| chr7:141258199
|
A | G | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.496+45495A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141258199 | ||||||
| chr7:141258246
|
A | C | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+45542A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141258246 | ||||||
| chr7:141258482
|
CT | C | 9 | a0001c0001t0001g0012a0001c0001t0002g0027a0001c0001t0005g0014others(6): Show | 9 | HG01106.hp2 HG02602.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.496+45782delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141258482 | |||||
| chr7:141258571
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.496+45867C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141258571 | ||||||
| chr7:141258572
|
A | T | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.496+45868A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141258572 | ||||||
| chr7:141258574
|
G | T | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.496+45870G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141258574 | ||||||
| chr7:141258575
|
TTACAGCC others(1): Show |
T | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.496+45872_496+4587 others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141258575 | ||||||
| chr7:141258584
|
A | C | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.496+45880A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141258584 | ||||||
| chr7:141258645
|
C | T | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.496+45941C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141258645 | ||||||
| chr7:141258740
|
C | A | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+46036C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141258740 | ||||||
| chr7:141258787
|
C | T | 2 | a0001c0001t0005g0014a0001c0002t0040g0050 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.496+46083C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141258787 | ||||||
| chr7:141258788
|
G | A | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+46084G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141258788 | ||||||
| chr7:141258852
|
A | G | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+46148A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141258852 | ||||||
| chr7:141258858
|
G | A | 1 | a0001c0002t0005g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.496+46154G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141258858 | ||||||
| chr7:141258922
|
A | G | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+46218A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141258922 | ||||||
| chr7:141259492
|
A | G | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.496+46788A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141259492 | ||||||
| chr7:141259576
|
A | T | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+46872A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141259576 | ||||||
| chr7:141259887
|
C | T | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.496+47183C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141259887 | ||||||
| chr7:141260207
|
G | A | 68 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(65): Show | 68 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(65): Show |
intron_variant | MODIFIER | c.496+47503G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141260207 | ||||||
| chr7:141260411
|
AT | A | 68 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(65): Show | 68 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(65): Show |
intron_variant | MODIFIER | c.496+47716delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141260411 | |||||
| chr7:141260486
|
C | A | 6 | a0001c0001t0004g0029a0001c0001t0005g0008a0001c0001t0008g0004others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+47782C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141260486 | ||||||
| chr7:141260562
|
A | G | 2 | a0001c0001t0004g0024a0001c0002t0003g0052 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.496+47858A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141260562 | ||||||
| chr7:141260844
|
T | G | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.496+48140T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141260844 | ||||||
| chr7:141261035
|
A | C | 52 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0080others(49): Show | 52 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.496+48331A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141261035 | ||||||
| chr7:141261416
|
C | A | 10 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(7): Show | 10 | HG01952.hp1 HG01978.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+48712C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141261416 | ||||||
| chr7:141261705
|
G | A | 6 | a0001c0001t0004g0029a0001c0001t0005g0008a0001c0001t0008g0004others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+49001G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141261705 | ||||||
| chr7:141262099
|
A | C | 63 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(60): Show | 63 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.496+49395A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141262099 | ||||||
| chr7:141262124
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.496+49420C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141262124 | ||||||
| chr7:141262245
|
G | T | 2 | a0001c0001t0004g0024a0001c0002t0003g0052 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.496+49541G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141262245 | ||||||
| chr7:141262465
|
A | C | 71 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(68): Show | 71 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(68): Show |
intron_variant | MODIFIER | c.496+49761A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141262465 | ||||||
| chr7:141262474
|
A | AAT | 8 | a0001c0001t0004g0024a0001c0001t0004g0029a0001c0001t0008g0030others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.496+49799_496+4980 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141262474 | |||||
| chr7:141262474
|
A | AATATATA others(7): Show |
1 | a0001c0002t0006g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.496+49787_496+4980 others(18): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141262474 | |||||
| chr7:141262474
|
A | AATATATA others(9): Show |
2 | a0001c0001t0002g0027a0001c0001t0006g0025 | 2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.496+49785_496+4980 others(20): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141262474 | |||||
| chr7:141262474
|
A | AATATATA others(11): Show |
1 | a0001c0002t0024g0002 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.496+49783_496+4980 others(22): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141262474 | |||||
| chr7:141262474
|
A | AATATATA others(13): Show |
3 | a0001c0001t0001g0012a0001c0001t0005g0014a0001c0002t0031g0063 | 3 | HG01106.hp2 HG02602.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.496+49781_496+4980 others(24): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141262474 | |||||
| chr7:141262474
|
A | AATATATA others(17): Show |
2 | a0001c0001t0020g0006a0001c0002t0040g0050 | 2 | HG02683.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.496+49777_496+4980 others(28): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141262474 | |||||
| chr7:141262474
|
AAT | A | 12 | a0001c0001t0006g0017a0001c0001t0011g0016a0001c0001t0012g0036others(9): Show | 12 | HG01106.hp1 HG01243.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.496+49799_496+4980 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141262474 | |||||
| chr7:141262474
|
AATAT | A | 20 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0004g0023others(17): Show | 20 | HG00544.hp1 HG01256.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.496+49797_496+4980 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141262474 | |||||
| chr7:141262474
|
AATATAT | A | 19 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0010g0021others(16): Show | 19 | HG01243.hp2 HG01255.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.496+49795_496+4980 others(10): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141262474 | |||||
| chr7:141262474
|
AATATATA others(1): Show |
A | 4 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+49793_496+4980 others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141262474 | |||||
| chr7:141262677
|
A | G | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.496+49973A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141262677 | ||||||
| chr7:141262800
|
G | T | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+50096G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141262800 | ||||||
| chr7:141263145
|
G | T | 7 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0035g0079others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+50441G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141263145 | ||||||
| chr7:141263183
|
G | C | 6 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0035g0079others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+50479G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141263183 | ||||||
| chr7:141263367
|
AG | A | 2 | a0001c0001t0015g0028a0001c0001t0025g0010 | 2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.496+50665delG | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141263367 | |||||
| chr7:141263375
|
G | A | 10 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(7): Show | 10 | HG01952.hp1 HG01978.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+50671G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141263375 | ||||||
| chr7:141263518
|
G | T | 1 | a0001c0001t0015g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.496+50814G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141263518 | ||||||
| chr7:141263769
|
G | A | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.496+51065G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141263769 | ||||||
| chr7:141264475
|
A | G | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+51771A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141264475 | ||||||
| chr7:141264637
|
AT | A | 6 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0035g0079others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+51936delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141264637 | |||||
| chr7:141265047
|
A | G | 8 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0002t0012g0045others(5): Show | 8 | HG00544.hp1 HG01106.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.496+52343A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141265047 | ||||||
| chr7:141265312
|
G | A | 6 | a0001c0001t0004g0029a0001c0001t0005g0008a0001c0001t0008g0004others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+52608G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141265312 | ||||||
| chr7:141265420
|
A | G | 2 | a0001c0001t0004g0024a0001c0002t0003g0052 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.496+52716A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141265420 | ||||||
| chr7:141265985
|
G | A | 5 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(2): Show | 5 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+53281G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141265985 | ||||||
| chr7:141266282
|
C | T | 1 | a0001c0002t0003g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.496+53578C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141266282 | ||||||
| chr7:141266623
|
A | G | 2 | a0001c0002t0007g0053a0001c0003t0019g0070 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.496+53919A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141266623 | ||||||
| chr7:141266663
|
G | A | 6 | a0001c0001t0004g0029a0001c0001t0005g0008a0001c0001t0008g0004others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+53959G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141266663 | ||||||
| chr7:141267016
|
G | A | 7 | a0001c0001t0022g0013a0001c0002t0001g0057a0001c0002t0007g0053others(4): Show | 7 | HG01243.hp2 HG01255.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+54312G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141267016 | ||||||
| chr7:141267169
|
G | A | 63 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(60): Show | 63 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.496+54465G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141267169 | ||||||
| chr7:141267172
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.496+54468C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141267172 | ||||||
| chr7:141267262
|
A | G | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+54558A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141267262 | ||||||
| chr7:141267380
|
A | G | 2 | a0001c0001t0003g0007a0001c0002t0030g0067 | 2 | HG02109.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.496+54676A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141267380 | ||||||
| chr7:141267495
|
T | C | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+54791T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141267495 | ||||||
| chr7:141267581
|
C | T | 9 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(6): Show | 9 | HG01952.hp1 HG01978.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.496+54877C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141267581 | ||||||
| chr7:141267817
|
T | A | 1 | a0001c0001t0004g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.496+55113T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141267817 | ||||||
| chr7:141267968
|
G | A | 5 | a0001c0001t0004g0029a0001c0001t0008g0004a0001c0001t0008g0030others(2): Show | 5 | HG02630.hp1 HG02647.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+55264G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141267968 | ||||||
| chr7:141268143
|
C | T | 1 | a0001c0003t0001g0074 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.496+55439C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141268143 | ||||||
| chr7:141268151
|
C | G | 2 | a0001c0002t0013g0059a0001c0002t0036g0069 | 2 | HG01255.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.496+55447C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141268151 | ||||||
| chr7:141268535
|
C | T | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+55831C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141268535 | ||||||
| chr7:141268614
|
T | C | 10 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(7): Show | 10 | HG01952.hp1 HG01978.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+55910T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141268614 | ||||||
| chr7:141269096
|
C | CT | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+56406dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141269096 | |||||
| chr7:141269175
|
A | C | 3 | a0001c0001t0034g0009a0001c0002t0009g0060a0001c0002t0015g0056 | 3 | HG03130.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.496+56471A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141269175 | ||||||
| chr7:141269711
|
C | T | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+57007C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141269711 | ||||||
| chr7:141269928
|
G | C | 1 | a0001c0003t0019g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.496+57224G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141269928 | ||||||
| chr7:141270152
|
A | G | 3 | a0001c0001t0034g0009a0001c0002t0009g0060a0001c0002t0015g0056 | 3 | HG03130.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.496+57448A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141270152 | ||||||
| chr7:141270582
|
C | A | 63 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(60): Show | 63 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.496+57878C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141270582 | ||||||
| chr7:141270785
|
C | G | 8 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0034g0009others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.496+58081C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141270785 | ||||||
| chr7:141270822
|
A | T | 1 | a0001c0001t0012g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.496+58118A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141270822 | ||||||
| chr7:141271078
|
A | G | 10 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(7): Show | 10 | HG01952.hp1 HG01978.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+58374A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141271078 | ||||||
| chr7:141271738
|
C | A | 10 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(7): Show | 10 | HG01952.hp1 HG01978.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+59034C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141271738 | ||||||
| chr7:141272072
|
C | A | 10 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(7): Show | 10 | HG01952.hp1 HG01978.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+59368C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141272072 | ||||||
| chr7:141272208
|
T | C | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+59504T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141272208 | ||||||
| chr7:141272621
|
A | G | 10 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(7): Show | 10 | HG01952.hp1 HG01978.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+59917A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141272621 | ||||||
| chr7:141272646
|
A | C | 1 | a0001c0001t0015g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.496+59942A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141272646 | ||||||
| chr7:141272677
|
C | T | 1 | a0001c0001t0004g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.496+59973C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141272677 | ||||||
| chr7:141272705
|
C | T | 2 | a0001c0001t0004g0024a0001c0002t0003g0052 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.496+60001C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141272705 | ||||||
| chr7:141272843
|
C | T | 34 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(31): Show | 34 | HG00544.hp2 HG01243.hp2 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.496+60139C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141272843 | ||||||
| chr7:141273166
|
T | TA | 7 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0035g0079others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+60469dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141273166 | |||||
| chr7:141273681
|
T | TA | 10 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(7): Show | 10 | HG01952.hp1 HG01978.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+60978dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141273681 | |||||
| chr7:141273701
|
C | T | 62 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(59): Show | 62 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(59): Show |
intron_variant | MODIFIER | c.496+60997C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141273701 | ||||||
| chr7:141273981
|
G | A | 25 | a0001c0001t0001g0012a0001c0001t0002g0027a0001c0001t0004g0024others(22): Show | 25 | HG01106.hp2 HG01891.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.496+61277G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141273981 | ||||||
| chr7:141274100
|
T | C | 17 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(14): Show | 17 | HG01891.hp1 HG01952.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.496+61396T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141274100 | ||||||
| chr7:141274154
|
C | T | 1 | a0001c0005t0001g0005 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.496+61450C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141274154 | ||||||
| chr7:141274210
|
G | T | 70 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0038others(67): Show | 70 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(67): Show |
intron_variant | MODIFIER | c.496+61506G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141274210 | ||||||
| chr7:141274459
|
A | G | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+61755A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141274459 | ||||||
| chr7:141274562
|
G | A | 1 | a0001c0001t0029g0026 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.496+61858G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141274562 | ||||||
| chr7:141274731
|
T | C | 12 | a0001c0001t0007g0011a0001c0001t0022g0013a0001c0002t0001g0057others(9): Show | 12 | HG00544.hp2 HG01243.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.496+62027T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141274731 | ||||||
| chr7:141274959
|
G | A | 2 | a0001c0001t0006g0025a0001c0002t0006g0040 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.496+62255G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141274959 | ||||||
| chr7:141275004
|
C | T | 1 | a0001c0003t0018g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.496+62300C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141275004 | ||||||
| chr7:141275088
|
T | G | 1 | a0001c0001t0007g0011 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.496+62384T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141275088 | ||||||
| chr7:141275200
|
C | T | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+62496C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141275200 | ||||||
| chr7:141275239
|
G | A | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.496+62535G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141275239 | ||||||
| chr7:141275307
|
A | G | 1 | a0001c0002t0031g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.496+62603A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141275307 | ||||||
| chr7:141275406
|
A | T | 6 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0035g0079others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+62702A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141275406 | ||||||
| chr7:141275446
|
G | A | 28 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+62742G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141275446 | ||||||
| chr7:141275617
|
A | G | 1 | a0001c0001t0020g0006 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.496+62913A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141275617 | ||||||
| chr7:141275897
|
C | T | 10 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(7): Show | 10 | HG01952.hp1 HG01978.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+63193C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141275897 | ||||||
| chr7:141275900
|
C | T | 6 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0035g0079others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+63196C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141275900 | ||||||
| chr7:141275901
|
G | A | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.496+63197G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141275901 | ||||||
| chr7:141275909
|
A | G | 7 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0035g0079others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+63205A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141275909 | ||||||
| chr7:141275991
|
T | G | 1 | a0001c0002t0008g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.496+63287T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141275991 | ||||||
| chr7:141276113
|
G | C | 2 | a0001c0002t0001g0042a0001c0002t0042g0054 | 2 | NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.496+63409G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141276113 | ||||||
| chr7:141276327
|
A | G | 1 | a0001c0001t0012g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.496+63623A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141276327 | ||||||
| chr7:141276574
|
C | A | 1 | a0001c0003t0001g0068 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.496+63870C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141276574 | ||||||
| chr7:141276592
|
GGGGTAGC others(12): Show |
G | 18 | a0001c0001t0001g0012a0001c0001t0002g0027a0001c0001t0004g0024others(15): Show | 18 | HG01106.hp2 HG01891.hp2 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.496+63889_496+6390 others(23): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141276592 | ||||||
| chr7:141276612
|
T | C | 18 | a0001c0001t0001g0012a0001c0001t0002g0027a0001c0001t0004g0024others(15): Show | 18 | HG01106.hp2 HG01891.hp2 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.496+63908T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141276612 | ||||||
| chr7:141276783
|
C | T | 2 | a0001c0001t0004g0024a0001c0002t0003g0052 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.496+64079C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141276783 | ||||||
| chr7:141277065
|
A | G | 73 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(70): Show | 73 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(70): Show |
intron_variant | MODIFIER | c.496+64361A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141277065 | ||||||
| chr7:141277182
|
G | T | 68 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(65): Show | 68 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(65): Show |
intron_variant | MODIFIER | c.496+64478G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141277182 | ||||||
| chr7:141277409
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.496+64705C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141277409 | ||||||
| chr7:141277606
|
T | C | 10 | a0001c0001t0001g0012a0001c0001t0002g0027a0001c0001t0005g0014others(7): Show | 10 | HG01106.hp2 HG02602.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.496+64902T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141277606 | ||||||
| chr7:141277671
|
C | T | 1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.496+64967C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141277671 | ||||||
| chr7:141278175
|
A | C | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.496+65471A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141278175 | ||||||
| chr7:141278309
|
C | T | 1 | a0001c0001t0003g0007 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.496+65605C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141278309 | ||||||
| chr7:141278342
|
G | A | 1 | a0001c0001t0014g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.496+65638G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141278342 | ||||||
| chr7:141278344
|
G | A | 1 | a0001c0001t0014g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.496+65640G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141278344 | ||||||
| chr7:141278377
|
T | C | 5 | a0001c0001t0007g0011a0001c0002t0013g0047a0001c0002t0013g0059others(2): Show | 5 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+65673T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141278377 | ||||||
| chr7:141278449
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.496+65745G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141278449 | ||||||
| chr7:141278549
|
C | CT | 73 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(70): Show | 73 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(70): Show |
intron_variant | MODIFIER | c.496+65845_496+6584 others(5): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141278549 | ||||||
| chr7:141278681
|
G | A | 5 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0015g0028others(2): Show | 5 | HG02486.hp1 HG02897.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+65977G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141278681 | ||||||
| chr7:141278942
|
C | T | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.496+66238C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141278942 | ||||||
| chr7:141279462
|
G | A | 2 | a0001c0001t0004g0024a0001c0002t0003g0052 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.496+66758G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141279462 | ||||||
| chr7:141279799
|
T | C | 11 | a0001c0001t0001g0015a0001c0001t0004g0023a0001c0001t0006g0017others(8): Show | 11 | HG01952.hp1 HG01952.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.496+67095T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141279799 | ||||||
| chr7:141279834
|
A | G | 19 | a0001c0001t0001g0012a0001c0001t0002g0027a0001c0001t0004g0024others(16): Show | 19 | HG01106.hp2 HG01891.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.496+67130A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141279834 | ||||||
| chr7:141279879
|
A | G | 1 | a0001c0001t0003g0020 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.496+67175A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141279879 | ||||||
| chr7:141280171
|
C | T | 8 | a0001c0001t0014g0039a0001c0001t0016g0037a0001c0001t0035g0079others(5): Show | 8 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+67467C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141280171 | ||||||
| chr7:141280681
|
G | C | 1 | a0001c0001t0015g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.496+67977G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141280681 | ||||||
| chr7:141280834
|
T | C | 66 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(63): Show | 66 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.496+68130T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141280834 | ||||||
| chr7:141280902
|
T | C | 1 | a0001c0001t0015g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.496+68198T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141280902 | ||||||
| chr7:141281312
|
A | AT | 15 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(12): Show | 15 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+68618dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141281312 | |||||
| chr7:141281411
|
T | C | 1 | a0001c0001t0007g0011 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.496+68707T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141281411 | ||||||
| chr7:141281482
|
T | C | 73 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(70): Show | 73 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(70): Show |
intron_variant | MODIFIER | c.496+68778T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141281482 | ||||||
| chr7:141281744
|
C | A | 4 | a0001c0002t0013g0047a0001c0002t0013g0059a0001c0002t0031g0063others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+69040C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141281744 | ||||||
| chr7:141281770
|
G | A | 1 | a0001c0002t0013g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.496+69066G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141281770 | ||||||
| chr7:141281837
|
C | A | 73 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(70): Show | 73 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(70): Show |
intron_variant | MODIFIER | c.496+69133C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141281837 | ||||||
| chr7:141282324
|
T | C | 1 | a0001c0001t0015g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.496+69620T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141282324 | ||||||
| chr7:141282537
|
G | A | 1 | a0001c0001t0009g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.496+69833G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141282537 | ||||||
| chr7:141282649
|
A | G | 15 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(12): Show | 15 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+69945A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141282649 | ||||||
| chr7:141282657
|
A | C | 1 | a0001c0001t0009g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.496+69953A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141282657 | ||||||
| chr7:141282710
|
C | T | 1 | a0001c0001t0004g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.496+70006C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141282710 | ||||||
| chr7:141282951
|
G | A | 8 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(5): Show | 8 | HG02109.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.496+70247G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141282951 | ||||||
| chr7:141283032
|
T | C | 1 | a0001c0002t0013g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.496+70328T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141283032 | ||||||
| chr7:141283259
|
C | G | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+70555C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141283259 | ||||||
| chr7:141283579
|
C | T | 1 | a0001c0001t0004g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.496+70875C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141283579 | ||||||
| chr7:141284199
|
C | T | 20 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0002g0019others(17): Show | 20 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.496+71495C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141284199 | ||||||
| chr7:141284575
|
C | T | 24 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0008g0030others(21): Show | 24 | HG00544.hp2 HG01243.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.496+71871C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141284575 | ||||||
| chr7:141284938
|
C | A | 2 | a0001c0001t0005g0008a0001c0001t0023g0018 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.496+72234C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141284938 | ||||||
| chr7:141284962
|
A | G | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.496+72258A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141284962 | ||||||
| chr7:141285056
|
T | TA | 15 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(12): Show | 15 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+72367dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141285056 | |||||
| chr7:141285080
|
G | T | 48 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(45): Show | 48 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.496+72376G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141285080 | ||||||
| chr7:141285083
|
A | C | 4 | a0001c0002t0013g0047a0001c0002t0013g0059a0001c0002t0031g0063others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+72379A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141285083 | ||||||
| chr7:141285125
|
C | A | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.496+72421C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141285125 | ||||||
| chr7:141285151
|
TTTC | T | 11 | a0001c0001t0001g0012a0001c0001t0004g0029a0001c0001t0006g0025others(8): Show | 11 | HG01106.hp2 HG01884.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.496+72450_496+7245 others(7): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141285151 | |||||
| chr7:141285152
|
TTC | T | 23 | a0001c0001t0001g0015a0001c0001t0003g0020a0001c0001t0005g0008others(20): Show | 23 | HG00544.hp2 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.496+72450_496+7245 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141285152 | |||||
| chr7:141285153
|
TC | T | 10 | a0001c0001t0001g0035a0001c0001t0006g0017a0001c0001t0009g0078others(7): Show | 10 | HG01978.hp2 HG02523.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.496+72450delC | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141285153 | ||||||
| chr7:141285154
|
C | T | 4 | a0001c0001t0002g0019a0001c0001t0023g0018a0001c0001t0025g0010others(1): Show | 4 | HG02486.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+72450C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141285154 | ||||||
| chr7:141285162
|
T | G | 1 | a0001c0001t0021g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.496+72458T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141285162 | ||||||
| chr7:141285177
|
T | C | 14 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(11): Show | 14 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.496+72473T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141285177 | ||||||
| chr7:141285268
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.496+72564A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141285268 | ||||||
| chr7:141285299
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.496+72595C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141285299 | ||||||
| chr7:141285396
|
G | C | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.496+72692G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141285396 | ||||||
| chr7:141285407
|
C | A | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+72703C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141285407 | ||||||
| chr7:141285409
|
C | T | 1 | a0001c0002t0001g0048 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.496+72705C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141285409 | ||||||
| chr7:141285644
|
C | T | 1 | a0001c0002t0006g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.496+72940C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141285644 | ||||||
| chr7:141285706
|
A | G | 2 | a0001c0002t0001g0048a0001c0002t0001g0065 | 2 | HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.496+73002A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141285706 | ||||||
| chr7:141285928
|
T | A | 48 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(45): Show | 48 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.496+73224T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141285928 | ||||||
| chr7:141286120
|
G | GA | 4 | a0001c0002t0013g0047a0001c0002t0013g0059a0001c0002t0031g0063others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+73425dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141286120 | |||||
| chr7:141286315
|
C | T | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+73611C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141286315 | ||||||
| chr7:141286519
|
G | A | 23 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0002g0019others(20): Show | 23 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.496+73815G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141286519 | ||||||
| chr7:141286754
|
G | A | 7 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+74050G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141286754 | ||||||
| chr7:141286937
|
A | G | 1 | a0001c0001t0009g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.496+74233A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141286937 | ||||||
| chr7:141287303
|
C | A | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.496+74599C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141287303 | ||||||
| chr7:141287387
|
G | A | 6 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(3): Show | 6 | HG02109.hp2 HG02486.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+74683G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141287387 | ||||||
| chr7:141287408
|
G | C | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.496+74704G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141287408 | ||||||
| chr7:141287451
|
G | T | 15 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(12): Show | 15 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+74747G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141287451 | ||||||
| chr7:141287976
|
G | A | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.496+75272G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141287976 | ||||||
| chr7:141288193
|
C | G | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.496+75489C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141288193 | ||||||
| chr7:141288195
|
CT | C | 26 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(23): Show | 26 | HG01243.hp2 HG01261.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.496+75502delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141288195 | |||||
| chr7:141288195
|
CTT | C | 15 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(12): Show | 15 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+75501_496+7550 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141288195 | |||||
| chr7:141288206
|
T | C | 27 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0008g0030others(24): Show | 27 | HG00544.hp2 HG01243.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.496+75502T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141288206 | ||||||
| chr7:141288236
|
GC | G | 6 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(3): Show | 6 | HG02109.hp2 HG02486.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+75533delC | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141288236 | ||||||
| chr7:141288454
|
AAGCAG | A | 6 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(3): Show | 6 | HG02109.hp2 HG02486.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+75755_496+7575 others(9): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141288454 | |||||
| chr7:141288465
|
C | T | 6 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(3): Show | 6 | HG02109.hp2 HG02486.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+75761C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141288465 | ||||||
| chr7:141288467
|
C | A | 6 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(3): Show | 6 | HG02109.hp2 HG02486.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+75763C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141288467 | ||||||
| chr7:141288469
|
G | T | 6 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(3): Show | 6 | HG02109.hp2 HG02486.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+75765G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141288469 | ||||||
| chr7:141288483
|
G | GA | 10 | a0001c0001t0001g0012a0001c0001t0004g0029a0001c0001t0014g0033others(7): Show | 10 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+75791dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141288483 | |||||
| chr7:141288811
|
G | A | 48 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(45): Show | 48 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.496+76107G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141288811 | ||||||
| chr7:141289072
|
G | A | 5 | a0001c0001t0003g0020a0001c0001t0006g0025a0001c0001t0010g0021others(2): Show | 5 | HG02630.hp2 HG03139.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+76368G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141289072 | ||||||
| chr7:141289466
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.496+76762A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141289466 | ||||||
| chr7:141289489
|
G | A | 15 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(12): Show | 15 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+76785G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141289489 | ||||||
| chr7:141289714
|
C | CA | 9 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0008g0030others(6): Show | 9 | HG01978.hp1 HG02258.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.496+77027dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141289714 | |||||
| chr7:141289714
|
C | CAA | 17 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0003g0007others(14): Show | 17 | HG00544.hp1 HG01106.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.496+77026_496+7702 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141289714 | |||||
| chr7:141289714
|
C | CAAA | 4 | a0001c0001t0002g0027a0001c0001t0004g0024a0001c0001t0038g0034others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+77025_496+7702 others(7): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141289714 | |||||
| chr7:141290052
|
A | T | 15 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(12): Show | 15 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+77348A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141290052 | ||||||
| chr7:141290239
|
A | G | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+77535A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141290239 | ||||||
| chr7:141290283
|
G | T | 15 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(12): Show | 15 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+77579G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141290283 | ||||||
| chr7:141290519
|
TCACACAC others(13): Show |
T | 6 | a0001c0001t0022g0013a0001c0002t0001g0057a0001c0002t0001g0064others(3): Show | 6 | HG01243.hp2 HG01261.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+77829_496+7784 others(24): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141290519 | |||||
| chr7:141290611
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016others(3): Show | 6 | HG01952.hp1 HG01978.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+77907G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141290611 | ||||||
| chr7:141290724
|
A | G | 15 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(12): Show | 15 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+78020A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141290724 | ||||||
| chr7:141290927
|
G | T | 24 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0008g0030others(21): Show | 24 | HG00544.hp2 HG01243.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.496+78223G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141290927 | ||||||
| chr7:141291048
|
T | C | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.496+78344T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141291048 | ||||||
| chr7:141291195
|
C | T | 1 | a0001c0003t0001g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.496+78491C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141291195 | ||||||
| chr7:141291343
|
A | G | 17 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(14): Show | 17 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.496+78639A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141291343 | ||||||
| chr7:141291370
|
A | G | 1 | a0001c0001t0009g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.496+78666A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141291370 | ||||||
| chr7:141291636
|
C | A | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+78932C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141291636 | ||||||
| chr7:141291637
|
C | A | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+78933C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141291637 | ||||||
| chr7:141291671
|
G | A | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+78967G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141291671 | ||||||
| chr7:141291718
|
G | T | 18 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(15): Show | 18 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.496+79014G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141291718 | ||||||
| chr7:141291741
|
G | A | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.496+79037G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141291741 | ||||||
| chr7:141291902
|
G | A | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+79198G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141291902 | ||||||
| chr7:141291926
|
AT | A | 40 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0080others(37): Show | 40 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.496+79239delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141291926 | |||||
| chr7:141291926
|
ATT | A | 28 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(25): Show | 28 | HG00544.hp2 HG01243.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.496+79238_496+7923 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141291926 | |||||
| chr7:141291926
|
ATTT | A | 4 | a0001c0001t0009g0078a0001c0001t0044g0001a0001c0002t0026g0041others(1): Show | 4 | HG01256.hp1 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+79237_496+7923 others(7): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141291926 | |||||
| chr7:141291943
|
T | C | 2 | a0001c0001t0005g0008a0001c0001t0023g0018 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.496+79239T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141291943 | ||||||
| chr7:141291979
|
C | G | 1 | a0001c0001t0015g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.496+79275C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141291979 | ||||||
| chr7:141292424
|
G | C | 16 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(13): Show | 16 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.496+79720G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141292424 | ||||||
| chr7:141292563
|
A | G | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+79859A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141292563 | ||||||
| chr7:141292634
|
C | CT | 15 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0015g0028others(12): Show | 15 | HG00544.hp2 HG02027.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+79951dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141292634 | |||||
| chr7:141292634
|
C | CTT | 24 | a0001c0001t0001g0015a0001c0001t0005g0008a0001c0001t0006g0017others(21): Show | 24 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.496+79950_496+7995 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141292634 | |||||
| chr7:141292634
|
CT | C | 15 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(12): Show | 15 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+79951delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141292634 | |||||
| chr7:141292660
|
T | C | 17 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(14): Show | 17 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.496+79956T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141292660 | ||||||
| chr7:141292820
|
T | G | 29 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(26): Show | 29 | HG00544.hp2 HG01243.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+80116T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141292820 | ||||||
| chr7:141292933
|
C | A | 1 | a0001c0001t0015g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.496+80229C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141292933 | ||||||
| chr7:141292933
|
C | T | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+80229C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141292933 | ||||||
| chr7:141292956
|
A | C | 25 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0002g0027others(22): Show | 25 | HG00544.hp1 HG01106.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.496+80252A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141292956 | ||||||
| chr7:141293147
|
T | G | 6 | a0001c0001t0009g0078a0001c0001t0044g0001a0001c0002t0013g0047others(3): Show | 6 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+80443T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141293147 | ||||||
| chr7:141293193
|
A | G | 7 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(4): Show | 7 | HG02109.hp1 HG02486.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+80489A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141293193 | ||||||
| chr7:141293217
|
C | T | 48 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(45): Show | 48 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.496+80513C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141293217 | ||||||
| chr7:141293230
|
G | T | 25 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0002g0027others(22): Show | 25 | HG00544.hp1 HG01106.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.496+80526G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141293230 | ||||||
| chr7:141293273
|
G | A | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+80569G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141293273 | ||||||
| chr7:141293570
|
A | C | 1 | a0001c0001t0009g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.496+80866A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141293570 | ||||||
| chr7:141293615
|
ATG | A | 3 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016 | 3 | HG02258.hp2 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.496+80913_496+8091 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141293615 | |||||
| chr7:141293838
|
G | A | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+81134G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141293838 | ||||||
| chr7:141293892
|
G | T | 16 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(13): Show | 16 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.496+81188G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141293892 | ||||||
| chr7:141294090
|
G | A | 1 | a0001c0002t0008g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.496+81386G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141294090 | ||||||
| chr7:141294090
|
G | C | 28 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0002g0019others(25): Show | 28 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.496+81386G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141294090 | ||||||
| chr7:141294287
|
C | T | 1 | a0001c0001t0015g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.496+81583C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141294287 | ||||||
| chr7:141294292
|
C | T | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.496+81588C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141294292 | ||||||
| chr7:141294482
|
A | C | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+81778A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141294482 | ||||||
| chr7:141294506
|
T | G | 4 | a0001c0002t0013g0047a0001c0002t0013g0059a0001c0002t0031g0063others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+81802T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141294506 | ||||||
| chr7:141294523
|
T | A | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.496+81819T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141294523 | ||||||
| chr7:141294816
|
T | C | 1 | a0001c0001t0003g0007 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.496+82112T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141294816 | ||||||
| chr7:141294923
|
C | T | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.496+82219C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141294923 | ||||||
| chr7:141295734
|
CGGG | C | 29 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(26): Show | 29 | HG00544.hp2 HG01243.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+83033_496+8303 others(7): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141295734 | |||||
| chr7:141295780
|
C | A | 18 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(15): Show | 18 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.496+83076C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141295780 | ||||||
| chr7:141296074
|
C | CT | 6 | a0001c0002t0013g0047a0001c0002t0013g0059a0001c0002t0031g0063others(3): Show | 6 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+83383dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141296074 | |||||
| chr7:141296124
|
A | G | 29 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(26): Show | 29 | HG00544.hp2 HG01243.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+83420A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141296124 | ||||||
| chr7:141296218
|
C | A | 29 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(26): Show | 29 | HG00544.hp2 HG01243.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+83514C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141296218 | ||||||
| chr7:141296219
|
C | T | 29 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(26): Show | 29 | HG00544.hp2 HG01243.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+83515C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141296219 | ||||||
| chr7:141296290
|
A | G | 4 | a0001c0002t0013g0047a0001c0002t0013g0059a0001c0002t0031g0063others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+83586A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141296290 | ||||||
| chr7:141296320
|
A | G | 73 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(70): Show | 73 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(70): Show |
intron_variant | MODIFIER | c.496+83616A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141296320 | ||||||
| chr7:141296329
|
A | G | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.496+83625A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141296329 | ||||||
| chr7:141296363
|
C | T | 1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.496+83659C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141296363 | ||||||
| chr7:141296572
|
A | T | 5 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(2): Show | 5 | HG02486.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+83868A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141296572 | ||||||
| chr7:141296607
|
G | C | 73 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(70): Show | 73 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(70): Show |
intron_variant | MODIFIER | c.496+83903G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141296607 | ||||||
| chr7:141296617
|
A | T | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+83913A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141296617 | ||||||
| chr7:141296649
|
T | A | 25 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0002g0027others(22): Show | 25 | HG00544.hp1 HG01106.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.496+83945T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141296649 | ||||||
| chr7:141296838
|
A | G | 29 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(26): Show | 29 | HG00544.hp2 HG01243.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+84134A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141296838 | ||||||
| chr7:141297113
|
G | A | 25 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0002g0027others(22): Show | 25 | HG00544.hp1 HG01106.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.496+84409G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141297113 | ||||||
| chr7:141297394
|
G | A | 29 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(26): Show | 29 | HG00544.hp2 HG01243.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+84690G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141297394 | ||||||
| chr7:141297531
|
A | G | 1 | a0001c0001t0015g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.496+84827A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141297531 | ||||||
| chr7:141297575
|
C | G | 29 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(26): Show | 29 | HG00544.hp2 HG01243.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+84871C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141297575 | ||||||
| chr7:141297597
|
A | G | 16 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(13): Show | 16 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.496+84893A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141297597 | ||||||
| chr7:141297798
|
A | G | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.496+85094A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141297798 | ||||||
| chr7:141298272
|
G | A | 9 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0002t0007g0073others(6): Show | 9 | HG00544.hp1 HG01106.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.496+85568G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141298272 | ||||||
| chr7:141298290
|
T | C | 1 | a0001c0002t0005g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.496+85586T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141298290 | ||||||
| chr7:141298922
|
C | A | 1 | a0001c0002t0003g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.496+86218C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141298922 | ||||||
| chr7:141299030
|
G | T | 4 | a0001c0002t0013g0047a0001c0002t0013g0059a0001c0002t0031g0063others(1): Show | 4 | HG00544.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+86326G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141299030 | ||||||
| chr7:141299696
|
C | T | 2 | a0001c0002t0032g0071a0001c0005t0001g0005 | 2 | HG01255.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.496+86992C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141299696 | ||||||
| chr7:141299727
|
T | C | 1 | a0001c0003t0001g0068 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.496+87023T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141299727 | ||||||
| chr7:141299984
|
A | G | 3 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0001t0025g0010 | 3 | HG02486.hp1 HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.496+87280A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141299984 | ||||||
| chr7:141300085
|
C | A | 1 | a0001c0002t0031g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.496+87381C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141300085 | ||||||
| chr7:141300213
|
T | C | 16 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(13): Show | 16 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.496+87509T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141300213 | ||||||
| chr7:141300368
|
A | G | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+87664A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141300368 | ||||||
| chr7:141301247
|
G | A | 26 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0002g0027others(23): Show | 26 | HG00544.hp1 HG01106.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.496+88543G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141301247 | ||||||
| chr7:141301611
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.496+88907G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141301611 | ||||||
| chr7:141301826
|
C | T | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.496+89122C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141301826 | ||||||
| chr7:141301870
|
C | T | 2 | a0001c0001t0005g0014a0001c0002t0024g0002 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.496+89166C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141301870 | ||||||
| chr7:141302327
|
A | G | 15 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(12): Show | 15 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+89623A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141302327 | ||||||
| chr7:141302436
|
T | C | 31 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(28): Show | 31 | HG00544.hp1 HG01106.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.496+89732T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141302436 | ||||||
| chr7:141302664
|
A | G | 16 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(13): Show | 16 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.496+89960A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141302664 | ||||||
| chr7:141302723
|
T | C | 1 | a0001c0001t0003g0007 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.496+90019T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141302723 | ||||||
| chr7:141303004
|
A | C | 2 | a0001c0001t0004g0023a0001c0002t0042g0054 | 2 | HG01952.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.496+90300A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141303004 | ||||||
| chr7:141303245
|
T | C | 30 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(27): Show | 30 | HG00544.hp1 HG01106.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.496+90541T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141303245 | ||||||
| chr7:141303362
|
A | G | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+90658A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141303362 | ||||||
| chr7:141303437
|
G | A | 18 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0008g0030others(15): Show | 18 | HG01243.hp2 HG01261.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.496+90733G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141303437 | ||||||
| chr7:141303443
|
G | T | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.496+90739G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141303443 | ||||||
| chr7:141303632
|
G | A | 15 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0004g0029others(12): Show | 15 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+90928G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141303632 | ||||||
| chr7:141303657
|
G | T | 2 | a0001c0001t0005g0008a0001c0001t0023g0018 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.496+90953G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141303657 | ||||||
| chr7:141303911
|
T | C | 18 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0008g0030others(15): Show | 18 | HG01243.hp2 HG01261.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.496+91207T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141303911 | ||||||
| chr7:141303915
|
G | A | 1 | a0001c0001t0007g0011 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.496+91211G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141303915 | ||||||
| chr7:141304222
|
C | G | 51 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(48): Show | 51 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.496+91518C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141304222 | ||||||
| chr7:141304510
|
G | T | 7 | a0001c0001t0014g0033a0001c0001t0016g0037a0001c0001t0028g0022others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+91806G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141304510 | ||||||
| chr7:141304514
|
C | G | 1 | a0001c0003t0001g0068 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.496+91810C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141304514 | ||||||
| chr7:141304618
|
GGCTTCAG others(7): Show |
G | 1 | a0001c0001t0004g0023 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.496+91917_496+9193 others(18): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141304618 | |||||
| chr7:141304867
|
G | A | 4 | a0001c0001t0003g0007a0001c0001t0016g0037a0001c0002t0002g0043others(1): Show | 4 | HG01891.hp1 HG02897.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+92163G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141304867 | ||||||
| chr7:141305121
|
A | G | 1 | a0001c0002t0042g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.496+92417A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141305121 | ||||||
| chr7:141305171
|
C | A | 8 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0006g0025others(5): Show | 8 | HG02486.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+92467C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141305171 | ||||||
| chr7:141305813
|
A | G | 8 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0006g0025others(5): Show | 8 | HG02486.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+93109A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141305813 | ||||||
| chr7:141306204
|
A | C | 63 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(60): Show | 63 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.496+93500A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141306204 | ||||||
| chr7:141306205
|
A | G | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.496+93501A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141306205 | ||||||
| chr7:141306364
|
C | T | 8 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0006g0025others(5): Show | 8 | HG02486.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+93660C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141306364 | ||||||
| chr7:141306461
|
C | G | 21 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0020others(18): Show | 21 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.496+93757C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141306461 | ||||||
| chr7:141306621
|
GT | G | 10 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0003g0007others(7): Show | 10 | HG01255.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.496+93931delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141306621 | |||||
| chr7:141306716
|
G | C | 1 | a0001c0001t0003g0007 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.496+94012G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141306716 | ||||||
| chr7:141306800
|
C | T | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.496+94096C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141306800 | ||||||
| chr7:141307113
|
C | T | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.496+94409C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141307113 | ||||||
| chr7:141307178
|
A | G | 21 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0020others(18): Show | 21 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.496+94474A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141307178 | ||||||
| chr7:141307179
|
C | CT | 72 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(69): Show | 72 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.496+94481dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141307179 | |||||
| chr7:141307210
|
A | G | 72 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(69): Show | 72 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.496+94506A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141307210 | ||||||
| chr7:141307289
|
G | T | 8 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0006g0025others(5): Show | 8 | HG02486.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+94585G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141307289 | ||||||
| chr7:141307315
|
C | G | 4 | a0001c0001t0002g0027a0001c0001t0015g0028a0001c0002t0001g0042others(1): Show | 4 | HG02615.hp1 HG03516.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+94611C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141307315 | ||||||
| chr7:141307341
|
C | T | 1 | a0001c0001t0035g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.496+94637C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141307341 | ||||||
| chr7:141307545
|
A | G | 8 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0006g0025others(5): Show | 8 | HG02486.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+94841A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141307545 | ||||||
| chr7:141307917
|
A | G | 47 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(44): Show | 47 | HG01106.hp2 HG01243.hp1 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.496+95213A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141307917 | ||||||
| chr7:141308238
|
G | A | 4 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(1): Show | 4 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+95534G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141308238 | ||||||
| chr7:141308415
|
T | A | 1 | a0001c0001t0001g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.496+95711T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141308415 | ||||||
| chr7:141308577
|
C | A | 34 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(31): Show | 34 | HG01106.hp2 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.496+95873C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141308577 | ||||||
| chr7:141308678
|
T | C | 1 | a0001c0002t0032g0071 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.496+95974T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141308678 | ||||||
| chr7:141309148
|
G | GA | 5 | a0001c0001t0004g0023a0001c0001t0016g0037a0001c0002t0002g0043others(2): Show | 5 | HG01891.hp1 HG01952.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+96450dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141309148 | |||||
| chr7:141309594
|
G | T | 7 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0006g0025others(4): Show | 7 | HG02572.hp1 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+96890G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141309594 | ||||||
| chr7:141309998
|
G | A | 2 | a0001c0001t0034g0009a0001c0002t0009g0060 | 2 | HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.496+97294G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141309998 | ||||||
| chr7:141310131
|
T | G | 2 | a0001c0001t0006g0025a0001c0002t0006g0040 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.496+97427T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141310131 | ||||||
| chr7:141310314
|
A | G | 72 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(69): Show | 72 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.496+97610A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141310314 | ||||||
| chr7:141310369
|
C | T | 39 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0020others(36): Show | 39 | HG01106.hp2 HG01243.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.496+97665C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141310369 | ||||||
| chr7:141310622
|
G | A | 35 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0020others(32): Show | 35 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.496+97918G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141310622 | ||||||
| chr7:141310692
|
A | G | 35 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0020others(32): Show | 35 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.496+97988A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141310692 | ||||||
| chr7:141310960
|
A | C | 35 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0020others(32): Show | 35 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.496+98256A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141310960 | ||||||
| chr7:141311254
|
C | T | 72 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(69): Show | 72 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.496+98550C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141311254 | ||||||
| chr7:141311449
|
A | G | 1 | a0001c0002t0002g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.496+98745A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141311449 | ||||||
| chr7:141312140
|
T | C | 72 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(69): Show | 72 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.496+99436T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141312140 | ||||||
| chr7:141312215
|
A | C | 76 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(73): Show | 76 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(73): Show |
intron_variant | MODIFIER | c.496+99511A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141312215 | ||||||
| chr7:141312236
|
G | A | 4 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(1): Show | 4 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+99532G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141312236 | ||||||
| chr7:141312513
|
T | C | 41 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(38): Show | 41 | HG00544.hp1 HG01106.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.496+99809T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141312513 | ||||||
| chr7:141312625
|
A | G | 1 | a0001c0002t0007g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.496+99921A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141312625 | ||||||
| chr7:141312655
|
A | G | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.496+99951A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141312655 | ||||||
| chr7:141312816
|
A | G | 72 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(69): Show | 72 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.496+100112A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141312816 | ||||||
| chr7:141312927
|
A | T | 49 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(46): Show | 49 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.496+100223A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141312927 | ||||||
| chr7:141312958
|
G | A | 1 | a0001c0002t0001g0048 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.496+100254G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141312958 | ||||||
| chr7:141313000
|
G | C | 1 | a0001c0002t0011g0044 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.496+100296G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141313000 | ||||||
| chr7:141313123
|
A | G | 28 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(25): Show | 28 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.496+100419A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141313123 | ||||||
| chr7:141313205
|
G | T | 4 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(1): Show | 4 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+100501G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141313205 | ||||||
| chr7:141313778
|
T | TAAAAAAA others(316): Show |
1 | a0001c0002t0001g0057 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.496+101086_496+101 others(329): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141313778 | |||||
| chr7:141313778
|
T | TAAAAAAA others(317): Show |
2 | a0001c0002t0007g0053a0001c0003t0001g0068 | 2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.496+101086_496+101 others(330): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141313778 | |||||
| chr7:141313778
|
T | TAAAAAAA others(320): Show |
1 | a0001c0002t0001g0064 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.496+101086_496+101 others(333): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141313778 | |||||
| chr7:141313943
|
G | A | 2 | a0001c0001t0008g0004a0001c0001t0009g0078 | 2 | HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.496+101239G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141313943 | ||||||
| chr7:141314457
|
G | A | 5 | a0001c0001t0014g0033a0001c0001t0014g0039a0001c0001t0028g0022others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+101753G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141314457 | ||||||
| chr7:141314466
|
C | G | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.496+101762C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141314466 | ||||||
| chr7:141314555
|
C | A | 1 | a0001c0002t0041g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.496+101851C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141314555 | ||||||
| chr7:141314598
|
C | G | 3 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016 | 3 | HG02258.hp2 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.496+101894C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141314598 | ||||||
| chr7:141314600
|
C | T | 45 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(42): Show | 45 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.496+101896C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141314600 | ||||||
| chr7:141314622
|
G | A | 1 | a0001c0001t0003g0007 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.496+101918G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141314622 | ||||||
| chr7:141314723
|
T | A | 1 | a0001c0002t0012g0045 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.496+102019T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141314723 | ||||||
| chr7:141315057
|
A | G | 1 | a0001c0003t0019g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.496+102353A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141315057 | ||||||
| chr7:141315474
|
TCACTTTC others(6): Show |
T | 5 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(2): Show | 5 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+102771_496+102 others(19): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141315474 | ||||||
| chr7:141315491
|
T | A | 5 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(2): Show | 5 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+102787T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141315491 | ||||||
| chr7:141315492
|
T | A | 5 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(2): Show | 5 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+102788T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141315492 | ||||||
| chr7:141315495
|
CAAA | C | 5 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(2): Show | 5 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+102792_496+102 others(9): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141315495 | ||||||
| chr7:141315785
|
G | A | 1 | a0001c0002t0003g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.496+103081G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141315785 | ||||||
| chr7:141315850
|
G | C | 44 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(41): Show | 44 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.496+103146G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141315850 | ||||||
| chr7:141316062
|
G | A | 44 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(41): Show | 44 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.496+103358G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141316062 | ||||||
| chr7:141316552
|
C | CTGTG | 6 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(3): Show | 6 | HG01243.hp2 HG01978.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+103862_496+103 others(10): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141316552 | |||||
| chr7:141316595
|
G | A | 7 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(4): Show | 7 | HG01243.hp2 HG01978.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+103891G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141316595 | ||||||
| chr7:141316663
|
G | T | 7 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(4): Show | 7 | HG01243.hp2 HG01978.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+103959G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141316663 | ||||||
| chr7:141316729
|
T | C | 2 | a0001c0001t0004g0029a0001c0001t0033g0031 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.496+104025T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141316729 | ||||||
| chr7:141316763
|
A | T | 7 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(4): Show | 7 | HG01243.hp2 HG01978.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+104059A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141316763 | ||||||
| chr7:141316850
|
T | C | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+104146T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141316850 | ||||||
| chr7:141316866
|
A | G | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.496+104162A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141316866 | ||||||
| chr7:141317067
|
CT | C | 6 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(3): Show | 6 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+104371delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141317067 | |||||
| chr7:141317255
|
G | A | 7 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(4): Show | 7 | HG01243.hp2 HG01978.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+104551G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141317255 | ||||||
| chr7:141317361
|
T | G | 7 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(4): Show | 7 | HG01243.hp2 HG01978.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+104657T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141317361 | ||||||
| chr7:141317513
|
G | A | 7 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(4): Show | 7 | HG01243.hp2 HG01978.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+104809G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141317513 | ||||||
| chr7:141317560
|
C | T | 7 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(4): Show | 7 | HG01243.hp2 HG01978.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+104856C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141317560 | ||||||
| chr7:141317634
|
A | G | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.496+104930A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141317634 | ||||||
| chr7:141317843
|
G | T | 44 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(41): Show | 44 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.496+105139G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141317843 | ||||||
| chr7:141318302
|
A | G | 2 | a0001c0001t0006g0025a0001c0002t0006g0040 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.496+105598A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141318302 | ||||||
| chr7:141318439
|
G | A | 51 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(48): Show | 51 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.496+105735G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141318439 | ||||||
| chr7:141318529
|
C | A | 2 | a0001c0001t0006g0025a0001c0002t0006g0040 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.496+105825C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141318529 | ||||||
| chr7:141318619
|
T | C | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.496+105915T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141318619 | ||||||
| chr7:141318708
|
G | T | 4 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(1): Show | 4 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+106004G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141318708 | ||||||
| chr7:141319026
|
TG | T | 2 | a0001c0001t0008g0030a0001c0004t0043g0032 | 2 | HG02109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.496+106323delG | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141319026 | ||||||
| chr7:141319315
|
T | C | 43 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(40): Show | 43 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.496+106611T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141319315 | ||||||
| chr7:141319418
|
T | C | 4 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(1): Show | 4 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+106714T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141319418 | ||||||
| chr7:141319484
|
T | C | 45 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(42): Show | 45 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.496+106780T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141319484 | ||||||
| chr7:141319502
|
G | A | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.496+106798G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141319502 | ||||||
| chr7:141319585
|
C | T | 45 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(42): Show | 45 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.496+106881C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141319585 | ||||||
| chr7:141319589
|
A | G | 4 | a0001c0002t0013g0047a0001c0002t0031g0063a0001c0002t0032g0071others(1): Show | 4 | HG00544.hp2 HG01255.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+106885A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141319589 | ||||||
| chr7:141319712
|
G | A | 45 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(42): Show | 45 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.496+107008G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141319712 | ||||||
| chr7:141319772
|
G | A | 2 | a0001c0002t0016g0072a0002c0006t0039g0061 | 2 | HG01261.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.496+107068G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141319772 | ||||||
| chr7:141319801
|
C | A | 45 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(42): Show | 45 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.496+107097C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141319801 | ||||||
| chr7:141319924
|
G | A | 4 | a0001c0002t0013g0047a0001c0002t0031g0063a0001c0002t0032g0071others(1): Show | 4 | HG00544.hp2 HG01255.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+107220G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141319924 | ||||||
| chr7:141320056
|
T | A | 44 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(41): Show | 44 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.496+107352T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141320056 | ||||||
| chr7:141320423
|
C | T | 42 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(39): Show | 42 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.496+107719C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141320423 | ||||||
| chr7:141320514
|
A | G | 1 | a0001c0002t0007g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.496+107810A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141320514 | ||||||
| chr7:141320947
|
T | G | 56 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(53): Show | 56 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.496+108243T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141320947 | ||||||
| chr7:141320987
|
C | T | 45 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(42): Show | 45 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.496+108283C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141320987 | ||||||
| chr7:141321044
|
C | T | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+108340C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141321044 | ||||||
| chr7:141321052
|
A | G | 43 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(40): Show | 43 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.496+108348A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141321052 | ||||||
| chr7:141321107
|
C | T | 43 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(40): Show | 43 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.496+108403C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141321107 | ||||||
| chr7:141321153
|
T | C | 1 | a0001c0001t0020g0006 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.496+108449T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141321153 | ||||||
| chr7:141321344
|
G | A | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+108640G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141321344 | ||||||
| chr7:141321383
|
T | C | 45 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(42): Show | 45 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.496+108679T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141321383 | ||||||
| chr7:141321465
|
A | C | 45 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(42): Show | 45 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.496+108761A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141321465 | ||||||
| chr7:141321825
|
T | TC | 42 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0020others(39): Show | 42 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.496+109121_496+109 others(7): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141321825 | ||||||
| chr7:141321825
|
T | TCA | 2 | a0001c0001t0006g0025a0001c0002t0006g0040 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.496+109121_496+109 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141321825 | ||||||
| chr7:141321826
|
T | A | 44 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0020others(41): Show | 44 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.496+109122T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141321826 | ||||||
| chr7:141321826
|
T | C | 1 | a0001c0001t0003g0007 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.496+109122T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141321826 | ||||||
| chr7:141321894
|
A | G | 45 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(42): Show | 45 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.496+109190A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141321894 | ||||||
| chr7:141321993
|
G | A | 45 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(42): Show | 45 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.496+109289G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141321993 | ||||||
| chr7:141321994
|
T | TTC | 45 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(42): Show | 45 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.496+109292_496+109 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141321994 | |||||
| chr7:141322150
|
T | A | 45 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(42): Show | 45 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.496+109446T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141322150 | ||||||
| chr7:141322192
|
G | A | 45 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(42): Show | 45 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.496+109488G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141322192 | ||||||
| chr7:141322230
|
T | C | 2 | a0001c0001t0006g0025a0001c0002t0006g0040 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.496+109526T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141322230 | ||||||
| chr7:141322237
|
A | G | 45 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(42): Show | 45 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.496+109533A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141322237 | ||||||
| chr7:141322253
|
C | T | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.496+109549C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141322253 | ||||||
| chr7:141322302
|
G | A | 4 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(1): Show | 4 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+109598G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141322302 | ||||||
| chr7:141322363
|
TA | T | 34 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(31): Show | 34 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.496+109677delA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141322363 | |||||
| chr7:141322363
|
TAA | T | 22 | a0001c0001t0001g0012a0001c0001t0004g0023a0001c0001t0005g0008others(19): Show | 22 | HG00544.hp2 HG01106.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.496+109676_496+109 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141322363 | |||||
| chr7:141322389
|
G | C | 1 | a0001c0002t0007g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.496+109685G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141322389 | ||||||
| chr7:141322425
|
C | T | 24 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(21): Show | 24 | HG00544.hp2 HG01255.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.496+109721C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141322425 | ||||||
| chr7:141322572
|
A | G | 1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.496+109868A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141322572 | ||||||
| chr7:141322576
|
A | G | 2 | a0001c0001t0006g0025a0001c0002t0006g0040 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.496+109872A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141322576 | ||||||
| chr7:141322584
|
A | G | 24 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(21): Show | 24 | HG00544.hp2 HG01255.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.496+109880A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141322584 | ||||||
| chr7:141322793
|
A | G | 24 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(21): Show | 24 | HG00544.hp2 HG01255.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.496+110089A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141322793 | ||||||
| chr7:141322853
|
C | A | 21 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0008g0030others(18): Show | 21 | HG00544.hp2 HG01255.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.496+110149C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141322853 | ||||||
| chr7:141322914
|
C | T | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+110210C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141322914 | ||||||
| chr7:141322995
|
C | G | 3 | a0001c0002t0011g0044a0001c0002t0037g0075a0001c0003t0019g0070 | 3 | HG01884.hp1 HG02027.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.496+110291C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141322995 | ||||||
| chr7:141323072
|
T | G | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+110368T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141323072 | ||||||
| chr7:141323084
|
G | A | 2 | a0001c0001t0005g0008a0001c0001t0023g0018 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.496+110380G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141323084 | ||||||
| chr7:141323101
|
C | T | 24 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(21): Show | 24 | HG00544.hp2 HG01255.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.496+110397C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141323101 | ||||||
| chr7:141323325
|
G | A | 22 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(19): Show | 22 | HG00544.hp2 HG01255.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.496+110621G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141323325 | ||||||
| chr7:141323399
|
G | T | 1 | a0001c0001t0004g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.496+110695G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141323399 | ||||||
| chr7:141323519
|
G | A | 22 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(19): Show | 22 | HG00544.hp2 HG01255.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.496+110815G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141323519 | ||||||
| chr7:141323771
|
A | G | 4 | a0001c0002t0013g0047a0001c0002t0031g0063a0001c0002t0032g0071others(1): Show | 4 | HG00544.hp2 HG01255.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+111067A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141323771 | ||||||
| chr7:141324006
|
T | G | 29 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(26): Show | 29 | HG00544.hp2 HG01243.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.496+111302T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141324006 | ||||||
| chr7:141324416
|
G | GT | 8 | a0001c0001t0001g0080a0001c0001t0025g0010a0001c0002t0001g0065others(5): Show | 8 | HG00544.hp1 HG01106.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+111749dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141324416 | |||||
| chr7:141324416
|
G | GTT | 6 | a0001c0001t0001g0038a0001c0001t0004g0024a0001c0001t0007g0011others(3): Show | 6 | HG01261.hp1 HG02683.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+111748_496+111 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141324416 | |||||
| chr7:141324416
|
GT | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0012g0036others(5): Show | 8 | HG01106.hp2 HG02258.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+111749delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141324416 | |||||
| chr7:141324416
|
GTT | G | 7 | a0001c0001t0003g0007a0001c0001t0003g0020a0001c0001t0004g0029others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+111748_496+111 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141324416 | |||||
| chr7:141324416
|
GTTTTTTT others(4): Show |
G | 4 | a0001c0002t0013g0047a0001c0002t0031g0063a0001c0002t0032g0071others(1): Show | 4 | HG00544.hp2 HG01255.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+111739_496+111 others(17): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141324416 | |||||
| chr7:141324416
|
GTTTTTTT others(5): Show |
G | 19 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(16): Show | 19 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.496+111738_496+111 others(18): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141324416 | |||||
| chr7:141324416
|
GTTTTTTT others(6): Show |
G | 4 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(1): Show | 4 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+111737_496+111 others(19): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141324416 | |||||
| chr7:141324416
|
GTTTTTTT others(11): Show |
G | 1 | a0001c0001t0035g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.496+111732_496+111 others(24): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141324416 | |||||
| chr7:141324416
|
GTTTTTTT others(16): Show |
G | 1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.496+111727_496+111 others(29): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141324416 | |||||
| chr7:141324418
|
T | TG | 2 | a0001c0001t0015g0028a0001c0002t0008g0003 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.496+111714_496+111 others(7): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141324418 | ||||||
| chr7:141324419
|
T | G | 2 | a0001c0002t0001g0042a0001c0002t0005g0049 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.496+111715T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141324419 | ||||||
| chr7:141324436
|
T | G | 4 | a0001c0002t0013g0047a0001c0002t0031g0063a0001c0002t0032g0071others(1): Show | 4 | HG00544.hp2 HG01255.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+111732T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141324436 | ||||||
| chr7:141324437
|
T | G | 19 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(16): Show | 19 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.496+111733T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141324437 | ||||||
| chr7:141324441
|
T | G | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+111737T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141324441 | ||||||
| chr7:141324442
|
T | G | 4 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(1): Show | 4 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+111738T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141324442 | ||||||
| chr7:141324443
|
T | G | 14 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(11): Show | 14 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.496+111739T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141324443 | ||||||
| chr7:141324567
|
C | T | 4 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(1): Show | 4 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+111863C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141324567 | ||||||
| chr7:141324644
|
G | A | 22 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(19): Show | 22 | HG00544.hp2 HG01255.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.496+111940G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141324644 | ||||||
| chr7:141324980
|
A | T | 2 | a0001c0001t0006g0025a0001c0002t0006g0040 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.496+112276A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141324980 | ||||||
| chr7:141325047
|
C | T | 4 | a0001c0002t0013g0047a0001c0002t0031g0063a0001c0002t0032g0071others(1): Show | 4 | HG00544.hp2 HG01255.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+112343C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141325047 | ||||||
| chr7:141325051
|
C | T | 22 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(19): Show | 22 | HG00544.hp2 HG01255.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.496+112347C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141325051 | ||||||
| chr7:141325214
|
G | T | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-112394G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141325214 | ||||||
| chr7:141325473
|
G | A | 13 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.497-112135G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141325473 | ||||||
| chr7:141325618
|
G | A | 2 | a0001c0002t0016g0072a0002c0006t0039g0061 | 2 | HG01261.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.497-111990G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141325618 | ||||||
| chr7:141325620
|
G | A | 1 | a0001c0003t0018g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.497-111988G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141325620 | ||||||
| chr7:141325657
|
T | C | 3 | a0001c0001t0006g0025a0001c0002t0006g0040a0001c0002t0017g0062 | 3 | HG02630.hp2 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.497-111951T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141325657 | ||||||
| chr7:141325823
|
GA | G | 47 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(44): Show | 47 | HG01106.hp2 HG01243.hp1 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.497-111775delA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141325823 | |||||
| chr7:141325839
|
A | C | 24 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(21): Show | 24 | HG00544.hp2 HG01255.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.497-111769A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141325839 | ||||||
| chr7:141325886
|
G | T | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.497-111722G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141325886 | ||||||
| chr7:141325913
|
T | G | 30 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(27): Show | 30 | HG00544.hp2 HG01243.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.497-111695T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141325913 | ||||||
| chr7:141326029
|
A | G | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-111579A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141326029 | ||||||
| chr7:141326054
|
C | T | 21 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0008g0030others(18): Show | 21 | HG00544.hp2 HG01255.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.497-111554C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141326054 | ||||||
| chr7:141326400
|
T | C | 56 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(53): Show | 56 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.497-111208T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141326400 | ||||||
| chr7:141326433
|
A | G | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-111175A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141326433 | ||||||
| chr7:141326765
|
A | G | 22 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(19): Show | 22 | HG00544.hp2 HG01255.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.497-110843A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141326765 | ||||||
| chr7:141326786
|
C | T | 1 | a0001c0001t0004g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.497-110822C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141326786 | ||||||
| chr7:141326861
|
G | A | 35 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0023others(32): Show | 35 | HG00544.hp2 HG01243.hp2 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.497-110747G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141326861 | ||||||
| chr7:141326960
|
A | T | 22 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(19): Show | 22 | HG00544.hp2 HG01255.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.497-110648A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141326960 | ||||||
| chr7:141327150
|
C | A | 1 | a0001c0001t0004g0023 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.497-110458C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141327150 | ||||||
| chr7:141327188
|
T | C | 1 | a0001c0002t0003g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.497-110420T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141327188 | ||||||
| chr7:141327258
|
C | T | 22 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(19): Show | 22 | HG00544.hp2 HG01255.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.497-110350C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141327258 | ||||||
| chr7:141327478
|
A | T | 22 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(19): Show | 22 | HG00544.hp2 HG01255.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.497-110130A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141327478 | ||||||
| chr7:141327513
|
G | T | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.497-110095G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141327513 | ||||||
| chr7:141327782
|
A | C | 56 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(53): Show | 56 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.497-109826A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141327782 | ||||||
| chr7:141327917
|
G | A | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-109691G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141327917 | ||||||
| chr7:141328134
|
G | C | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.497-109474G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141328134 | ||||||
| chr7:141328584
|
G | A | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-109024G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141328584 | ||||||
| chr7:141328643
|
C | T | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-108965C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141328643 | ||||||
| chr7:141328801
|
C | T | 1 | a0001c0002t0001g0057 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.497-108807C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141328801 | ||||||
| chr7:141328917
|
GTAAT | G | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-108682_497-108 others(10): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141328917 | |||||
| chr7:141328946
|
T | C | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-108662T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141328946 | ||||||
| chr7:141329023
|
G | A | 29 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(26): Show | 29 | HG00544.hp2 HG01243.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.497-108585G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141329023 | ||||||
| chr7:141329034
|
C | T | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-108574C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141329034 | ||||||
| chr7:141329070
|
A | G | 1 | a0001c0001t0003g0007 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.497-108538A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141329070 | ||||||
| chr7:141329078
|
A | G | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-108530A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141329078 | ||||||
| chr7:141329156
|
T | C | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-108452T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141329156 | ||||||
| chr7:141329180
|
A | C | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-108428A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141329180 | ||||||
| chr7:141329200
|
A | G | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-108408A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141329200 | ||||||
| chr7:141329471
|
T | G | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-108137T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141329471 | ||||||
| chr7:141329826
|
A | G | 4 | a0001c0002t0013g0047a0001c0002t0031g0063a0001c0002t0032g0071others(1): Show | 4 | HG00544.hp2 HG01255.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-107782A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141329826 | ||||||
| chr7:141330084
|
CT | C | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-107514delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141330084 | |||||
| chr7:141330429
|
T | C | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-107179T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141330429 | ||||||
| chr7:141330448
|
C | G | 1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.497-107160C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141330448 | ||||||
| chr7:141330589
|
C | T | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-107019C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141330589 | ||||||
| chr7:141330752
|
C | A | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-106856C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141330752 | ||||||
| chr7:141330910
|
A | C | 4 | a0001c0002t0013g0047a0001c0002t0031g0063a0001c0002t0032g0071others(1): Show | 4 | HG00544.hp2 HG01255.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-106698A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141330910 | ||||||
| chr7:141330997
|
C | G | 19 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(16): Show | 19 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.497-106611C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141330997 | ||||||
| chr7:141331175
|
A | G | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-106433A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141331175 | ||||||
| chr7:141331335
|
C | G | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-106273C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141331335 | ||||||
| chr7:141331353
|
G | A | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-106255G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141331353 | ||||||
| chr7:141331740
|
T | C | 19 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(16): Show | 19 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.497-105868T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141331740 | ||||||
| chr7:141332126
|
G | T | 6 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0008g0004others(3): Show | 6 | HG02486.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-105482G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141332126 | ||||||
| chr7:141332260
|
C | G | 6 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0008g0004others(3): Show | 6 | HG02486.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-105348C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141332260 | ||||||
| chr7:141332963
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.497-104645G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141332963 | ||||||
| chr7:141333210
|
G | A | 19 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(16): Show | 19 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.497-104398G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141333210 | ||||||
| chr7:141333391
|
A | G | 1 | a0001c0003t0018g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.497-104217A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141333391 | ||||||
| chr7:141333598
|
C | T | 1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.497-104010C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141333598 | ||||||
| chr7:141333639
|
G | A | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-103969G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141333639 | ||||||
| chr7:141333738
|
T | C | 20 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(17): Show | 20 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.497-103870T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141333738 | ||||||
| chr7:141333951
|
C | T | 13 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.497-103657C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141333951 | ||||||
| chr7:141333988
|
G | A | 18 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-103620G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141333988 | ||||||
| chr7:141334046
|
A | C | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-103562A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141334046 | ||||||
| chr7:141334234
|
C | T | 1 | a0001c0002t0037g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.497-103374C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141334234 | ||||||
| chr7:141334392
|
T | C | 23 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0006g0025others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.497-103216T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141334392 | ||||||
| chr7:141334403
|
G | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.497-103205G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141334403 | ||||||
| chr7:141334420
|
T | C | 1 | a0001c0002t0011g0044 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.497-103188T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141334420 | ||||||
| chr7:141334429
|
C | T | 1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.497-103179C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141334429 | ||||||
| chr7:141334468
|
A | G | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-103140A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141334468 | ||||||
| chr7:141334504
|
A | T | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-103104A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141334504 | ||||||
| chr7:141334863
|
C | G | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-102745C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141334863 | ||||||
| chr7:141335110
|
A | G | 1 | a0001c0001t0005g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.497-102498A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141335110 | ||||||
| chr7:141335226
|
T | C | 56 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(53): Show | 56 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.497-102382T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141335226 | ||||||
| chr7:141335294
|
C | T | 2 | a0001c0001t0004g0024a0001c0002t0005g0049 | 2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.497-102314C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141335294 | ||||||
| chr7:141335392
|
A | C | 15 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0008g0004others(12): Show | 15 | HG00544.hp2 HG01243.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.497-102216A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141335392 | ||||||
| chr7:141335396
|
C | T | 1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.497-102212C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141335396 | ||||||
| chr7:141335423
|
G | A | 4 | a0001c0002t0013g0047a0001c0002t0031g0063a0001c0002t0032g0071others(1): Show | 4 | HG00544.hp2 HG01255.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-102185G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141335423 | ||||||
| chr7:141335561
|
G | A | 15 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0008g0004others(12): Show | 15 | HG00544.hp2 HG01243.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.497-102047G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141335561 | ||||||
| chr7:141335775
|
G | A | 16 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0010g0021others(13): Show | 16 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.497-101833G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141335775 | ||||||
| chr7:141336132
|
C | T | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-101476C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141336132 | ||||||
| chr7:141336133
|
G | T | 2 | a0001c0001t0006g0025a0001c0002t0006g0040 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.497-101475G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141336133 | ||||||
| chr7:141336231
|
G | A | 12 | a0001c0001t0003g0020a0001c0001t0004g0029a0001c0001t0014g0033others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.497-101377G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141336231 | ||||||
| chr7:141336726
|
A | G | 3 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0002t0040g0050 | 3 | HG02922.hp2 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.497-100882A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141336726 | ||||||
| chr7:141336850
|
T | C | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-100758T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141336850 | ||||||
| chr7:141336851
|
A | ACCATCAC others(447): Show |
1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-100750_497-100 others(460): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141336851 | |||||
| chr7:141336909
|
T | TCATCACC others(17): Show |
1 | a0001c0002t0015g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.497-100697_497-100 others(30): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141336909 | |||||
| chr7:141336909
|
TCAC | T | 8 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0011g0044others(5): Show | 8 | HG00544.hp2 HG01255.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.497-100678_497-100 others(9): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141336909 | |||||
| chr7:141336918
|
C | CCACCACC others(17): Show |
21 | a0001c0001t0001g0015a0001c0001t0003g0007a0001c0001t0003g0020others(18): Show | 21 | HG01243.hp1 HG01884.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.497-100679_497-100 others(30): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141336918 | |||||
| chr7:141336918
|
C | CCACCACC others(59): Show |
1 | a0001c0001t0001g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.497-100679_497-100 others(72): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141336918 | |||||
| chr7:141336918
|
C | T | 1 | a0001c0002t0015g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.497-100690C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141336918 | ||||||
| chr7:141336933
|
T | C | 23 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(20): Show | 23 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.497-100675T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141336933 | ||||||
| chr7:141336954
|
C | T | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-100654C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141336954 | ||||||
| chr7:141336956
|
A | C | 1 | a0001c0001t0034g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.497-100652A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141336956 | ||||||
| chr7:141336960
|
T | C | 4 | a0001c0002t0011g0044a0001c0002t0013g0047a0001c0002t0032g0071others(1): Show | 4 | HG00544.hp2 HG01255.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-100648T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141336960 | ||||||
| chr7:141336964
|
T | C | 7 | a0001c0001t0014g0033a0001c0001t0014g0039a0001c0001t0028g0022others(4): Show | 7 | HG00544.hp2 HG01243.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.497-100644T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141336964 | ||||||
| chr7:141336967
|
C | CACCACCA others(278): Show |
1 | a0001c0002t0005g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.497-100568_497-100 others(291): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141336967 | |||||
| chr7:141336967
|
C | CACCACCA others(431): Show |
1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.497-100568_497-100 others(444): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141336967 | |||||
| chr7:141336975
|
C | CCACCACC others(2): Show |
2 | a0001c0002t0001g0048a0001c0002t0001g0065 | 2 | HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.497-100626_497-100 others(15): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141336975 | |||||
| chr7:141336983
|
C | A | 28 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(25): Show | 28 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.497-100625C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141336983 | ||||||
| chr7:141336991
|
T | C | 24 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(21): Show | 24 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.497-100617T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141336991 | ||||||
| chr7:141336996
|
T | C | 27 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(24): Show | 27 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.497-100612T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141336996 | ||||||
| chr7:141336996
|
T | TCACCACC others(5): Show |
1 | a0001c0001t0034g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.497-100610_497-100 others(18): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141336996 | |||||
| chr7:141336999
|
T | C | 6 | a0001c0002t0001g0048a0001c0002t0001g0065a0001c0002t0011g0044others(3): Show | 6 | HG00544.hp2 HG01255.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-100609T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141336999 | ||||||
| chr7:141336999
|
T | TCACCACC others(5): Show |
21 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(18): Show | 21 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.497-100607_497-100 others(18): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141336999 | |||||
| chr7:141337002
|
T | C | 7 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0011g0044others(4): Show | 7 | HG00544.hp2 HG01255.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.497-100606T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337002 | ||||||
| chr7:141337008
|
C | CCACCACC others(137): Show |
1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-100585_497-100 others(150): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337008 | |||||
| chr7:141337014
|
C | T | 3 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.497-100594C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337014 | ||||||
| chr7:141337017
|
T | C | 4 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0001t0034g0009others(1): Show | 4 | HG02572.hp1 HG02647.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-100591T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337017 | ||||||
| chr7:141337017
|
T | TCACCACC others(239): Show |
1 | a0001c0003t0019g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497-100568_497-100 others(252): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337017 | |||||
| chr7:141337026
|
T | C | 26 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(23): Show | 26 | HG01106.hp2 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.497-100582T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337026 | ||||||
| chr7:141337026
|
T | TCACCACC others(470): Show |
1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.497-100568_497-100 others(483): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337026 | |||||
| chr7:141337026
|
T | TCACCACC others(548): Show |
1 | a0001c0001t0001g0035 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.497-100568_497-100 others(561): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337026 | |||||
| chr7:141337026
|
T | TCACCACC others(338): Show |
3 | a0001c0001t0004g0023a0001c0001t0010g0021a0001c0002t0042g0054 | 3 | HG01952.hp2 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.497-100568_497-100 others(351): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337026 | |||||
| chr7:141337038
|
C | CCACCAT | 22 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(19): Show | 22 | HG01106.hp2 HG01243.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.497-100565_497-100 others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337038 | |||||
| chr7:141337038
|
C | CCACCATC others(191): Show |
1 | a0001c0003t0001g0068 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.497-100565_497-100 others(204): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337038 | |||||
| chr7:141337038
|
C | CCATCACC others(32): Show |
1 | a0001c0002t0011g0044 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.497-100568_497-100 others(45): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337038 | |||||
| chr7:141337038
|
C | CCATCACC others(206): Show |
2 | a0001c0002t0013g0047a0001c0002t0032g0071 | 2 | HG00544.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.497-100568_497-100 others(219): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337038 | |||||
| chr7:141337038
|
C | CCATCACC others(722): Show |
1 | a0001c0005t0001g0005 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.497-100568_497-100 others(735): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337038 | |||||
| chr7:141337038
|
C | CCATCACT others(53): Show |
3 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.497-100568_497-100 others(66): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337038 | |||||
| chr7:141337038
|
C | CCATCAT | 2 | a0001c0001t0004g0029a0001c0002t0037g0075 | 2 | HG02027.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.497-100568_497-100 others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337038 | |||||
| chr7:141337038
|
C | CCATCATC others(224): Show |
2 | a0001c0002t0001g0064a0001c0002t0007g0053 | 2 | HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.497-100568_497-100 others(237): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337038 | |||||
| chr7:141337038
|
C | CCATCATC others(218): Show |
1 | a0001c0002t0001g0057 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.497-100568_497-100 others(231): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337038 | |||||
| chr7:141337038
|
C | CCATCATC others(1019): Show |
1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.497-100568_497-100 others(1032): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337038 | |||||
| chr7:141337038
|
C | CCATCATC others(593): Show |
2 | a0001c0001t0005g0008a0001c0001t0023g0018 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-100568_497-100 others(606): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337038 | |||||
| chr7:141337038
|
C | CCATCATC others(236): Show |
1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-100568_497-100 others(249): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337038 | |||||
| chr7:141337038
|
C | CCATCATC others(23): Show |
2 | a0001c0001t0021g0077a0001c0002t0027g0051 | 2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.497-100568_497-100 others(36): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337038 | |||||
| chr7:141337038
|
C | T | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-100570C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337038 | ||||||
| chr7:141337041
|
C | T | 11 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(8): Show | 11 | HG01891.hp1 HG01891.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.497-100567C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337041 | ||||||
| chr7:141337044
|
C | T | 6 | a0001c0001t0008g0030a0001c0001t0016g0037a0001c0002t0002g0043others(3): Show | 6 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-100564C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337044 | ||||||
| chr7:141337047
|
C | G | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-100561C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337047 | ||||||
| chr7:141337047
|
C | T | 4 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0002t0011g0044others(1): Show | 4 | HG02083.hp1 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-100561C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337047 | ||||||
| chr7:141337050
|
T | C | 15 | a0001c0001t0001g0035a0001c0001t0004g0029a0001c0001t0005g0008others(12): Show | 15 | HG01891.hp1 HG01891.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.497-100558T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337050 | ||||||
| chr7:141337053
|
C | CCACCACC others(206): Show |
1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.497-100544_497-100 others(219): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337053 | |||||
| chr7:141337056
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.497-100552C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337056 | ||||||
| chr7:141337059
|
C | T | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-100549C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337059 | ||||||
| chr7:141337065
|
T | C | 11 | a0001c0001t0001g0035a0001c0001t0004g0029a0001c0001t0016g0037others(8): Show | 11 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-100543T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337065 | ||||||
| chr7:141337068
|
C | T | 3 | a0001c0001t0004g0023a0001c0001t0010g0021a0001c0002t0042g0054 | 3 | HG01952.hp2 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.497-100540C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337068 | ||||||
| chr7:141337069
|
T | C | 18 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0023others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-100539T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337069 | ||||||
| chr7:141337069
|
T | TACC | 34 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(31): Show | 34 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.497-100526_497-100 others(9): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337069 | |||||
| chr7:141337071
|
C | T | 2 | a0001c0001t0004g0029a0001c0001t0033g0031 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.497-100537C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337071 | ||||||
| chr7:141337074
|
C | T | 4 | a0001c0001t0016g0037a0001c0002t0002g0043a0001c0002t0003g0052others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-100534C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337074 | ||||||
| chr7:141337075
|
C | G | 1 | a0001c0003t0019g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497-100533C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337075 | ||||||
| chr7:141337077
|
C | T | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.497-100531C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337077 | ||||||
| chr7:141337083
|
C | T | 3 | a0001c0001t0021g0077a0001c0001t0034g0009a0001c0002t0027g0051 | 3 | HG03130.hp1 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.497-100525C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337083 | ||||||
| chr7:141337084
|
C | CACCACCA others(395): Show |
1 | a0001c0002t0037g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.497-100524_497-100 others(408): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337084 | ||||||
| chr7:141337085
|
C | A | 24 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0023others(21): Show | 24 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.497-100523C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337085 | ||||||
| chr7:141337086
|
C | G | 1 | a0001c0003t0019g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497-100522C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337086 | ||||||
| chr7:141337089
|
T | C | 19 | a0001c0001t0002g0019a0001c0001t0004g0023a0001c0001t0004g0029others(16): Show | 19 | HG01891.hp1 HG01891.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.497-100519T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337089 | ||||||
| chr7:141337093
|
T | C | 24 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0023others(21): Show | 24 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.497-100515T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337093 | ||||||
| chr7:141337098
|
T | C | 17 | a0001c0001t0001g0035a0001c0001t0004g0029a0001c0001t0005g0008others(14): Show | 17 | HG01891.hp1 HG01891.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.497-100510T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337098 | ||||||
| chr7:141337101
|
T | C | 14 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0023others(11): Show | 14 | HG01891.hp1 HG01891.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.497-100507T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337101 | ||||||
| chr7:141337101
|
T | G | 3 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0002t0040g0050 | 3 | HG02922.hp2 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.497-100507T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337101 | ||||||
| chr7:141337101
|
T | TCAC | 2 | a0001c0001t0021g0077a0001c0002t0027g0051 | 2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.497-100505_497-100 others(9): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337101 | |||||
| chr7:141337104
|
T | C | 17 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0023others(14): Show | 17 | HG01884.hp1 HG01952.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.497-100504T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337104 | ||||||
| chr7:141337110
|
C | CCAGCATC others(326): Show |
1 | a0001c0001t0034g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.497-100496_497-100 others(339): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337110 | |||||
| chr7:141337113
|
C | T | 3 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0002t0040g0050 | 3 | HG02922.hp2 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.497-100495C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337113 | ||||||
| chr7:141337114
|
C | G | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.497-100494C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337114 | ||||||
| chr7:141337119
|
T | C | 14 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0023others(11): Show | 14 | HG01952.hp2 HG02109.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-100489T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337119 | ||||||
| chr7:141337122
|
C | T | 3 | a0001c0001t0016g0037a0001c0002t0002g0043a0001c0002t0003g0052 | 3 | HG01891.hp1 HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.497-100486C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337122 | ||||||
| chr7:141337123
|
C | T | 2 | a0001c0002t0037g0075a0001c0003t0019g0070 | 2 | HG01884.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.497-100485C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337123 | ||||||
| chr7:141337125
|
C | G | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.497-100483C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337125 | ||||||
| chr7:141337128
|
T | C | 10 | a0001c0001t0001g0035a0001c0001t0004g0029a0001c0001t0016g0037others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.497-100480T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337128 | ||||||
| chr7:141337131
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.497-100477C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337131 | ||||||
| chr7:141337134
|
C | CCATCACC others(191): Show |
1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.497-100472_497-100 others(204): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337134 | |||||
| chr7:141337137
|
C | T | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-100471C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337137 | ||||||
| chr7:141337140
|
C | CCACCACC others(1109): Show |
1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-100466_497-100 others(1122): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337140 | |||||
| chr7:141337143
|
T | C | 35 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(32): Show | 35 | HG00544.hp1 HG01106.hp1 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.497-100465T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337143 | ||||||
| chr7:141337146
|
T | C | 36 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0080others(33): Show | 36 | HG00544.hp1 HG01106.hp1 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.497-100462T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337146 | ||||||
| chr7:141337150
|
C | T | 1 | a0001c0001t0034g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.497-100458C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337150 | ||||||
| chr7:141337152
|
C | CCACCACC others(191): Show |
1 | a0001c0002t0010g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(204): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337152 | |||||
| chr7:141337152
|
C | CCATCACC others(200): Show |
3 | a0001c0001t0016g0037a0001c0002t0002g0043a0001c0002t0003g0052 | 3 | HG01891.hp1 HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.497-100454_497-100 others(213): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337152 | |||||
| chr7:141337152
|
C | T | 18 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0004g0024others(15): Show | 18 | HG00544.hp1 HG01106.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-100456C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337152 | ||||||
| chr7:141337153
|
C | CACCACCA others(353): Show |
3 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.497-100451_497-100 others(366): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337153 | |||||
| chr7:141337153
|
C | CACCACCA others(332): Show |
1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(345): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337153 | |||||
| chr7:141337155
|
C | T | 2 | a0001c0002t0037g0075a0001c0003t0019g0070 | 2 | HG01884.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.497-100453C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337155 | ||||||
| chr7:141337156
|
C | CACCACCA others(1517): Show |
1 | a0001c0001t0003g0007 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(1530): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1175): Show |
1 | a0001c0002t0013g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(1188): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(833): Show |
3 | a0001c0001t0003g0020a0001c0001t0035g0079a0001c0002t0009g0060 | 3 | HG02258.hp1 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.497-100451_497-100 others(846): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1229): Show |
1 | a0001c0001t0001g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(1242): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1520): Show |
1 | a0001c0001t0012g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(1533): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1220): Show |
1 | a0001c0001t0020g0006 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(1233): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1271): Show |
1 | a0001c0002t0007g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(1284): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1286): Show |
1 | a0001c0001t0011g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(1299): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1340): Show |
1 | a0001c0001t0001g0015 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(1353): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1271): Show |
1 | a0001c0001t0038g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(1284): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1256): Show |
1 | a0001c0001t0014g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(1269): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1253): Show |
2 | a0001c0001t0029g0026a0001c0002t0001g0076 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.497-100451_497-100 others(1266): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1223): Show |
1 | a0001c0001t0014g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(1236): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1238): Show |
1 | a0001c0001t0028g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(1251): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1271): Show |
2 | a0001c0002t0001g0048a0001c0002t0001g0065 | 2 | HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.497-100451_497-100 others(1284): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(830): Show |
1 | a0001c0002t0015g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(843): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1130): Show |
1 | a0001c0002t0032g0071 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(1143): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1127): Show |
1 | a0001c0005t0001g0005 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(1140): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1283): Show |
1 | a0001c0001t0006g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(1296): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(395): Show |
1 | a0001c0003t0001g0068 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(408): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(581): Show |
1 | a0001c0002t0001g0057 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(594): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(422): Show |
1 | a0001c0002t0007g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(435): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1475): Show |
1 | a0001c0001t0007g0011 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(1488): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(392): Show |
1 | a0001c0002t0001g0064 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(405): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(2270): Show |
1 | a0001c0002t0031g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(2283): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1856): Show |
1 | a0001c0002t0013g0059 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(1869): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1820): Show |
1 | a0001c0002t0036g0069 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(1833): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1466): Show |
1 | a0001c0002t0024g0002 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(1479): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(650): Show |
2 | a0001c0001t0015g0028a0001c0002t0008g0003 | 2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.497-100451_497-100 others(663): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(710): Show |
1 | a0001c0001t0004g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(723): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1739): Show |
1 | a0001c0003t0018g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(1752): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1595): Show |
1 | a0001c0003t0001g0074 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(1608): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1595): Show |
1 | a0001c0001t0001g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(1608): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(356): Show |
1 | a0001c0001t0022g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(369): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1604): Show |
1 | a0001c0003t0001g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(1617): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(602): Show |
1 | a0001c0002t0016g0072 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(615): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(659): Show |
1 | a0002c0006t0039g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(672): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1364): Show |
1 | a0001c0002t0041g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(1377): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1595): Show |
1 | a0001c0001t0001g0038 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(1608): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(1676): Show |
1 | a0001c0002t0012g0045 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(1689): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CACCACCA others(938): Show |
1 | a0001c0001t0005g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.497-100451_497-100 others(951): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337156
|
C | CAGCATCA others(305): Show |
1 | a0001c0002t0011g0044 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.497-100451_497-100 others(318): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337156 | |||||
| chr7:141337158
|
T | C | 66 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(63): Show | 66 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.497-100450T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337158 | ||||||
| chr7:141337158
|
T | G | 3 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0002t0040g0050 | 3 | HG02922.hp2 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.497-100450T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337158 | ||||||
| chr7:141337158
|
T | TCACCACC others(620): Show |
1 | a0001c0002t0005g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.497-100436_497-100 others(633): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337158 | |||||
| chr7:141337158
|
T | TCACCACC others(599): Show |
1 | a0001c0001t0002g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.497-100436_497-100 others(612): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337158 | |||||
| chr7:141337158
|
T | TCACCACC others(611): Show |
1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.497-100436_497-100 others(624): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337158 | |||||
| chr7:141337158
|
T | TCACCACC others(254): Show |
2 | a0001c0001t0021g0077a0001c0002t0027g0051 | 2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.497-100436_497-100 others(267): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337158 | |||||
| chr7:141337158
|
T | TCACCACC others(224): Show |
1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.497-100436_497-100 others(237): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337158 | |||||
| chr7:141337159
|
C | CACCACCA others(1460): Show |
2 | a0001c0001t0006g0025a0001c0002t0006g0040 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.497-100433_497-100 others(1473): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337159 | |||||
| chr7:141337161
|
C | T | 2 | a0001c0001t0008g0030a0001c0004t0043g0032 | 2 | HG02109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.497-100447C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337161 | ||||||
| chr7:141337162
|
C | T | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-100446C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337162 | ||||||
| chr7:141337165
|
C | CACCATCA others(464): Show |
3 | a0001c0001t0004g0023a0001c0001t0010g0021a0001c0002t0042g0054 | 3 | HG01952.hp2 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.497-100439_497-100 others(477): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337165 | |||||
| chr7:141337165
|
C | T | 2 | a0001c0001t0008g0030a0001c0004t0043g0032 | 2 | HG02109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.497-100443C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337165 | ||||||
| chr7:141337167
|
C | CCAT | 3 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0002t0040g0050 | 3 | HG02922.hp2 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.497-100439_497-100 others(9): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337167 | |||||
| chr7:141337170
|
C | T | 2 | a0001c0002t0037g0075a0001c0003t0019g0070 | 2 | HG01884.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.497-100438C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337170 | ||||||
| chr7:141337171
|
C | T | 3 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0002t0040g0050 | 3 | HG02922.hp2 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.497-100437C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337171 | ||||||
| chr7:141337185
|
G | C | 15 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0023others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.497-100423G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337185 | ||||||
| chr7:141337185
|
G | T | 2 | a0001c0001t0004g0029a0001c0001t0033g0031 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.497-100423G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337185 | ||||||
| chr7:141337191
|
C | T | 2 | a0001c0002t0037g0075a0001c0003t0019g0070 | 2 | HG01884.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.497-100417C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337191 | ||||||
| chr7:141337197
|
T | C | 5 | a0001c0001t0001g0035a0001c0001t0004g0029a0001c0001t0033g0031others(2): Show | 5 | HG01884.hp1 HG02027.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-100411T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337197 | ||||||
| chr7:141337206
|
C | CCACCACC others(749): Show |
1 | a0001c0001t0033g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.497-100397_497-100 others(762): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337206 | |||||
| chr7:141337206
|
C | CCACCACC others(746): Show |
1 | a0001c0001t0004g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.497-100397_497-100 others(759): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337206 | |||||
| chr7:141337212
|
T | C | 4 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0029others(1): Show | 4 | HG02630.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-100396T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337212 | ||||||
| chr7:141337212
|
TCAC | T | 5 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0026g0041others(2): Show | 5 | HG01255.hp1 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.497-100376_497-100 others(9): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337212 | |||||
| chr7:141337215
|
C | CCACCACC others(50): Show |
1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.497-100385_497-100 others(63): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337215 | |||||
| chr7:141337215
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.497-100393C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337215 | ||||||
| chr7:141337218
|
C | CCACCACC others(59): Show |
1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.497-100382_497-100 others(72): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141337218 | |||||
| chr7:141337271
|
C | T | 13 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.497-100337C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337271 | ||||||
| chr7:141337318
|
T | A | 77 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(74): Show | 77 | HG00544.hp1 HG00544.hp2 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.497-100290T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337318 | ||||||
| chr7:141337534
|
A | T | 1 | a0001c0001t0034g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.497-100074A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337534 | ||||||
| chr7:141337562
|
G | C | 2 | a0001c0001t0004g0029a0001c0001t0033g0031 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.497-100046G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141337562 | ||||||
| chr7:141338027
|
T | C | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-99581T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141338027 | ||||||
| chr7:141338078
|
G | C | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-99530G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141338078 | ||||||
| chr7:141338091
|
C | G | 2 | a0001c0001t0021g0077a0001c0002t0027g0051 | 2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.497-99517C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141338091 | ||||||
| chr7:141338416
|
G | A | 8 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(5): Show | 8 | HG02109.hp1 HG02486.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.497-99192G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141338416 | ||||||
| chr7:141338912
|
C | T | 57 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(54): Show | 57 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.497-98696C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141338912 | ||||||
| chr7:141339290
|
T | C | 27 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(24): Show | 27 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.497-98318T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141339290 | ||||||
| chr7:141339383
|
C | G | 80 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(77): Show | 80 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.497-98225C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141339383 | ||||||
| chr7:141339433
|
C | T | 4 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(1): Show | 4 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-98175C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141339433 | ||||||
| chr7:141339491
|
C | T | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-98117C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141339491 | ||||||
| chr7:141339558
|
C | T | 10 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(7): Show | 10 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-98050C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141339558 | ||||||
| chr7:141339580
|
G | A | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-98028G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141339580 | ||||||
| chr7:141339608
|
T | C | 10 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(7): Show | 10 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-98000T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141339608 | ||||||
| chr7:141339802
|
G | A | 14 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(11): Show | 14 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.497-97806G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141339802 | ||||||
| chr7:141339834
|
A | G | 9 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(6): Show | 9 | HG02486.hp1 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.497-97774A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141339834 | ||||||
| chr7:141340038
|
C | T | 3 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0001t0025g0010 | 3 | HG02486.hp1 HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-97570C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141340038 | ||||||
| chr7:141340098
|
T | C | 1 | a0001c0002t0001g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.497-97510T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141340098 | ||||||
| chr7:141340382
|
G | A | 59 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(56): Show | 59 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.497-97226G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141340382 | ||||||
| chr7:141340440
|
GTTA | G | 5 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0008g0004others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.497-97163_497-9716 others(7): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141340440 | |||||
| chr7:141340562
|
G | T | 6 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0008g0004others(3): Show | 6 | HG02572.hp1 HG02647.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-97046G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141340562 | ||||||
| chr7:141340727
|
A | C | 1 | a0001c0002t0002g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.497-96881A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141340727 | ||||||
| chr7:141340835
|
G | A | 5 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0008g0004others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.497-96773G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141340835 | ||||||
| chr7:141341671
|
G | A | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-95937G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141341671 | ||||||
| chr7:141341727
|
A | C | 1 | a0001c0001t0001g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.497-95881A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141341727 | ||||||
| chr7:141341753
|
A | G | 1 | a0001c0001t0038g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.497-95855A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141341753 | ||||||
| chr7:141341754
|
GA | G | 5 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0001t0025g0010others(2): Show | 5 | HG02083.hp2 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-95843delA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141341754 | |||||
| chr7:141341763
|
A | T | 1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.497-95845A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141341763 | ||||||
| chr7:141342000
|
T | G | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-95608T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141342000 | ||||||
| chr7:141342148
|
A | T | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-95460A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141342148 | ||||||
| chr7:141342188
|
T | C | 4 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0001t0025g0010others(1): Show | 4 | HG02109.hp1 HG02486.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-95420T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141342188 | ||||||
| chr7:141342323
|
G | A | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-95285G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141342323 | ||||||
| chr7:141342379
|
T | C | 4 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0001t0025g0010others(1): Show | 4 | HG02109.hp1 HG02486.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-95229T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141342379 | ||||||
| chr7:141342516
|
C | T | 16 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(13): Show | 16 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.497-95092C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141342516 | ||||||
| chr7:141342693
|
G | C | 2 | a0001c0001t0006g0025a0001c0002t0006g0040 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.497-94915G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141342693 | ||||||
| chr7:141343525
|
C | CT | 38 | a0001c0001t0001g0012a0001c0001t0002g0027a0001c0001t0003g0007others(35): Show | 38 | HG00544.hp2 HG01106.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.497-94059dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141343525 | |||||
| chr7:141343525
|
C | CTT | 8 | a0001c0001t0001g0015a0001c0001t0004g0023a0001c0001t0014g0033others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.497-94060_497-9405 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141343525 | |||||
| chr7:141343525
|
CT | C | 4 | a0001c0001t0001g0035a0001c0001t0005g0008a0001c0001t0023g0018others(1): Show | 4 | HG02897.hp2 HG02922.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-94059delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141343525 | |||||
| chr7:141343525
|
CTT | C | 6 | a0001c0001t0002g0019a0001c0001t0008g0004a0001c0001t0009g0078others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-94060_497-9405 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141343525 | |||||
| chr7:141343545
|
T | G | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-94063T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141343545 | ||||||
| chr7:141343641
|
A | G | 51 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(48): Show | 51 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.497-93967A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141343641 | ||||||
| chr7:141343698
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.497-93910C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141343698 | ||||||
| chr7:141343957
|
G | C | 1 | a0001c0002t0012g0045 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.497-93651G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141343957 | ||||||
| chr7:141344054
|
G | A | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.497-93554G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141344054 | ||||||
| chr7:141344142
|
G | A | 4 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(1): Show | 4 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-93466G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141344142 | ||||||
| chr7:141344508
|
G | A | 5 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0008g0004others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.497-93100G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141344508 | ||||||
| chr7:141344544
|
T | TCTCC | 2 | a0001c0002t0017g0062a0001c0002t0042g0054 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.497-93051_497-9304 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141344544 | |||||
| chr7:141344559
|
CCATTCCT others(4): Show |
C | 6 | a0001c0001t0008g0030a0001c0001t0034g0009a0001c0002t0031g0063others(3): Show | 6 | HG01884.hp1 HG02027.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-93047_497-9303 others(15): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141344559 | |||||
| chr7:141344561
|
A | C | 2 | a0001c0001t0004g0023a0001c0001t0010g0021 | 2 | HG01952.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.497-93047A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141344561 | ||||||
| chr7:141344563
|
T | C | 2 | a0001c0001t0004g0023a0001c0001t0010g0021 | 2 | HG01952.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.497-93045T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141344563 | ||||||
| chr7:141344565
|
C | A | 2 | a0001c0001t0004g0023a0001c0001t0010g0021 | 2 | HG01952.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.497-93043C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141344565 | ||||||
| chr7:141344569
|
C | CTCCTCCC others(5): Show |
1 | a0001c0002t0002g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.497-93034_497-9302 others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141344569 | |||||
| chr7:141344574
|
C | CCCTT | 7 | a0001c0001t0001g0038a0001c0001t0008g0004a0001c0001t0009g0078others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.497-92982_497-9297 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141344574 | |||||
| chr7:141344574
|
C | CCCTTCCT others(1): Show |
5 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0028g0022others(2): Show | 5 | HG02897.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-92986_497-9297 others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141344574 | |||||
| chr7:141344574
|
C | CCCTTCCT others(9): Show |
2 | a0001c0001t0007g0011a0001c0003t0001g0074 | 2 | HG01106.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.497-92994_497-9297 others(20): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141344574 | |||||
| chr7:141344574
|
C | CCCTTCCT others(45): Show |
1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-92999_497-9299 others(56): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141344574 | |||||
| chr7:141344574
|
C | CCCTTCTT others(9): Show |
1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.497-93029_497-9302 others(20): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141344574 | |||||
| chr7:141344574
|
CCCTT | C | 26 | a0001c0001t0001g0015a0001c0001t0001g0080a0001c0001t0002g0027others(23): Show | 26 | HG00544.hp1 HG00544.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.497-92982_497-9297 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141344574 | |||||
| chr7:141344574
|
CCCTTCCT others(1): Show |
C | 15 | a0001c0001t0004g0024a0001c0001t0020g0006a0001c0001t0035g0079others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.497-92986_497-9297 others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141344574 | |||||
| chr7:141344574
|
CCCTTCCT others(5): Show |
C | 2 | a0001c0002t0016g0072a0002c0006t0039g0061 | 2 | HG01261.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.497-92990_497-9297 others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141344574 | |||||
| chr7:141344574
|
CCCTTCCT others(9): Show |
C | 2 | a0001c0001t0004g0029a0001c0001t0033g0031 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.497-92994_497-9297 others(20): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141344574 | |||||
| chr7:141344576
|
C | A | 6 | a0001c0001t0008g0030a0001c0001t0034g0009a0001c0002t0031g0063others(3): Show | 6 | HG01884.hp1 HG02027.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-93032C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141344576 | ||||||
| chr7:141344576
|
CT | C | 2 | a0001c0001t0004g0023a0001c0001t0010g0021 | 2 | HG01952.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.497-93030delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141344576 | |||||
| chr7:141344580
|
CTTCCT | C | 5 | a0001c0001t0008g0030a0001c0001t0034g0009a0001c0002t0031g0063others(2): Show | 5 | HG01884.hp1 HG02109.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.497-93026_497-9302 others(9): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141344580 | |||||
| chr7:141344582
|
T | C | 2 | a0001c0001t0004g0023a0001c0001t0010g0021 | 2 | HG01952.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.497-93026T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141344582 | ||||||
| chr7:141344585
|
T | C | 1 | a0001c0002t0037g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.497-93023T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141344585 | ||||||
| chr7:141344589
|
T | C | 5 | a0001c0001t0008g0030a0001c0001t0034g0009a0001c0002t0031g0063others(2): Show | 5 | HG01884.hp1 HG02109.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.497-93019T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141344589 | ||||||
| chr7:141344590
|
T | C | 1 | a0001c0002t0037g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.497-93018T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141344590 | ||||||
| chr7:141344594
|
T | C | 5 | a0001c0001t0008g0030a0001c0001t0034g0009a0001c0002t0031g0063others(2): Show | 5 | HG01884.hp1 HG02109.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.497-93014T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141344594 | ||||||
| chr7:141344610
|
T | C | 2 | a0001c0001t0005g0008a0001c0001t0044g0001 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.497-92998T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141344610 | ||||||
| chr7:141344634
|
T | C | 1 | a0001c0001t0034g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.497-92974T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141344634 | ||||||
| chr7:141345251
|
A | G | 2 | a0001c0001t0023g0018a0001c0002t0002g0043 | 2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-92357A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141345251 | ||||||
| chr7:141345381
|
T | C | 1 | a0001c0003t0019g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497-92227T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141345381 | ||||||
| chr7:141345502
|
C | T | 4 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-92106C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141345502 | ||||||
| chr7:141345503
|
G | A | 1 | a0001c0002t0015g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.497-92105G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141345503 | ||||||
| chr7:141345567
|
C | T | 3 | a0001c0001t0015g0028a0001c0001t0021g0077a0001c0002t0008g0003 | 3 | HG03471.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.497-92041C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141345567 | ||||||
| chr7:141345619
|
G | A | 4 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-91989G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141345619 | ||||||
| chr7:141345839
|
A | G | 1 | a0001c0002t0009g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.497-91769A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141345839 | ||||||
| chr7:141346005
|
G | C | 5 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-91603G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141346005 | ||||||
| chr7:141346024
|
A | C | 1 | a0001c0001t0034g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.497-91584A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141346024 | ||||||
| chr7:141346025
|
T | C | 1 | a0001c0001t0034g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.497-91583T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141346025 | ||||||
| chr7:141346026
|
C | T | 1 | a0001c0001t0034g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.497-91582C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141346026 | ||||||
| chr7:141346123
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0008g0004others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.497-91485A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141346123 | ||||||
| chr7:141346142
|
A | G | 1 | a0001c0001t0028g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.497-91466A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141346142 | ||||||
| chr7:141346232
|
C | CA | 5 | a0001c0001t0001g0080a0001c0002t0013g0047a0001c0002t0032g0071others(2): Show | 5 | HG00544.hp1 HG00544.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-91368dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141346232 | |||||
| chr7:141346241
|
C | A | 4 | a0001c0001t0001g0080a0001c0002t0013g0047a0001c0002t0032g0071others(1): Show | 4 | HG00544.hp1 HG00544.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-91367C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141346241 | ||||||
| chr7:141346456
|
T | C | 15 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(12): Show | 15 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.497-91152T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141346456 | ||||||
| chr7:141346563
|
C | T | 5 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-91045C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141346563 | ||||||
| chr7:141346585
|
G | A | 1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.497-91023G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141346585 | ||||||
| chr7:141346598
|
T | C | 1 | a0001c0002t0007g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.497-91010T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141346598 | ||||||
| chr7:141346643
|
C | A | 3 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016 | 3 | HG02258.hp2 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.497-90965C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141346643 | ||||||
| chr7:141346866
|
A | T | 5 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-90742A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141346866 | ||||||
| chr7:141347662
|
C | T | 1 | a0001c0002t0011g0044 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.497-89946C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141347662 | ||||||
| chr7:141347719
|
C | G | 1 | a0001c0001t0020g0006 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.497-89889C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141347719 | ||||||
| chr7:141348161
|
G | T | 15 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(12): Show | 15 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.497-89447G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141348161 | ||||||
| chr7:141348844
|
A | G | 5 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-88764A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141348844 | ||||||
| chr7:141348907
|
A | G | 3 | a0001c0001t0015g0028a0001c0001t0021g0077a0001c0002t0008g0003 | 3 | HG03471.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.497-88701A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141348907 | ||||||
| chr7:141348967
|
C | T | 1 | a0001c0002t0002g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.497-88641C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141348967 | ||||||
| chr7:141349103
|
T | C | 44 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0080others(41): Show | 44 | HG00544.hp1 HG00544.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.497-88505T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141349103 | ||||||
| chr7:141349123
|
A | G | 15 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(12): Show | 15 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.497-88485A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141349123 | ||||||
| chr7:141349224
|
T | G | 2 | a0001c0001t0038g0034a0001c0002t0040g0050 | 2 | HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.497-88384T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141349224 | ||||||
| chr7:141349277
|
T | C | 2 | a0001c0001t0005g0008a0001c0001t0044g0001 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.497-88331T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141349277 | ||||||
| chr7:141349299
|
A | G | 15 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(12): Show | 15 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.497-88309A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141349299 | ||||||
| chr7:141349681
|
A | G | 15 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(12): Show | 15 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.497-87927A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141349681 | ||||||
| chr7:141349878
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.497-87730C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141349878 | ||||||
| chr7:141349910
|
G | A | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.497-87698G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141349910 | ||||||
| chr7:141349955
|
G | GCATC | 4 | a0001c0001t0023g0018a0001c0002t0003g0052a0001c0002t0015g0056others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-87613_497-8761 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141349955 | |||||
| chr7:141349955
|
GCATCCAT others(5): Show |
G | 18 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0080others(15): Show | 18 | HG00544.hp1 HG00544.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.497-87621_497-8761 others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141349955 | |||||
| chr7:141350446
|
C | T | 1 | a0001c0002t0001g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.497-87162C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141350446 | ||||||
| chr7:141350452
|
G | A | 2 | a0001c0001t0005g0008a0001c0001t0044g0001 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.497-87156G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141350452 | ||||||
| chr7:141350719
|
C | T | 6 | a0001c0001t0034g0009a0001c0002t0013g0059a0001c0002t0031g0063others(3): Show | 6 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-86889C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141350719 | ||||||
| chr7:141350778
|
T | C | 3 | a0001c0001t0004g0023a0001c0001t0010g0021a0001c0002t0042g0054 | 3 | HG01952.hp2 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.497-86830T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141350778 | ||||||
| chr7:141350891
|
A | G | 5 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-86717A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141350891 | ||||||
| chr7:141351215
|
T | C | 15 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(12): Show | 15 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.497-86393T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141351215 | ||||||
| chr7:141351273
|
A | G | 5 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-86335A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141351273 | ||||||
| chr7:141351377
|
C | T | 1 | a0001c0002t0002g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.497-86231C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141351377 | ||||||
| chr7:141352068
|
G | A | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.497-85540G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141352068 | ||||||
| chr7:141352118
|
G | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.497-85490G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141352118 | ||||||
| chr7:141352353
|
G | A | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.497-85255G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141352353 | ||||||
| chr7:141352377
|
AT | A | 28 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(25): Show | 28 | HG00544.hp1 HG00544.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.497-85213delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141352377 | |||||
| chr7:141353068
|
A | C | 15 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(12): Show | 15 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.497-84540A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141353068 | ||||||
| chr7:141353719
|
A | G | 40 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0080others(37): Show | 40 | HG00544.hp1 HG00544.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.497-83889A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141353719 | ||||||
| chr7:141353745
|
G | A | 17 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(14): Show | 17 | HG00544.hp1 HG00544.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.497-83863G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141353745 | ||||||
| chr7:141353996
|
A | G | 2 | a0001c0001t0005g0008a0001c0001t0044g0001 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.497-83612A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141353996 | ||||||
| chr7:141354098
|
C | T | 1 | a0001c0002t0011g0044 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.497-83510C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141354098 | ||||||
| chr7:141354175
|
C | T | 5 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-83433C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141354175 | ||||||
| chr7:141354326
|
G | A | 1 | a0001c0002t0002g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.497-83282G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141354326 | ||||||
| chr7:141354451
|
G | GT | 15 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(12): Show | 15 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.497-83155dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141354451 | |||||
| chr7:141354472
|
A | G | 32 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(29): Show | 32 | HG00544.hp1 HG00544.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.497-83136A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141354472 | ||||||
| chr7:141354484
|
C | G | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.497-83124C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141354484 | ||||||
| chr7:141354521
|
G | A | 7 | a0001c0001t0005g0008a0001c0001t0008g0004a0001c0001t0009g0078others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.497-83087G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141354521 | ||||||
| chr7:141354859
|
C | G | 1 | a0001c0002t0013g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.497-82749C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141354859 | ||||||
| chr7:141355381
|
T | C | 32 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(29): Show | 32 | HG00544.hp1 HG00544.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.497-82227T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141355381 | ||||||
| chr7:141355847
|
A | G | 10 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(7): Show | 10 | HG00544.hp1 HG00544.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-81761A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141355847 | ||||||
| chr7:141355877
|
C | T | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-81731C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141355877 | ||||||
| chr7:141356016
|
C | T | 1 | a0001c0003t0001g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.497-81592C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141356016 | ||||||
| chr7:141356107
|
T | C | 5 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-81501T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141356107 | ||||||
| chr7:141356181
|
CA | C | 3 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.497-81424delA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141356181 | |||||
| chr7:141356186
|
G | C | 8 | a0001c0001t0001g0015a0001c0001t0004g0029a0001c0001t0006g0017others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.497-81422G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141356186 | ||||||
| chr7:141356380
|
G | GT | 32 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(29): Show | 32 | HG00544.hp1 HG00544.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.497-81218dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141356380 | |||||
| chr7:141356455
|
A | G | 32 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(29): Show | 32 | HG00544.hp1 HG00544.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.497-81153A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141356455 | ||||||
| chr7:141356549
|
C | T | 32 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(29): Show | 32 | HG00544.hp1 HG00544.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.497-81059C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141356549 | ||||||
| chr7:141356641
|
C | T | 5 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-80967C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141356641 | ||||||
| chr7:141356844
|
T | G | 1 | a0001c0001t0035g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.497-80764T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141356844 | ||||||
| chr7:141356990
|
T | C | 15 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(12): Show | 15 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.497-80618T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141356990 | ||||||
| chr7:141358252
|
A | G | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-79356A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141358252 | ||||||
| chr7:141358302
|
C | T | 1 | a0001c0001t0022g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.497-79306C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141358302 | ||||||
| chr7:141358598
|
C | G | 2 | a0001c0001t0005g0008a0001c0001t0044g0001 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.497-79010C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141358598 | ||||||
| chr7:141358722
|
G | A | 2 | a0001c0001t0006g0017a0001c0001t0011g0016 | 2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.497-78886G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141358722 | ||||||
| chr7:141359245
|
A | T | 1 | a0001c0001t0001g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.497-78363A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141359245 | ||||||
| chr7:141359410
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0004g0029a0001c0001t0006g0017others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.497-78198C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141359410 | ||||||
| chr7:141359673
|
G | T | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.497-77935G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141359673 | ||||||
| chr7:141359738
|
T | G | 40 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0080others(37): Show | 40 | HG00544.hp1 HG00544.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.497-77870T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141359738 | ||||||
| chr7:141359999
|
C | T | 1 | a0001c0002t0007g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.497-77609C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141359999 | ||||||
| chr7:141360000
|
G | A | 3 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.497-77608G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141360000 | ||||||
| chr7:141361218
|
T | C | 1 | a0001c0001t0034g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.497-76390T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141361218 | ||||||
| chr7:141361248
|
A | G | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.497-76360A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141361248 | ||||||
| chr7:141361361
|
T | TA | 5 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-76237dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141361361 | |||||
| chr7:141361417
|
T | G | 1 | a0001c0003t0001g0068 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.497-76191T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141361417 | ||||||
| chr7:141361495
|
A | G | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.497-76113A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141361495 | ||||||
| chr7:141361761
|
A | G | 3 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.497-75847A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141361761 | ||||||
| chr7:141362504
|
CT | C | 7 | a0001c0001t0004g0029a0001c0001t0006g0017a0001c0001t0011g0016others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.497-75094delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141362504 | |||||
| chr7:141362514
|
T | A | 2 | a0001c0001t0023g0018a0001c0002t0001g0048 | 2 | HG01952.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.497-75094T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141362514 | ||||||
| chr7:141362639
|
G | C | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.497-74969G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141362639 | ||||||
| chr7:141362825
|
C | G | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.497-74783C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141362825 | ||||||
| chr7:141362871
|
T | A | 3 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.497-74737T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141362871 | ||||||
| chr7:141362938
|
A | C | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.497-74670A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141362938 | ||||||
| chr7:141363076
|
G | A | 5 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-74532G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141363076 | ||||||
| chr7:141363222
|
G | A | 3 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.497-74386G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141363222 | ||||||
| chr7:141363375
|
G | A | 5 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-74233G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141363375 | ||||||
| chr7:141363522
|
G | T | 4 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0001t0044g0001others(1): Show | 4 | HG02922.hp2 HG03453.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-74086G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141363522 | ||||||
| chr7:141363559
|
C | A | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-74049C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141363559 | ||||||
| chr7:141364025
|
T | G | 29 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(26): Show | 29 | HG00544.hp1 HG00544.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.497-73583T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141364025 | ||||||
| chr7:141364143
|
A | G | 3 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.497-73465A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141364143 | ||||||
| chr7:141364160
|
C | T | 3 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0001t0044g0001 | 3 | HG02922.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.497-73448C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141364160 | ||||||
| chr7:141364281
|
G | A | 39 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(36): Show | 39 | HG00544.hp1 HG00544.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.497-73327G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141364281 | ||||||
| chr7:141364631
|
G | T | 2 | a0001c0001t0006g0017a0001c0001t0011g0016 | 2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.497-72977G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141364631 | ||||||
| chr7:141364659
|
C | CA | 4 | a0001c0001t0006g0017a0001c0001t0015g0028a0001c0001t0035g0079others(1): Show | 4 | HG01255.hp1 HG02258.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-72923dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141364659 | |||||
| chr7:141364659
|
C | CAA | 11 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(8): Show | 11 | HG00544.hp1 HG00544.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.497-72924_497-7292 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141364659 | |||||
| chr7:141364659
|
CA | C | 13 | a0001c0001t0001g0015a0001c0001t0003g0007a0001c0001t0004g0029others(10): Show | 13 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.497-72923delA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141364659 | |||||
| chr7:141364659
|
CAA | C | 14 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0008g0030others(11): Show | 14 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-72924_497-7292 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141364659 | |||||
| chr7:141364740
|
C | T | 3 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.497-72868C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141364740 | ||||||
| chr7:141364893
|
T | TGA | 14 | a0001c0001t0004g0023a0001c0001t0008g0004a0001c0001t0008g0030others(11): Show | 14 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-72712_497-7271 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141364893 | |||||
| chr7:141364995
|
A | G | 14 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(11): Show | 14 | HG00544.hp1 HG00544.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.497-72613A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141364995 | ||||||
| chr7:141365142
|
T | C | 28 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(25): Show | 28 | HG00544.hp1 HG00544.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.497-72466T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141365142 | ||||||
| chr7:141365352
|
T | C | 1 | a0001c0002t0002g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.497-72256T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141365352 | ||||||
| chr7:141365374
|
T | G | 3 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016 | 3 | HG02258.hp2 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.497-72234T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141365374 | ||||||
| chr7:141365388
|
G | T | 1 | a0001c0002t0041g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.497-72220G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141365388 | ||||||
| chr7:141365867
|
G | A | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-71741G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141365867 | ||||||
| chr7:141365885
|
A | G | 5 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-71723A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141365885 | ||||||
| chr7:141366040
|
C | T | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-71568C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141366040 | ||||||
| chr7:141366259
|
T | C | 5 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-71349T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141366259 | ||||||
| chr7:141366450
|
A | T | 1 | a0001c0002t0001g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.497-71158A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141366450 | ||||||
| chr7:141366554
|
T | C | 29 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(26): Show | 29 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.497-71054T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141366554 | ||||||
| chr7:141366608
|
T | C | 26 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0023others(23): Show | 26 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.497-71000T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141366608 | ||||||
| chr7:141366635
|
T | C | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-70973T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141366635 | ||||||
| chr7:141366743
|
C | G | 1 | a0001c0002t0013g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.497-70865C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141366743 | ||||||
| chr7:141366854
|
C | T | 4 | a0001c0001t0001g0080a0001c0002t0013g0047a0001c0002t0032g0071others(1): Show | 4 | HG00544.hp1 HG00544.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-70754C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141366854 | ||||||
| chr7:141366963
|
A | C | 2 | a0001c0001t0005g0014a0001c0002t0024g0002 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.497-70645A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141366963 | ||||||
| chr7:141367030
|
C | T | 29 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(26): Show | 29 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.497-70578C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141367030 | ||||||
| chr7:141367063
|
CA | C | 3 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0025g0010 | 3 | HG02486.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.497-70544delA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141367063 | ||||||
| chr7:141367064
|
A | G | 11 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(8): Show | 11 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-70544A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141367064 | ||||||
| chr7:141367070
|
A | G | 14 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0023others(11): Show | 14 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-70538A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141367070 | ||||||
| chr7:141367084
|
A | T | 3 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0001t0044g0001 | 3 | HG02922.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.497-70524A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141367084 | ||||||
| chr7:141367085
|
G | T | 11 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(8): Show | 11 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-70523G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141367085 | ||||||
| chr7:141367086
|
G | T | 3 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.497-70522G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141367086 | ||||||
| chr7:141367095
|
G | T | 1 | a0001c0002t0002g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.497-70513G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141367095 | ||||||
| chr7:141367104
|
G | C | 11 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(8): Show | 11 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-70504G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141367104 | ||||||
| chr7:141367472
|
G | A | 4 | a0001c0001t0014g0033a0001c0001t0014g0039a0001c0001t0028g0022others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-70136G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141367472 | ||||||
| chr7:141368056
|
C | T | 3 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.497-69552C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141368056 | ||||||
| chr7:141368280
|
C | G | 8 | a0001c0001t0004g0029a0001c0001t0005g0008a0001c0001t0023g0018others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.497-69328C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141368280 | ||||||
| chr7:141368437
|
A | G | 3 | a0001c0001t0016g0037a0001c0002t0016g0072a0002c0006t0039g0061 | 3 | HG01261.hp2 HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.497-69171A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141368437 | ||||||
| chr7:141368619
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0006g0017a0001c0001t0011g0016 | 3 | HG02258.hp2 HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.497-68989G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141368619 | ||||||
| chr7:141369183
|
A | C | 8 | a0001c0001t0008g0030a0001c0001t0034g0009a0001c0002t0013g0059others(5): Show | 8 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.497-68425A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141369183 | ||||||
| chr7:141369310
|
C | T | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.497-68298C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141369310 | ||||||
| chr7:141369316
|
C | CGT | 4 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0012g0045others(1): Show | 4 | HG02083.hp2 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-68251_497-6825 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141369316 | |||||
| chr7:141369316
|
C | T | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-68292C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141369316 | ||||||
| chr7:141369316
|
CGT | C | 18 | a0001c0001t0004g0023a0001c0001t0004g0029a0001c0001t0005g0014others(15): Show | 18 | HG01255.hp2 HG01256.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.497-68251_497-6825 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141369316 | |||||
| chr7:141369316
|
CGTGT | C | 24 | a0001c0001t0001g0012a0001c0001t0002g0027a0001c0001t0004g0024others(21): Show | 24 | HG01106.hp2 HG01243.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.497-68253_497-6825 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141369316 | |||||
| chr7:141369316
|
CGTGTGT | C | 6 | a0001c0001t0011g0016a0001c0002t0001g0064a0001c0002t0002g0043others(3): Show | 6 | HG02027.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-68255_497-6825 others(10): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141369316 | |||||
| chr7:141369316
|
CGTGTGTG others(9): Show |
C | 1 | a0001c0001t0014g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.497-68265_497-6825 others(20): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141369316 | |||||
| chr7:141369347
|
GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.497-68249_497-6823 others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141369347 | |||||
| chr7:141369349
|
GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0001g0035 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.497-68249_497-6824 others(14): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141369349 | |||||
| chr7:141369353
|
G | A | 12 | a0001c0001t0004g0023a0001c0001t0008g0030a0001c0001t0010g0021others(9): Show | 12 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.497-68255G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141369353 | ||||||
| chr7:141369357
|
GTA | G | 2 | a0001c0002t0013g0047a0001c0005t0001g0005 | 2 | HG00544.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.497-68249_497-6824 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141369357 | |||||
| chr7:141369359
|
A | G | 2 | a0001c0001t0001g0080a0001c0002t0032g0071 | 2 | HG00544.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.497-68249A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141369359 | ||||||
| chr7:141369547
|
G | A | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.497-68061G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141369547 | ||||||
| chr7:141369863
|
A | G | 21 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(18): Show | 21 | HG00544.hp1 HG00544.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.497-67745A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141369863 | ||||||
| chr7:141369943
|
A | C | 24 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(21): Show | 24 | HG00544.hp1 HG00544.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.497-67665A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141369943 | ||||||
| chr7:141370100
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0011g0016others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-67508C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141370100 | ||||||
| chr7:141370116
|
AGT | A | 39 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(36): Show | 39 | HG00544.hp1 HG00544.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.497-67484_497-6748 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141370116 | |||||
| chr7:141370160
|
G | T | 3 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.497-67448G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141370160 | ||||||
| chr7:141370278
|
G | A | 5 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-67330G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141370278 | ||||||
| chr7:141370393
|
A | G | 4 | a0001c0001t0001g0080a0001c0002t0013g0047a0001c0002t0032g0071others(1): Show | 4 | HG00544.hp1 HG00544.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-67215A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141370393 | ||||||
| chr7:141370418
|
G | A | 73 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(70): Show | 73 | HG00544.hp1 HG00544.hp2 HG01106.hp2 others(70): Show |
intron_variant | MODIFIER | c.497-67190G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141370418 | ||||||
| chr7:141370524
|
G | A | 20 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0023others(17): Show | 20 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.497-67084G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141370524 | ||||||
| chr7:141370600
|
T | TG | 46 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0080others(43): Show | 46 | HG00544.hp1 HG00544.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.497-67006dupG | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141370600 | |||||
| chr7:141370764
|
G | A | 7 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0008g0004others(4): Show | 7 | HG02486.hp1 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.497-66844G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141370764 | ||||||
| chr7:141370828
|
G | A | 3 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0001t0044g0001 | 3 | HG02922.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.497-66780G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141370828 | ||||||
| chr7:141371172
|
A | G | 8 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(5): Show | 8 | HG00544.hp1 HG00544.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.497-66436A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141371172 | ||||||
| chr7:141371296
|
T | TA | 9 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(6): Show | 9 | HG00544.hp1 HG00544.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-66302dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141371296 | |||||
| chr7:141371417
|
G | A | 5 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-66191G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141371417 | ||||||
| chr7:141371547
|
C | A | 3 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.497-66061C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141371547 | ||||||
| chr7:141371896
|
G | T | 33 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(30): Show | 33 | HG00544.hp1 HG00544.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.497-65712G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141371896 | ||||||
| chr7:141371995
|
C | T | 1 | a0001c0002t0001g0064 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.497-65613C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141371995 | ||||||
| chr7:141372333
|
C | T | 3 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0001t0044g0001 | 3 | HG02922.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.497-65275C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141372333 | ||||||
| chr7:141372334
|
A | G | 39 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(36): Show | 39 | HG00544.hp1 HG00544.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.497-65274A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141372334 | ||||||
| chr7:141372460
|
T | C | 1 | a0001c0001t0011g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.497-65148T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141372460 | ||||||
| chr7:141372900
|
C | T | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-64708C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141372900 | ||||||
| chr7:141373322
|
A | AAACAACA others(12): Show |
1 | a0001c0002t0001g0064 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.497-64272_497-6425 others(23): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141373322 | |||||
| chr7:141373328
|
C | A | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.497-64280C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141373328 | ||||||
| chr7:141373527
|
G | A | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-64081G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141373527 | ||||||
| chr7:141373718
|
C | G | 3 | a0001c0001t0008g0004a0001c0001t0009g0078a0001c0002t0026g0041 | 3 | HG02572.hp1 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.497-63890C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141373718 | ||||||
| chr7:141373798
|
C | T | 29 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0023others(26): Show | 29 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.497-63810C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141373798 | ||||||
| chr7:141373957
|
T | G | 17 | a0001c0001t0004g0023a0001c0001t0005g0008a0001c0001t0008g0030others(14): Show | 17 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.497-63651T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141373957 | ||||||
| chr7:141374234
|
C | T | 5 | a0001c0001t0004g0029a0001c0001t0033g0031a0001c0002t0003g0052others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-63374C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141374234 | ||||||
| chr7:141374239
|
T | C | 22 | a0001c0001t0004g0023a0001c0001t0004g0029a0001c0001t0005g0008others(19): Show | 22 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.497-63369T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141374239 | ||||||
| chr7:141374457
|
T | C | 8 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(5): Show | 8 | HG00544.hp1 HG00544.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.497-63151T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141374457 | ||||||
| chr7:141374585
|
C | T | 1 | a0001c0002t0042g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.497-63023C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141374585 | ||||||
| chr7:141374596
|
C | T | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.497-63012C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141374596 | ||||||
| chr7:141374852
|
G | A | 80 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(77): Show | 80 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.497-62756G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141374852 | ||||||
| chr7:141374917
|
G | A | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.497-62691G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141374917 | ||||||
| chr7:141375226
|
T | C | 12 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(9): Show | 12 | HG00544.hp1 HG00544.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.497-62382T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141375226 | ||||||
| chr7:141375257
|
A | G | 1 | a0001c0002t0011g0044 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.497-62351A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141375257 | ||||||
| chr7:141375399
|
G | A | 39 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(36): Show | 39 | HG00544.hp1 HG00544.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.497-62209G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141375399 | ||||||
| chr7:141376032
|
C | T | 1 | a0001c0002t0007g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.497-61576C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141376032 | ||||||
| chr7:141376229
|
T | G | 11 | a0001c0001t0002g0027a0001c0001t0008g0030a0001c0001t0035g0079others(8): Show | 11 | HG01243.hp2 HG01978.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.497-61379T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141376229 | ||||||
| chr7:141376565
|
A | G | 1 | a0001c0002t0009g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.497-61043A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141376565 | ||||||
| chr7:141376845
|
A | T | 20 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0005g0008others(17): Show | 20 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.497-60763A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141376845 | ||||||
| chr7:141377042
|
T | G | 6 | a0001c0001t0005g0008a0001c0001t0011g0016a0001c0001t0023g0018others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-60566T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141377042 | ||||||
| chr7:141377155
|
T | C | 5 | a0001c0001t0004g0029a0001c0001t0008g0004a0001c0001t0009g0078others(2): Show | 5 | HG02572.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.497-60453T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141377155 | ||||||
| chr7:141377159
|
G | GTATT | 22 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0004g0023others(19): Show | 22 | HG01243.hp2 HG01255.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.497-60411_497-6040 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141377159 | |||||
| chr7:141377159
|
G | GTATTTAT others(1): Show |
7 | a0001c0001t0001g0080a0001c0001t0002g0027a0001c0001t0022g0013others(4): Show | 7 | HG00544.hp1 HG00544.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.497-60415_497-6040 others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141377159 | |||||
| chr7:141377159
|
G | GTATTTAT others(5): Show |
1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.497-60419_497-6040 others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141377159 | |||||
| chr7:141377159
|
GTATTTAT others(1): Show |
G | 10 | a0001c0001t0004g0029a0001c0001t0008g0004a0001c0001t0009g0078others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-60415_497-6040 others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141377159 | |||||
| chr7:141377213
|
C | T | 1 | a0001c0002t0015g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.497-60395C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141377213 | ||||||
| chr7:141377372
|
C | T | 2 | a0001c0001t0016g0037a0001c0002t0016g0072 | 2 | HG01261.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.497-60236C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141377372 | ||||||
| chr7:141377555
|
C | T | 1 | a0001c0002t0001g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.497-60053C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141377555 | ||||||
| chr7:141377867
|
C | A | 4 | a0001c0001t0014g0033a0001c0001t0014g0039a0001c0001t0028g0022others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-59741C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141377867 | ||||||
| chr7:141377897
|
A | G | 8 | a0001c0001t0004g0029a0001c0001t0008g0004a0001c0001t0009g0078others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.497-59711A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141377897 | ||||||
| chr7:141377932
|
A | T | 2 | a0001c0002t0010g0066a0001c0002t0027g0051 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.497-59676A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141377932 | ||||||
| chr7:141378313
|
C | T | 8 | a0001c0001t0004g0029a0001c0001t0008g0004a0001c0001t0009g0078others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.497-59295C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141378313 | ||||||
| chr7:141378571
|
C | G | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.497-59037C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141378571 | ||||||
| chr7:141378584
|
T | C | 34 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0004g0029others(31): Show | 34 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.497-59024T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141378584 | ||||||
| chr7:141378944
|
A | G | 1 | a0001c0001t0035g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.497-58664A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141378944 | ||||||
| chr7:141379052
|
G | A | 8 | a0001c0001t0004g0029a0001c0001t0008g0004a0001c0001t0009g0078others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.497-58556G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141379052 | ||||||
| chr7:141379080
|
T | G | 11 | a0001c0001t0002g0027a0001c0001t0008g0030a0001c0001t0035g0079others(8): Show | 11 | HG01243.hp2 HG01978.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.497-58528T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141379080 | ||||||
| chr7:141379304
|
T | TA | 8 | a0001c0001t0004g0023a0001c0001t0010g0021a0001c0001t0034g0009others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.497-58288dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141379304 | |||||
| chr7:141379304
|
T | TAA | 9 | a0001c0001t0004g0029a0001c0001t0008g0004a0001c0001t0009g0078others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-58289_497-5828 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141379304 | |||||
| chr7:141379304
|
TA | T | 4 | a0001c0001t0003g0007a0001c0001t0011g0016a0001c0002t0001g0042others(1): Show | 4 | HG02572.hp2 HG02897.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-58288delA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141379304 | |||||
| chr7:141379317
|
A | AAAG | 10 | a0001c0001t0002g0027a0001c0001t0008g0030a0001c0001t0035g0079others(7): Show | 10 | HG01243.hp2 HG01978.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.497-58289_497-5828 others(7): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141379317 | |||||
| chr7:141379432
|
C | G | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-58176C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141379432 | ||||||
| chr7:141379473
|
A | AATCC | 11 | a0001c0001t0002g0027a0001c0001t0008g0030a0001c0001t0035g0079others(8): Show | 11 | HG01243.hp2 HG01978.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.497-58134_497-5813 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141379473 | |||||
| chr7:141379573
|
G | A | 1 | a0001c0001t0006g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.497-58035G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141379573 | ||||||
| chr7:141380116
|
C | T | 1 | a0001c0001t0006g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.497-57492C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141380116 | ||||||
| chr7:141380180
|
G | A | 1 | a0001c0001t0011g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.497-57428G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141380180 | ||||||
| chr7:141380281
|
A | AAATCT | 3 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0001t0044g0001 | 3 | HG02922.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.497-57321_497-5731 others(9): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141380281 | |||||
| chr7:141380526
|
G | A | 11 | a0001c0001t0002g0027a0001c0001t0008g0030a0001c0001t0035g0079others(8): Show | 11 | HG01243.hp2 HG01978.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.497-57082G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141380526 | ||||||
| chr7:141380538
|
C | T | 11 | a0001c0001t0002g0027a0001c0001t0008g0030a0001c0001t0035g0079others(8): Show | 11 | HG01243.hp2 HG01978.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.497-57070C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141380538 | ||||||
| chr7:141380577
|
T | G | 13 | a0001c0001t0002g0027a0001c0001t0008g0030a0001c0001t0011g0016others(10): Show | 13 | HG01243.hp2 HG01978.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.497-57031T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141380577 | ||||||
| chr7:141380653
|
A | G | 9 | a0001c0001t0004g0024a0001c0001t0005g0014a0001c0001t0015g0028others(6): Show | 9 | HG01261.hp2 HG01891.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.497-56955A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141380653 | ||||||
| chr7:141380665
|
G | A | 1 | a0001c0002t0012g0045 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.497-56943G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141380665 | ||||||
| chr7:141380665
|
G | C | 10 | a0001c0001t0002g0027a0001c0001t0008g0030a0001c0001t0035g0079others(7): Show | 10 | HG01243.hp2 HG01978.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.497-56943G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141380665 | ||||||
| chr7:141381150
|
C | T | 2 | a0001c0001t0005g0008a0001c0001t0023g0018 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-56458C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141381150 | ||||||
| chr7:141381648
|
A | G | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.497-55960A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141381648 | ||||||
| chr7:141381725
|
C | T | 10 | a0001c0001t0002g0027a0001c0001t0008g0030a0001c0001t0035g0079others(7): Show | 10 | HG01243.hp2 HG01978.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.497-55883C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141381725 | ||||||
| chr7:141381867
|
A | G | 4 | a0001c0002t0001g0057a0001c0002t0001g0064a0001c0002t0007g0053others(1): Show | 4 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-55741A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141381867 | ||||||
| chr7:141381952
|
G | T | 30 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0004g0029others(27): Show | 30 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.497-55656G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141381952 | ||||||
| chr7:141382002
|
T | C | 11 | a0001c0001t0004g0023a0001c0001t0010g0021a0001c0001t0011g0016others(8): Show | 11 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-55606T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141382002 | ||||||
| chr7:141382028
|
C | T | 1 | a0001c0002t0007g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.497-55580C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141382028 | ||||||
| chr7:141382126
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.497-55482C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141382126 | ||||||
| chr7:141382224
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.497-55384G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141382224 | ||||||
| chr7:141382293
|
C | T | 3 | a0001c0002t0003g0052a0001c0002t0015g0056a0001c0002t0030g0067 | 3 | HG01891.hp2 HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.497-55315C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141382293 | ||||||
| chr7:141382743
|
A | T | 9 | a0001c0001t0004g0023a0001c0001t0010g0021a0001c0001t0034g0009others(6): Show | 9 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-54865A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141382743 | ||||||
| chr7:141382760
|
T | C | 2 | a0001c0001t0011g0016a0001c0001t0025g0010 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.497-54848T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141382760 | ||||||
| chr7:141382911
|
G | A | 1 | a0001c0001t0011g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.497-54697G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141382911 | ||||||
| chr7:141383038
|
T | C | 9 | a0001c0001t0004g0023a0001c0001t0010g0021a0001c0001t0034g0009others(6): Show | 9 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-54570T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141383038 | ||||||
| chr7:141383144
|
TTTTC | T | 7 | a0001c0001t0004g0029a0001c0001t0008g0004a0001c0001t0009g0078others(4): Show | 7 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.497-54444_497-5444 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141383144 | |||||
| chr7:141383159
|
TCTTTC | T | 2 | a0001c0001t0011g0016a0001c0002t0030g0067 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.497-54448_497-5444 others(9): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141383159 | ||||||
| chr7:141383162
|
TTC | T | 10 | a0001c0001t0002g0027a0001c0001t0008g0030a0001c0001t0035g0079others(7): Show | 10 | HG01243.hp2 HG01978.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.497-54444_497-5444 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141383162 | |||||
| chr7:141383164
|
C | T | 8 | a0001c0001t0004g0029a0001c0001t0008g0004a0001c0001t0009g0078others(5): Show | 8 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.497-54444C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141383164 | ||||||
| chr7:141383174
|
A | T | 10 | a0001c0001t0002g0027a0001c0001t0008g0030a0001c0001t0035g0079others(7): Show | 10 | HG01243.hp2 HG01978.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.497-54434A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141383174 | ||||||
| chr7:141383215
|
AATTCTTT others(4): Show |
A | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-54392_497-5438 others(15): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141383215 | ||||||
| chr7:141383229
|
T | A | 10 | a0001c0001t0002g0027a0001c0001t0008g0030a0001c0001t0035g0079others(7): Show | 10 | HG01243.hp2 HG01978.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.497-54379T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141383229 | ||||||
| chr7:141383295
|
T | G | 4 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0001t0044g0001others(1): Show | 4 | HG02922.hp2 HG03453.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-54313T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141383295 | ||||||
| chr7:141383317
|
C | T | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-54291C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141383317 | ||||||
| chr7:141383318
|
A | G | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-54290A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141383318 | ||||||
| chr7:141383321
|
A | C | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-54287A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141383321 | ||||||
| chr7:141383325
|
C | T | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-54283C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141383325 | ||||||
| chr7:141383342
|
G | A | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-54266G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141383342 | ||||||
| chr7:141383344
|
G | A | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-54264G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141383344 | ||||||
| chr7:141383367
|
C | G | 1 | a0001c0001t0012g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.497-54241C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141383367 | ||||||
| chr7:141383594
|
A | G | 22 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(19): Show | 22 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.497-54014A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141383594 | ||||||
| chr7:141383817
|
A | G | 1 | a0001c0002t0007g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.497-53791A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141383817 | ||||||
| chr7:141383984
|
C | T | 36 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(33): Show | 36 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.497-53624C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141383984 | ||||||
| chr7:141384291
|
C | A | 2 | a0001c0001t0011g0016a0001c0001t0025g0010 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.497-53317C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141384291 | ||||||
| chr7:141384373
|
T | C | 10 | a0001c0001t0002g0027a0001c0001t0008g0030a0001c0001t0035g0079others(7): Show | 10 | HG01243.hp2 HG01978.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.497-53235T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141384373 | ||||||
| chr7:141384558
|
C | G | 1 | a0001c0002t0001g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.497-53050C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141384558 | ||||||
| chr7:141384562
|
T | C | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-53046T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141384562 | ||||||
| chr7:141384739
|
T | C | 10 | a0001c0001t0002g0027a0001c0001t0008g0030a0001c0001t0035g0079others(7): Show | 10 | HG01243.hp2 HG01978.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.497-52869T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141384739 | ||||||
| chr7:141385169
|
G | A | 14 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(11): Show | 14 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-52439G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141385169 | ||||||
| chr7:141385189
|
G | C | 40 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0002g0019others(37): Show | 40 | HG00544.hp1 HG00544.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.497-52419G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141385189 | ||||||
| chr7:141385225
|
A | G | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-52383A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141385225 | ||||||
| chr7:141385399
|
C | T | 2 | a0001c0001t0011g0016a0001c0001t0025g0010 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.497-52209C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141385399 | ||||||
| chr7:141385630
|
G | A | 3 | a0001c0001t0003g0020a0001c0001t0005g0014a0001c0002t0009g0060 | 3 | HG03139.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.497-51978G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141385630 | ||||||
| chr7:141385714
|
A | G | 34 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0004g0029others(31): Show | 34 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.497-51894A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141385714 | ||||||
| chr7:141385854
|
T | C | 34 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0004g0029others(31): Show | 34 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.497-51754T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141385854 | ||||||
| chr7:141386537
|
C | T | 9 | a0001c0001t0004g0029a0001c0001t0008g0004a0001c0001t0009g0078others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-51071C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141386537 | ||||||
| chr7:141386721
|
C | T | 3 | a0001c0002t0003g0052a0001c0002t0015g0056a0001c0002t0030g0067 | 3 | HG01891.hp2 HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.497-50887C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141386721 | ||||||
| chr7:141386722
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.497-50886G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141386722 | ||||||
| chr7:141386727
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.497-50881C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141386727 | ||||||
| chr7:141386732
|
G | T | 8 | a0001c0001t0004g0029a0001c0001t0008g0004a0001c0001t0009g0078others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.497-50876G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141386732 | ||||||
| chr7:141386899
|
T | C | 16 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(13): Show | 16 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.497-50709T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141386899 | ||||||
| chr7:141387890
|
T | G | 2 | a0001c0001t0011g0016a0001c0001t0025g0010 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.497-49718T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141387890 | ||||||
| chr7:141387893
|
C | T | 3 | a0001c0002t0003g0052a0001c0002t0015g0056a0001c0002t0030g0067 | 3 | HG01891.hp2 HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.497-49715C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141387893 | ||||||
| chr7:141388003
|
G | A | 5 | a0001c0001t0038g0034a0001c0002t0001g0057a0001c0002t0001g0064others(2): Show | 5 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.497-49605G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141388003 | ||||||
| chr7:141388016
|
G | C | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-49592G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141388016 | ||||||
| chr7:141388359
|
C | T | 1 | a0001c0003t0019g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497-49249C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141388359 | ||||||
| chr7:141388375
|
C | T | 1 | a0002c0006t0039g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.497-49233C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141388375 | ||||||
| chr7:141388676
|
ACC | A | 3 | a0001c0002t0003g0052a0001c0002t0015g0056a0001c0002t0030g0067 | 3 | HG01891.hp2 HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.497-48931_497-4893 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141388676 | ||||||
| chr7:141388698
|
G | A | 14 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(11): Show | 14 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-48910G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141388698 | ||||||
| chr7:141388702
|
G | A | 3 | a0001c0002t0003g0052a0001c0002t0015g0056a0001c0002t0030g0067 | 3 | HG01891.hp2 HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.497-48906G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141388702 | ||||||
| chr7:141388745
|
A | G | 25 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(22): Show | 25 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.497-48863A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141388745 | ||||||
| chr7:141388779
|
CT | C | 2 | a0001c0001t0001g0035a0001c0001t0002g0019 | 2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.497-48828delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141388779 | ||||||
| chr7:141388788
|
A | G | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-48820A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141388788 | ||||||
| chr7:141388805
|
A | G | 2 | a0001c0001t0011g0016a0001c0001t0025g0010 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.497-48803A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141388805 | ||||||
| chr7:141388857
|
A | C | 16 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(13): Show | 16 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.497-48751A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141388857 | ||||||
| chr7:141388898
|
C | CGGATGTT others(3): Show |
14 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(11): Show | 14 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-48710_497-4870 others(14): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141388898 | ||||||
| chr7:141388902
|
G | A | 14 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(11): Show | 14 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-48706G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141388902 | ||||||
| chr7:141388903
|
T | A | 14 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(11): Show | 14 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-48705T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141388903 | ||||||
| chr7:141388927
|
C | T | 14 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(11): Show | 14 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-48681C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141388927 | ||||||
| chr7:141389170
|
A | G | 80 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(77): Show | 80 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.497-48438A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141389170 | ||||||
| chr7:141389186
|
G | A | 14 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(11): Show | 14 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-48422G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141389186 | ||||||
| chr7:141389363
|
T | C | 31 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(28): Show | 31 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.497-48245T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141389363 | ||||||
| chr7:141389475
|
A | G | 3 | a0001c0002t0003g0052a0001c0002t0015g0056a0001c0002t0030g0067 | 3 | HG01891.hp2 HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.497-48133A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141389475 | ||||||
| chr7:141389555
|
A | G | 1 | a0001c0001t0004g0023 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.497-48053A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141389555 | ||||||
| chr7:141389649
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.497-47959G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141389649 | ||||||
| chr7:141389704
|
A | G | 1 | a0001c0001t0002g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.497-47904A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141389704 | ||||||
| chr7:141389844
|
C | T | 14 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(11): Show | 14 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-47764C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141389844 | ||||||
| chr7:141389955
|
T | C | 14 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(11): Show | 14 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-47653T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141389955 | ||||||
| chr7:141389996
|
G | A | 1 | a0001c0002t0006g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.497-47612G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141389996 | ||||||
| chr7:141390063
|
A | G | 4 | a0001c0001t0015g0028a0001c0001t0021g0077a0001c0002t0005g0049others(1): Show | 4 | HG03471.hp2 HG03516.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-47545A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141390063 | ||||||
| chr7:141390123
|
GAGAA | G | 13 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(10): Show | 13 | HG01255.hp2 HG01884.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.497-47477_497-4747 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141390123 | |||||
| chr7:141390127
|
A | G | 1 | a0001c0002t0036g0069 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.497-47481A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141390127 | ||||||
| chr7:141390306
|
C | T | 2 | a0001c0002t0040g0050a0001c0004t0043g0032 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.497-47302C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141390306 | ||||||
| chr7:141390368
|
A | C | 11 | a0001c0001t0011g0016a0001c0001t0025g0010a0001c0001t0038g0034others(8): Show | 11 | HG01243.hp2 HG01891.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-47240A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141390368 | ||||||
| chr7:141390567
|
G | A | 2 | a0001c0001t0025g0010a0001c0002t0007g0053 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.497-47041G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141390567 | ||||||
| chr7:141390606
|
G | A | 15 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(12): Show | 15 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.497-47002G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141390606 | ||||||
| chr7:141390765
|
A | T | 5 | a0001c0001t0038g0034a0001c0002t0001g0057a0001c0002t0001g0064others(2): Show | 5 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.497-46843A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141390765 | ||||||
| chr7:141391010
|
C | T | 19 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0005g0008others(16): Show | 19 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.497-46598C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141391010 | ||||||
| chr7:141391175
|
C | CT | 7 | a0001c0001t0011g0016a0001c0001t0025g0010a0001c0001t0038g0034others(4): Show | 7 | HG01243.hp2 HG01978.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.497-46424dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141391175 | |||||
| chr7:141391346
|
A | G | 2 | a0001c0001t0011g0016a0001c0001t0025g0010 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.497-46262A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141391346 | ||||||
| chr7:141391390
|
T | G | 15 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(12): Show | 15 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.497-46218T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141391390 | ||||||
| chr7:141391428
|
G | C | 2 | a0001c0001t0011g0016a0001c0001t0025g0010 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.497-46180G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141391428 | ||||||
| chr7:141391677
|
T | C | 30 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0005g0008others(27): Show | 30 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.497-45931T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141391677 | ||||||
| chr7:141391700
|
C | T | 3 | a0001c0002t0003g0052a0001c0002t0015g0056a0001c0002t0030g0067 | 3 | HG01891.hp2 HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.497-45908C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141391700 | ||||||
| chr7:141391943
|
A | G | 30 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0005g0008others(27): Show | 30 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.497-45665A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141391943 | ||||||
| chr7:141392061
|
G | GT | 28 | a0001c0001t0002g0027a0001c0001t0003g0007a0001c0001t0004g0023others(25): Show | 28 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.497-45536dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141392061 | |||||
| chr7:141392086
|
A | G | 22 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0005g0008others(19): Show | 22 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.497-45522A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141392086 | ||||||
| chr7:141392151
|
T | C | 2 | a0001c0001t0011g0016a0001c0001t0025g0010 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.497-45457T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141392151 | ||||||
| chr7:141392185
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.497-45423C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141392185 | ||||||
| chr7:141392391
|
C | G | 4 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0001t0044g0001others(1): Show | 4 | HG02922.hp2 HG03453.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-45217C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141392391 | ||||||
| chr7:141392719
|
T | C | 30 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0005g0008others(27): Show | 30 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.497-44889T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141392719 | ||||||
| chr7:141392813
|
A | T | 3 | a0001c0002t0003g0052a0001c0002t0015g0056a0001c0002t0030g0067 | 3 | HG01891.hp2 HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.497-44795A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141392813 | ||||||
| chr7:141393083
|
C | T | 16 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(13): Show | 16 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.497-44525C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141393083 | ||||||
| chr7:141393089
|
G | A | 1 | a0001c0001t0011g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.497-44519G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141393089 | ||||||
| chr7:141393559
|
C | T | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.497-44049C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141393559 | ||||||
| chr7:141393812
|
A | G | 20 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0005g0008others(17): Show | 20 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.497-43796A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141393812 | ||||||
| chr7:141394041
|
G | T | 16 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0008g0030others(13): Show | 16 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.497-43567G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141394041 | ||||||
| chr7:141394246
|
C | T | 3 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0002t0002g0043 | 3 | HG02922.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-43362C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141394246 | ||||||
| chr7:141394439
|
C | T | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-43169C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141394439 | ||||||
| chr7:141394500
|
A | G | 5 | a0001c0001t0038g0034a0001c0002t0001g0057a0001c0002t0001g0064others(2): Show | 5 | HG01243.hp2 HG01978.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.497-43108A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141394500 | ||||||
| chr7:141395313
|
T | C | 24 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0005g0008others(21): Show | 24 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.497-42295T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141395313 | ||||||
| chr7:141395345
|
G | T | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.497-42263G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141395345 | ||||||
| chr7:141395351
|
A | G | 26 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(23): Show | 26 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.497-42257A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141395351 | ||||||
| chr7:141395683
|
A | G | 26 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(23): Show | 26 | HG01243.hp2 HG01255.hp2 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.497-41925A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141395683 | ||||||
| chr7:141396064
|
G | A | 27 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0002g0019others(24): Show | 27 | HG01106.hp2 HG01243.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.497-41544G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141396064 | ||||||
| chr7:141396204
|
G | A | 1 | a0001c0002t0002g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.497-41404G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141396204 | ||||||
| chr7:141396247
|
G | A | 27 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0002g0019others(24): Show | 27 | HG01106.hp2 HG01243.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.497-41361G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141396247 | ||||||
| chr7:141396398
|
G | T | 2 | a0001c0002t0001g0048a0001c0002t0001g0065 | 2 | HG01952.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.497-41210G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141396398 | ||||||
| chr7:141396495
|
C | T | 1 | a0001c0001t0004g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.497-41113C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141396495 | ||||||
| chr7:141396529
|
CAG | C | 27 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0002g0019others(24): Show | 27 | HG01106.hp2 HG01243.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.497-41076_497-4107 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141396529 | |||||
| chr7:141396968
|
C | A | 1 | a0001c0003t0001g0068 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.497-40640C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141396968 | ||||||
| chr7:141397315
|
TC | T | 16 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(13): Show | 16 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.497-40291delC | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141397315 | |||||
| chr7:141397550
|
G | C | 2 | a0001c0001t0016g0037a0001c0002t0016g0072 | 2 | HG01261.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.497-40058G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141397550 | ||||||
| chr7:141397585
|
G | A | 16 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(13): Show | 16 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.497-40023G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141397585 | ||||||
| chr7:141397792
|
A | G | 8 | a0001c0001t0004g0024a0001c0001t0015g0028a0001c0001t0016g0037others(5): Show | 8 | HG01261.hp2 HG01891.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.497-39816A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141397792 | ||||||
| chr7:141398091
|
G | T | 4 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0011g0016others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-39517G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141398091 | ||||||
| chr7:141398624
|
G | A | 27 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0002g0019others(24): Show | 27 | HG01106.hp2 HG01243.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.497-38984G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141398624 | ||||||
| chr7:141398784
|
G | A | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-38824G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141398784 | ||||||
| chr7:141398838
|
A | G | 5 | a0001c0001t0001g0015a0001c0001t0014g0033a0001c0001t0014g0039others(2): Show | 5 | HG01243.hp1 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.497-38770A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141398838 | ||||||
| chr7:141399162
|
T | A | 4 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0011g0016others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-38446T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141399162 | ||||||
| chr7:141399341
|
C | T | 12 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0010g0021others(9): Show | 12 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.497-38267C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141399341 | ||||||
| chr7:141399384
|
G | T | 4 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0011g0016others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-38224G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141399384 | ||||||
| chr7:141399716
|
C | T | 1 | a0001c0002t0011g0044 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.497-37892C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141399716 | ||||||
| chr7:141399809
|
C | G | 4 | a0001c0001t0001g0080a0001c0002t0013g0047a0001c0002t0032g0071others(1): Show | 4 | HG00544.hp1 HG00544.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-37799C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141399809 | ||||||
| chr7:141400254
|
A | C | 4 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0001t0044g0001others(1): Show | 4 | HG02922.hp2 HG03453.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-37354A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141400254 | ||||||
| chr7:141400281
|
C | T | 5 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0001t0044g0001others(2): Show | 5 | HG02922.hp2 HG03453.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-37327C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141400281 | ||||||
| chr7:141400443
|
G | A | 3 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0002t0002g0043 | 3 | HG02922.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-37165G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141400443 | ||||||
| chr7:141400765
|
G | A | 1 | a0001c0002t0001g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.497-36843G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141400765 | ||||||
| chr7:141400882
|
T | C | 1 | a0001c0001t0011g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.497-36726T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141400882 | ||||||
| chr7:141401463
|
G | A | 1 | a0001c0001t0038g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.497-36145G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141401463 | ||||||
| chr7:141401581
|
A | AT | 4 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0011g0016others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-36020dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141401581 | |||||
| chr7:141401588
|
TA | T | 7 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0010g0021others(4): Show | 7 | HG01952.hp2 HG02258.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.497-36019delA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141401588 | ||||||
| chr7:141401589
|
A | T | 4 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0001t0044g0001others(1): Show | 4 | HG02922.hp2 HG03453.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-36019A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141401589 | ||||||
| chr7:141401618
|
C | T | 6 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0010g0021others(3): Show | 6 | HG01952.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-35990C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141401618 | ||||||
| chr7:141401671
|
G | A | 2 | a0001c0001t0003g0007a0001c0001t0029g0026 | 2 | HG01884.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.497-35937G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141401671 | ||||||
| chr7:141401684
|
G | A | 7 | a0001c0001t0003g0007a0001c0001t0012g0036a0001c0001t0029g0026others(4): Show | 7 | HG01884.hp2 HG01952.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.497-35924G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141401684 | ||||||
| chr7:141401696
|
G | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.497-35912G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141401696 | ||||||
| chr7:141402102
|
A | G | 14 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(11): Show | 14 | HG01952.hp2 HG02258.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-35506A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141402102 | ||||||
| chr7:141402140
|
C | A | 1 | a0001c0001t0011g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.497-35468C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141402140 | ||||||
| chr7:141402284
|
C | T | 4 | a0001c0001t0005g0008a0001c0001t0023g0018a0001c0001t0044g0001others(1): Show | 4 | HG02922.hp2 HG03453.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-35324C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141402284 | ||||||
| chr7:141402653
|
A | G | 5 | a0001c0001t0005g0008a0001c0001t0011g0016a0001c0001t0023g0018others(2): Show | 5 | HG02572.hp2 HG02922.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-34955A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141402653 | ||||||
| chr7:141402782
|
G | A | 1 | a0001c0001t0022g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.497-34826G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141402782 | ||||||
| chr7:141402924
|
C | T | 1 | a0001c0002t0001g0057 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.497-34684C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141402924 | ||||||
| chr7:141403213
|
C | T | 1 | a0001c0003t0019g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497-34395C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141403213 | ||||||
| chr7:141403400
|
A | G | 3 | a0001c0001t0004g0023a0001c0001t0010g0021a0001c0002t0042g0054 | 3 | HG01952.hp2 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.497-34208A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141403400 | ||||||
| chr7:141403405
|
T | C | 80 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(77): Show | 80 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.497-34203T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141403405 | ||||||
| chr7:141403606
|
T | C | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.497-34002T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141403606 | ||||||
| chr7:141403679
|
G | A | 2 | a0001c0001t0005g0008a0001c0001t0023g0018 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-33929G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141403679 | ||||||
| chr7:141403878
|
A | G | 2 | a0001c0001t0005g0008a0001c0001t0023g0018 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-33730A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141403878 | ||||||
| chr7:141404042
|
G | A | 2 | a0001c0001t0005g0008a0001c0001t0023g0018 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-33566G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141404042 | ||||||
| chr7:141404080
|
C | T | 1 | a0001c0001t0035g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.497-33528C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141404080 | ||||||
| chr7:141404094
|
A | G | 2 | a0001c0001t0005g0008a0001c0001t0023g0018 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-33514A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141404094 | ||||||
| chr7:141404129
|
C | T | 2 | a0001c0001t0005g0008a0001c0001t0023g0018 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-33479C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141404129 | ||||||
| chr7:141404174
|
A | G | 2 | a0001c0001t0005g0008a0001c0001t0023g0018 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-33434A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141404174 | ||||||
| chr7:141404247
|
A | G | 80 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(77): Show | 80 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.497-33361A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141404247 | ||||||
| chr7:141404264
|
T | C | 2 | a0001c0001t0005g0008a0001c0001t0023g0018 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-33344T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141404264 | ||||||
| chr7:141404585
|
A | G | 1 | a0001c0002t0017g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.497-33023A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141404585 | ||||||
| chr7:141404678
|
A | G | 1 | a0001c0001t0011g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.497-32930A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141404678 | ||||||
| chr7:141404768
|
A | T | 1 | a0001c0002t0042g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.497-32840A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141404768 | ||||||
| chr7:141404823
|
G | C | 2 | a0001c0001t0005g0008a0001c0001t0023g0018 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-32785G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141404823 | ||||||
| chr7:141405077
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0025g0010 | 3 | HG02486.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.497-32531G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141405077 | ||||||
| chr7:141405456
|
G | A | 6 | a0001c0002t0013g0059a0001c0002t0031g0063a0001c0002t0036g0069others(3): Show | 6 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-32152G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141405456 | ||||||
| chr7:141405982
|
C | T | 1 | a0001c0001t0003g0020 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.497-31626C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141405982 | ||||||
| chr7:141406752
|
T | G | 13 | a0001c0001t0002g0027a0001c0001t0004g0023a0001c0001t0010g0021others(10): Show | 13 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.497-30856T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141406752 | ||||||
| chr7:141406756
|
A | G | 2 | a0001c0001t0005g0008a0001c0001t0023g0018 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-30852A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141406756 | ||||||
| chr7:141406763
|
C | G | 2 | a0001c0001t0008g0004a0001c0001t0009g0078 | 2 | HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.497-30845C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141406763 | ||||||
| chr7:141406917
|
C | T | 1 | a0001c0002t0010g0066 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.497-30691C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141406917 | ||||||
| chr7:141406918
|
A | G | 2 | a0001c0002t0010g0066a0001c0002t0027g0051 | 2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.497-30690A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141406918 | ||||||
| chr7:141406982
|
A | G | 1 | a0001c0002t0005g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.497-30626A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141406982 | ||||||
| chr7:141407107
|
A | G | 1 | a0001c0002t0001g0064 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.497-30501A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141407107 | ||||||
| chr7:141407797
|
T | G | 1 | a0001c0002t0001g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.497-29811T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141407797 | ||||||
| chr7:141407838
|
A | G | 1 | a0001c0005t0001g0005 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.497-29770A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141407838 | ||||||
| chr7:141408200
|
C | T | 2 | a0001c0001t0005g0008a0001c0001t0023g0018 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-29408C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141408200 | ||||||
| chr7:141408457
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0005g0008others(2): Show | 5 | HG02486.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.497-29151A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141408457 | ||||||
| chr7:141408644
|
G | A | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-28964G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141408644 | ||||||
| chr7:141408646
|
G | A | 1 | a0001c0001t0011g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.497-28962G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141408646 | ||||||
| chr7:141409731
|
C | CT | 9 | a0001c0001t0001g0012a0001c0001t0005g0008a0001c0001t0011g0016others(6): Show | 9 | HG01106.hp2 HG01243.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-27864dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141409731 | |||||
| chr7:141409997
|
C | T | 6 | a0001c0002t0013g0059a0001c0002t0031g0063a0001c0002t0036g0069others(3): Show | 6 | HG01255.hp2 HG01256.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-27611C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141409997 | ||||||
| chr7:141410346
|
G | A | 19 | a0001c0001t0001g0012a0001c0001t0002g0027a0001c0001t0006g0017others(16): Show | 19 | HG01106.hp2 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.497-27262G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141410346 | ||||||
| chr7:141410415
|
T | C | 1 | a0001c0003t0019g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497-27193T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141410415 | ||||||
| chr7:141410417
|
C | G | 1 | a0001c0003t0019g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497-27191C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141410417 | ||||||
| chr7:141410422
|
G | GT | 78 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(75): Show | 78 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(75): Show |
intron_variant | MODIFIER | c.497-27178dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141410422 | |||||
| chr7:141410453
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.497-27155T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141410453 | ||||||
| chr7:141410578
|
G | A | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-27030G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141410578 | ||||||
| chr7:141410994
|
C | T | 15 | a0001c0001t0004g0023a0001c0001t0004g0029a0001c0001t0006g0017others(12): Show | 15 | HG00544.hp2 HG01255.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.497-26614C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141410994 | ||||||
| chr7:141411083
|
T | TAAAAAGA others(142): Show |
1 | a0001c0001t0004g0023 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.497-26486_497-2648 others(153): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141411083 | |||||
| chr7:141411112
|
G | A | 1 | a0001c0001t0004g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.497-26496G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141411112 | ||||||
| chr7:141411123
|
G | A | 23 | a0001c0001t0001g0012a0001c0001t0003g0020a0001c0001t0005g0014others(20): Show | 23 | HG00544.hp2 HG01106.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.497-26485G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141411123 | ||||||
| chr7:141411162
|
G | A | 1 | a0001c0001t0035g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.497-26446G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141411162 | ||||||
| chr7:141411208
|
A | C | 42 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0003g0007others(39): Show | 42 | HG01106.hp2 HG01243.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.497-26400A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141411208 | ||||||
| chr7:141411230
|
T | G | 1 | a0001c0002t0001g0057 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.497-26378T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141411230 | ||||||
| chr7:141411844
|
G | C | 1 | a0001c0001t0035g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.497-25764G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141411844 | ||||||
| chr7:141411936
|
G | A | 1 | a0001c0001t0022g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.497-25672G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141411936 | ||||||
| chr7:141412006
|
T | G | 18 | a0001c0001t0006g0025a0001c0001t0007g0011a0001c0001t0011g0016others(15): Show | 18 | HG00544.hp2 HG01243.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.497-25602T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141412006 | ||||||
| chr7:141413103
|
A | G | 1 | a0001c0001t0002g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.497-24505A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141413103 | ||||||
| chr7:141413564
|
C | A | 2 | a0001c0002t0013g0059a0001c0002t0036g0069 | 2 | HG01255.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.497-24044C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141413564 | ||||||
| chr7:141413839
|
CTTA | C | 18 | a0001c0001t0001g0038a0001c0001t0006g0025a0001c0001t0011g0016others(15): Show | 18 | HG00544.hp2 HG01243.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.497-23763_497-2376 others(7): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141413839 | |||||
| chr7:141414063
|
TCCAAAAA others(312): Show |
T | 55 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0038others(52): Show | 55 | HG00544.hp1 HG00544.hp2 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.497-23527_497-2320 others(4): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141414063 | |||||
| chr7:141414512
|
G | GCAAT | 20 | a0001c0001t0001g0038a0001c0001t0001g0080a0001c0001t0006g0025others(17): Show | 20 | HG00544.hp1 HG00544.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.497-23095_497-2309 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141414512 | |||||
| chr7:141414551
|
C | T | 1 | a0001c0002t0002g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.497-23057C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141414551 | ||||||
| chr7:141414662
|
T | C | 1 | a0001c0002t0042g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.497-22946T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141414662 | ||||||
| chr7:141415462
|
G | A | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.497-22146G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141415462 | ||||||
| chr7:141416090
|
G | C | 22 | a0001c0001t0001g0038a0001c0001t0006g0025a0001c0001t0011g0016others(19): Show | 22 | HG00544.hp2 HG01243.hp1 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.497-21518G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141416090 | ||||||
| chr7:141416195
|
A | G | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.497-21413A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141416195 | ||||||
| chr7:141416300
|
G | A | 3 | a0001c0001t0012g0036a0001c0002t0012g0045a0001c0002t0013g0047 | 3 | HG00544.hp2 HG02083.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.497-21308G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141416300 | ||||||
| chr7:141416453
|
C | G | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.497-21155C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141416453 | ||||||
| chr7:141416468
|
G | A | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.497-21140G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141416468 | ||||||
| chr7:141416625
|
A | G | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.497-20983A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141416625 | ||||||
| chr7:141416980
|
G | A | 10 | a0001c0001t0001g0038a0001c0001t0011g0016a0001c0001t0012g0036others(7): Show | 10 | HG00544.hp2 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-20628G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141416980 | ||||||
| chr7:141417053
|
C | T | 2 | a0001c0001t0015g0028a0001c0001t0023g0018 | 2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-20555C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141417053 | ||||||
| chr7:141417088
|
A | C | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.497-20520A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141417088 | ||||||
| chr7:141417145
|
C | G | 8 | a0001c0001t0006g0025a0001c0001t0014g0033a0001c0001t0014g0039others(5): Show | 8 | HG01243.hp1 HG02615.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.497-20463C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141417145 | ||||||
| chr7:141417222
|
C | T | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.497-20386C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141417222 | ||||||
| chr7:141417496
|
G | GTGAA | 4 | a0001c0001t0009g0078a0001c0001t0029g0026a0001c0002t0005g0049others(1): Show | 4 | HG01884.hp2 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-20097_497-2009 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141417496 | |||||
| chr7:141417541
|
G | A | 9 | a0001c0001t0003g0007a0001c0001t0006g0017a0001c0001t0008g0030others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-20067G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141417541 | ||||||
| chr7:141417555
|
A | G | 1 | a0001c0001t0007g0011 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.497-20053A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141417555 | ||||||
| chr7:141417574
|
C | T | 3 | a0001c0001t0015g0028a0001c0001t0023g0018a0001c0001t0038g0034 | 3 | HG02922.hp1 HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-20034C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141417574 | ||||||
| chr7:141417658
|
C | T | 10 | a0001c0001t0003g0007a0001c0001t0005g0008a0001c0001t0006g0017others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-19950C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141417658 | ||||||
| chr7:141417828
|
C | T | 2 | a0001c0001t0021g0077a0001c0002t0010g0066 | 2 | HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.497-19780C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141417828 | ||||||
| chr7:141417839
|
T | C | 22 | a0001c0001t0001g0038a0001c0001t0006g0025a0001c0001t0011g0016others(19): Show | 22 | HG00544.hp2 HG01243.hp1 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.497-19769T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141417839 | ||||||
| chr7:141417840
|
G | A | 21 | a0001c0001t0001g0038a0001c0001t0006g0025a0001c0001t0011g0016others(18): Show | 21 | HG00544.hp2 HG01243.hp1 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.497-19768G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141417840 | ||||||
| chr7:141417944
|
A | G | 18 | a0001c0001t0001g0038a0001c0001t0006g0025a0001c0001t0011g0016others(15): Show | 18 | HG00544.hp2 HG01243.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.497-19664A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141417944 | ||||||
| chr7:141417966
|
T | C | 1 | a0001c0002t0031g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.497-19642T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141417966 | ||||||
| chr7:141418021
|
C | A | 18 | a0001c0001t0001g0038a0001c0001t0006g0025a0001c0001t0011g0016others(15): Show | 18 | HG00544.hp2 HG01243.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.497-19587C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141418021 | ||||||
| chr7:141418048
|
A | G | 1 | a0001c0001t0006g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.497-19560A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141418048 | ||||||
| chr7:141418509
|
A | G | 3 | a0001c0001t0015g0028a0001c0001t0023g0018a0001c0001t0038g0034 | 3 | HG02922.hp1 HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.497-19099A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141418509 | ||||||
| chr7:141418575
|
A | C | 32 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0080others(29): Show | 32 | HG00544.hp1 HG01106.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.497-19033A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141418575 | ||||||
| chr7:141418851
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0035g0079 | 2 | HG02258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.497-18757G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141418851 | ||||||
| chr7:141418905
|
T | TTTTA | 55 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0038others(52): Show | 55 | HG00544.hp1 HG00544.hp2 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.497-18687_497-1868 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141418905 | |||||
| chr7:141419202
|
G | A | 1 | a0001c0001t0006g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.497-18406G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141419202 | ||||||
| chr7:141419343
|
A | G | 23 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0080others(20): Show | 23 | HG00544.hp1 HG01106.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.497-18265A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141419343 | ||||||
| chr7:141419628
|
T | C | 55 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0038others(52): Show | 55 | HG00544.hp1 HG00544.hp2 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.497-17980T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141419628 | ||||||
| chr7:141419697
|
A | G | 18 | a0001c0001t0001g0038a0001c0001t0006g0025a0001c0001t0011g0016others(15): Show | 18 | HG00544.hp2 HG01243.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.497-17911A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141419697 | ||||||
| chr7:141420192
|
GC | G | 9 | a0001c0001t0001g0038a0001c0001t0011g0016a0001c0001t0012g0036others(6): Show | 9 | HG00544.hp2 HG01978.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-17407delC | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141420192 | |||||
| chr7:141420848
|
G | A | 1 | a0001c0002t0042g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.497-16760G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141420848 | ||||||
| chr7:141420863
|
G | C | 27 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0038others(24): Show | 27 | HG00544.hp1 HG01106.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.497-16745G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141420863 | ||||||
| chr7:141420992
|
T | G | 1 | a0001c0003t0001g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.497-16616T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141420992 | ||||||
| chr7:141421269
|
T | G | 6 | a0001c0001t0014g0033a0001c0001t0014g0039a0001c0001t0028g0022others(3): Show | 6 | HG01243.hp1 HG02258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-16339T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141421269 | ||||||
| chr7:141421320
|
T | C | 4 | a0001c0001t0003g0007a0001c0001t0033g0031a0001c0002t0003g0052others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-16288T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141421320 | ||||||
| chr7:141421488
|
A | C | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-16120A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141421488 | ||||||
| chr7:141421596
|
G | C | 1 | a0001c0001t0006g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.497-16012G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141421596 | ||||||
| chr7:141421784
|
A | T | 3 | a0001c0001t0012g0036a0001c0002t0012g0045a0001c0002t0013g0047 | 3 | HG00544.hp2 HG02083.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.497-15824A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141421784 | ||||||
| chr7:141422018
|
A | G | 1 | a0001c0002t0042g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.497-15590A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141422018 | ||||||
| chr7:141422148
|
T | C | 1 | a0001c0002t0027g0051 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.497-15460T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141422148 | ||||||
| chr7:141422202
|
C | T | 34 | a0001c0001t0001g0015a0001c0001t0002g0027a0001c0001t0004g0023others(31): Show | 34 | HG00544.hp2 HG01255.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.497-15406C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141422202 | ||||||
| chr7:141422403
|
C | A | 2 | a0001c0001t0038g0034a0001c0002t0027g0051 | 2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.497-15205C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141422403 | ||||||
| chr7:141422564
|
G | C | 41 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0002g0027others(38): Show | 41 | HG00544.hp2 HG01106.hp2 HG01255.hp1 others(38): Show |
intron_variant | MODIFIER | c.497-15044G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141422564 | ||||||
| chr7:141422580
|
G | C | 41 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0002g0027others(38): Show | 41 | HG00544.hp2 HG01106.hp2 HG01255.hp1 others(38): Show |
intron_variant | MODIFIER | c.497-15028G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141422580 | ||||||
| chr7:141422598
|
CTCTGGCC others(5): Show |
C | 31 | a0001c0001t0001g0015a0001c0001t0002g0027a0001c0001t0004g0023others(28): Show | 31 | HG01255.hp1 HG01261.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.497-15009_497-1499 others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141422598 | ||||||
| chr7:141422612
|
T | G | 31 | a0001c0001t0001g0015a0001c0001t0002g0027a0001c0001t0004g0023others(28): Show | 31 | HG01255.hp1 HG01261.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.497-14996T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141422612 | ||||||
| chr7:141422632
|
C | G | 1 | a0001c0001t0004g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.497-14976C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141422632 | ||||||
| chr7:141422896
|
G | A | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.497-14712G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141422896 | ||||||
| chr7:141422968
|
G | A | 36 | a0001c0001t0001g0015a0001c0001t0002g0027a0001c0001t0004g0023others(33): Show | 36 | HG00544.hp2 HG01255.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.497-14640G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141422968 | ||||||
| chr7:141423035
|
T | G | 1 | a0001c0001t0002g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.497-14573T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141423035 | ||||||
| chr7:141423096
|
G | A | 2 | a0001c0001t0006g0025a0001c0002t0001g0042 | 2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.497-14512G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141423096 | ||||||
| chr7:141423214
|
G | C | 1 | a0001c0001t0035g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.497-14394G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141423214 | ||||||
| chr7:141423805
|
G | GT | 17 | a0001c0001t0001g0038a0001c0001t0003g0007a0001c0001t0006g0017others(14): Show | 17 | HG00544.hp2 HG01891.hp2 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.497-13782dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141423805 | |||||
| chr7:141423805
|
GT | G | 24 | a0001c0001t0001g0015a0001c0001t0004g0023a0001c0001t0004g0024others(21): Show | 24 | HG01255.hp1 HG01884.hp2 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.497-13782delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141423805 | |||||
| chr7:141423811
|
T | G | 1 | a0001c0002t0009g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.497-13797T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141423811 | ||||||
| chr7:141423975
|
A | AT | 9 | a0001c0001t0001g0012a0001c0001t0004g0023a0001c0001t0006g0025others(6): Show | 9 | HG01106.hp2 HG01952.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-13619dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141423975 | |||||
| chr7:141424088
|
G | A | 1 | a0001c0002t0001g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.497-13520G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141424088 | ||||||
| chr7:141424151
|
C | T | 1 | a0001c0001t0014g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.497-13457C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141424151 | ||||||
| chr7:141424384
|
C | T | 1 | a0001c0002t0042g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.497-13224C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141424384 | ||||||
| chr7:141424486
|
G | A | 16 | a0001c0001t0001g0038a0001c0001t0003g0007a0001c0001t0006g0017others(13): Show | 16 | HG01891.hp2 HG01978.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.497-13122G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141424486 | ||||||
| chr7:141424534
|
T | C | 55 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(52): Show | 55 | HG00544.hp2 HG01106.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.497-13074T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141424534 | ||||||
| chr7:141424560
|
T | G | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.497-13048T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141424560 | ||||||
| chr7:141424678
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.497-12930C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141424678 | ||||||
| chr7:141424940
|
T | C | 1 | a0001c0002t0042g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.497-12668T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141424940 | ||||||
| chr7:141425029
|
T | C | 1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.497-12579T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141425029 | ||||||
| chr7:141425712
|
C | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.497-11896C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141425712 | ||||||
| chr7:141425778
|
T | A | 26 | a0001c0001t0001g0015a0001c0001t0002g0027a0001c0001t0004g0024others(23): Show | 26 | HG01255.hp1 HG01261.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.497-11830T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141425778 | ||||||
| chr7:141425796
|
T | C | 55 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(52): Show | 55 | HG00544.hp2 HG01106.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.497-11812T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141425796 | ||||||
| chr7:141425917
|
CT | C | 2 | a0001c0001t0009g0078a0001c0002t0040g0050 | 2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.497-11690delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141425917 | ||||||
| chr7:141426001
|
A | G | 6 | a0001c0001t0004g0023a0001c0001t0012g0036a0001c0002t0001g0042others(3): Show | 6 | HG00544.hp2 HG01952.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-11607A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141426001 | ||||||
| chr7:141426141
|
A | G | 1 | a0001c0001t0008g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.497-11467A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141426141 | ||||||
| chr7:141426968
|
G | A | 80 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(77): Show | 80 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.497-10640G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141426968 | ||||||
| chr7:141427104
|
A | T | 1 | a0001c0002t0024g0002 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.497-10504A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141427104 | ||||||
| chr7:141427147
|
C | G | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-10461C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141427147 | ||||||
| chr7:141427440
|
A | G | 1 | a0001c0001t0004g0023 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.497-10168A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141427440 | ||||||
| chr7:141427758
|
A | G | 26 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0002g0019others(23): Show | 26 | HG01106.hp2 HG01891.hp2 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.497-9850A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141427758 | ||||||
| chr7:141427823
|
A | G | 26 | a0001c0001t0001g0015a0001c0001t0002g0027a0001c0001t0004g0024others(23): Show | 26 | HG01255.hp1 HG01261.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.497-9785A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141427823 | ||||||
| chr7:141428362
|
C | G | 1 | a0001c0001t0044g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.497-9246C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141428362 | ||||||
| chr7:141428368
|
C | CA | 5 | a0001c0001t0005g0014a0001c0001t0012g0036a0001c0001t0028g0022others(2): Show | 5 | HG01256.hp2 HG02523.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-9224dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141428368 | |||||
| chr7:141428383
|
AAG | A | 6 | a0001c0001t0007g0011a0001c0001t0044g0001a0001c0002t0007g0053others(3): Show | 6 | HG02602.hp1 HG02602.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-9223_497-9222d others(4): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141428383 | |||||
| chr7:141428384
|
AG | A | 32 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(29): Show | 32 | HG01106.hp2 HG01261.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.497-9223delG | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141428384 | ||||||
| chr7:141428385
|
G | A | 40 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0003g0020others(37): Show | 40 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.497-9223G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141428385 | ||||||
| chr7:141428387
|
A | G | 21 | a0001c0001t0001g0038a0001c0001t0002g0019a0001c0001t0003g0007others(18): Show | 21 | HG01891.hp2 HG01978.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.497-9221A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141428387 | ||||||
| chr7:141428412
|
A | C | 1 | a0001c0002t0024g0002 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.497-9196A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141428412 | ||||||
| chr7:141428527
|
C | T | 1 | a0001c0001t0014g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.497-9081C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141428527 | ||||||
| chr7:141428759
|
C | T | 1 | a0001c0003t0018g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.497-8849C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141428759 | ||||||
| chr7:141429043
|
A | T | 1 | a0001c0001t0001g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.497-8565A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141429043 | ||||||
| chr7:141429308
|
T | TAC | 3 | a0001c0001t0002g0027a0001c0001t0035g0079a0001c0002t0001g0042 | 3 | HG02258.hp1 HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.497-8269_497-8268d others(4): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141429308 | |||||
| chr7:141429308
|
T | TACAC | 2 | a0001c0001t0004g0023a0001c0002t0002g0043 | 2 | HG01952.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.497-8271_497-8268d others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141429308 | |||||
| chr7:141429308
|
T | TACACAC | 8 | a0001c0001t0016g0037a0001c0001t0020g0006a0001c0001t0022g0013others(5): Show | 8 | HG01255.hp1 HG01261.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.497-8273_497-8268d others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141429308 | |||||
| chr7:141429308
|
T | TACACACA others(1): Show |
12 | a0001c0001t0001g0015a0001c0001t0004g0024a0001c0001t0005g0014others(9): Show | 12 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.497-8275_497-8268d others(10): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141429308 | |||||
| chr7:141429308
|
T | TACACACA others(3): Show |
3 | a0001c0001t0004g0029a0001c0001t0007g0011a0001c0002t0007g0073 | 3 | HG02602.hp1 HG03453.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.497-8277_497-8268d others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141429308 | |||||
| chr7:141429308
|
T | TACACACA others(5): Show |
3 | a0001c0001t0005g0008a0001c0002t0026g0041a0001c0002t0031g0063 | 3 | HG02572.hp1 HG02602.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.497-8279_497-8268d others(14): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141429308 | |||||
| chr7:141429308
|
TAC | T | 3 | a0001c0001t0038g0034a0001c0001t0044g0001a0001c0002t0027g0051 | 3 | HG02922.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.497-8269_497-8268d others(4): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141429308 | |||||
| chr7:141429308
|
TACAC | T | 24 | a0001c0001t0001g0012a0001c0001t0001g0080a0001c0001t0003g0020others(21): Show | 24 | HG00544.hp1 HG00544.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.497-8271_497-8268d others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141429308 | |||||
| chr7:141429308
|
TACACACA others(7): Show |
T | 20 | a0001c0001t0001g0038a0001c0001t0002g0019a0001c0001t0003g0007others(17): Show | 20 | HG01891.hp2 HG01978.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.497-8281_497-8268d others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141429308 | |||||
| chr7:141429318
|
C | A | 1 | a0001c0001t0034g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.497-8290C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141429318 | ||||||
| chr7:141429341
|
T | C | 1 | a0001c0002t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.497-8267T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141429341 | ||||||
| chr7:141429666
|
C | T | 34 | a0001c0001t0001g0015a0001c0001t0002g0027a0001c0001t0004g0023others(31): Show | 34 | HG00544.hp2 HG01255.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.497-7942C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141429666 | ||||||
| chr7:141430059
|
T | C | 60 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(57): Show | 60 | HG00544.hp2 HG01106.hp2 HG01255.hp1 others(57): Show |
intron_variant | MODIFIER | c.497-7549T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141430059 | ||||||
| chr7:141430340
|
G | C | 55 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0002g0019others(52): Show | 55 | HG00544.hp2 HG01255.hp1 HG01261.hp1 others(52): Show |
intron_variant | MODIFIER | c.497-7268G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141430340 | ||||||
| chr7:141430516
|
G | A | 1 | a0001c0001t0035g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.497-7092G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141430516 | ||||||
| chr7:141430546
|
C | G | 17 | a0001c0001t0001g0038a0001c0001t0002g0019a0001c0001t0003g0007others(14): Show | 17 | HG01891.hp2 HG01978.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.497-7062C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141430546 | ||||||
| chr7:141430554
|
G | A | 1 | a0001c0001t0015g0028 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.497-7054G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141430554 | ||||||
| chr7:141430555
|
G | T | 1 | a0001c0002t0027g0051 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.497-7053G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141430555 | ||||||
| chr7:141430665
|
G | A | 34 | a0001c0001t0001g0015a0001c0001t0002g0027a0001c0001t0004g0023others(31): Show | 34 | HG00544.hp2 HG01255.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.497-6943G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141430665 | ||||||
| chr7:141431090
|
G | A | 2 | a0001c0001t0001g0012a0001c0002t0002g0043 | 2 | HG01106.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.497-6518G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141431090 | ||||||
| chr7:141431132
|
G | A | 20 | a0001c0001t0001g0038a0001c0001t0002g0019a0001c0001t0003g0007others(17): Show | 20 | HG01891.hp2 HG01978.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.497-6476G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141431132 | ||||||
| chr7:141431170
|
G | GT | 25 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0002g0019others(22): Show | 25 | HG01106.hp2 HG01891.hp2 HG01978.hp1 others(22): Show |
intron_variant | MODIFIER | c.497-6426dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141431170 | |||||
| chr7:141431473
|
G | A | 3 | a0001c0001t0012g0036a0001c0002t0012g0045a0001c0002t0013g0047 | 3 | HG00544.hp2 HG02083.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.497-6135G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141431473 | ||||||
| chr7:141431634
|
C | CT | 2 | a0001c0002t0001g0042a0001c0002t0042g0054 | 2 | NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.497-5973dupT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141431634 | |||||
| chr7:141431875
|
T | C | 61 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(58): Show | 61 | HG00544.hp2 HG01106.hp2 HG01255.hp1 others(58): Show |
intron_variant | MODIFIER | c.497-5733T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141431875 | ||||||
| chr7:141431910
|
A | G | 80 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(77): Show | 80 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.497-5698A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141431910 | ||||||
| chr7:141432049
|
A | G | 3 | a0001c0001t0012g0036a0001c0002t0012g0045a0001c0002t0013g0047 | 3 | HG00544.hp2 HG02083.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.497-5559A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141432049 | ||||||
| chr7:141432146
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0001g0012a0001c0001t0008g0004a0001c0001t0035g0079others(1): Show | 4 | HG01106.hp2 HG02258.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-5445_497-5434d others(14): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141432146 | |||||
| chr7:141432146
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0006g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.497-5446_497-5434d others(15): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141432146 | |||||
| chr7:141432146
|
C | CTTTTTTT others(7): Show |
2 | a0001c0002t0009g0060a0001c0002t0042g0054 | 2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.497-5447_497-5434d others(16): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141432146 | |||||
| chr7:141432146
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0038g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.497-5448_497-5434d others(17): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141432146 | |||||
| chr7:141432146
|
C | CTTTTTTT others(14): Show |
1 | a0001c0002t0027g0051 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.497-5454_497-5434d others(23): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141432146 | |||||
| chr7:141432146
|
CTT | C | 4 | a0001c0002t0001g0076a0001c0002t0007g0073a0001c0002t0016g0072others(1): Show | 4 | HG01261.hp2 HG02602.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-5435_497-5434d others(4): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141432146 | |||||
| chr7:141432146
|
CTTT | C | 39 | a0001c0001t0001g0015a0001c0001t0001g0080a0001c0001t0002g0027others(36): Show | 39 | HG00544.hp1 HG01106.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.497-5436_497-5434d others(5): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141432146 | |||||
| chr7:141432146
|
CTTTTTTT others(3): Show |
C | 18 | a0001c0001t0001g0038a0001c0001t0002g0019a0001c0001t0003g0007others(15): Show | 18 | HG01891.hp2 HG01978.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.497-5443_497-5434d others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141432146 | |||||
| chr7:141432146
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.497-5444_497-5434d others(13): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 141432146 | |||||
| chr7:141432259
|
A | G | 1 | a0001c0002t0042g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.497-5349A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141432259 | ||||||
| chr7:141432299
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0008g0004a0001c0001t0038g0034others(2): Show | 5 | HG01106.hp2 HG02922.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-5309G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141432299 | ||||||
| chr7:141432357
|
G | T | 1 | a0001c0002t0037g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.497-5251G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141432357 | ||||||
| chr7:141432761
|
C | G | 5 | a0001c0001t0001g0012a0001c0001t0008g0004a0001c0001t0038g0034others(2): Show | 5 | HG01106.hp2 HG02922.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-4847C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141432761 | ||||||
| chr7:141432827
|
C | T | 34 | a0001c0001t0001g0015a0001c0001t0002g0027a0001c0001t0004g0023others(31): Show | 34 | HG00544.hp2 HG01255.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.497-4781C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141432827 | ||||||
| chr7:141432873
|
G | T | 2 | a0001c0002t0037g0075a0001c0003t0001g0055 | 2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.497-4735G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141432873 | ||||||
| chr7:141433043
|
T | C | 64 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(61): Show | 64 | HG00544.hp2 HG01106.hp2 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.497-4565T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141433043 | ||||||
| chr7:141433094
|
A | G | 1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.497-4514A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141433094 | ||||||
| chr7:141433129
|
C | T | 1 | a0001c0003t0018g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.497-4479C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141433129 | ||||||
| chr7:141433321
|
T | G | 60 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0038others(57): Show | 60 | HG00544.hp2 HG01106.hp2 HG01255.hp1 others(57): Show |
intron_variant | MODIFIER | c.497-4287T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141433321 | ||||||
| chr7:141433345
|
AG | A | 6 | a0001c0001t0002g0027a0001c0001t0004g0024a0001c0001t0004g0029others(3): Show | 6 | HG01261.hp2 HG01891.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-4262delG | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141433345 | ||||||
| chr7:141433349
|
T | C | 6 | a0001c0001t0002g0027a0001c0001t0004g0024a0001c0001t0004g0029others(3): Show | 6 | HG01261.hp2 HG01891.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-4259T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141433349 | ||||||
| chr7:141433551
|
G | A | 3 | a0001c0001t0012g0036a0001c0002t0012g0045a0001c0002t0013g0047 | 3 | HG00544.hp2 HG02083.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.497-4057G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141433551 | ||||||
| chr7:141433837
|
G | A | 4 | a0001c0001t0002g0019a0001c0001t0009g0078a0001c0001t0010g0021others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-3771G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141433837 | ||||||
| chr7:141434004
|
C | T | 36 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0002g0027others(33): Show | 36 | HG00544.hp2 HG01106.hp2 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.497-3604C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141434004 | ||||||
| chr7:141434155
|
C | T | 1 | a0001c0002t0009g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.497-3453C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141434155 | ||||||
| chr7:141434320
|
A | G | 1 | a0001c0001t0038g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.497-3288A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141434320 | ||||||
| chr7:141434476
|
T | A | 33 | a0001c0001t0001g0015a0001c0001t0002g0027a0001c0001t0004g0023others(30): Show | 33 | HG00544.hp2 HG01255.hp1 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.497-3132T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141434476 | ||||||
| chr7:141434483
|
T | A | 1 | a0001c0001t0004g0024 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.497-3125T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141434483 | ||||||
| chr7:141434575
|
C | T | 12 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0014g0033others(9): Show | 12 | HG00544.hp1 HG01243.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.497-3033C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141434575 | ||||||
| chr7:141434624
|
A | T | 38 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0002g0027others(35): Show | 38 | HG00544.hp2 HG01106.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.497-2984A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141434624 | ||||||
| chr7:141434770
|
C | G | 39 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0002g0027others(36): Show | 39 | HG00544.hp2 HG01106.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.497-2838C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141434770 | ||||||
| chr7:141435143
|
TC | T | 10 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0014g0033others(7): Show | 10 | HG00544.hp1 HG01243.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-2464delC | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141435143 | ||||||
| chr7:141435231
|
A | G | 1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.497-2377A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141435231 | ||||||
| chr7:141435314
|
G | A | 32 | a0001c0001t0001g0080a0001c0001t0002g0027a0001c0001t0004g0024others(29): Show | 32 | HG00544.hp1 HG00544.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.497-2294G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141435314 | ||||||
| chr7:141435329
|
T | C | 1 | a0001c0001t0038g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.497-2279T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141435329 | ||||||
| chr7:141435366
|
A | G | 1 | a0001c0002t0031g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.497-2242A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141435366 | ||||||
| chr7:141435560
|
A | G | 17 | a0001c0001t0003g0007a0001c0001t0004g0023a0001c0001t0004g0024others(14): Show | 17 | HG01261.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.497-2048A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141435560 | ||||||
| chr7:141435782
|
G | A | 1 | a0001c0002t0031g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.497-1826G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141435782 | ||||||
| chr7:141435975
|
G | C | 1 | a0001c0003t0019g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.497-1633G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141435975 | ||||||
| chr7:141435984
|
C | G | 3 | a0001c0001t0003g0007a0001c0002t0003g0052a0001c0002t0030g0067 | 3 | HG01891.hp2 HG02109.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.497-1624C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141435984 | ||||||
| chr7:141435993
|
T | A | 1 | a0001c0001t0004g0023 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.497-1615T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141435993 | ||||||
| chr7:141436218
|
A | G | 1 | a0001c0001t0033g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.497-1390A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141436218 | ||||||
| chr7:141436424
|
G | A | 32 | a0001c0001t0002g0019a0001c0001t0003g0020a0001c0001t0004g0023others(29): Show | 32 | HG01243.hp1 HG01255.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.497-1184G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141436424 | ||||||
| chr7:141436498
|
G | A | 1 | a0001c0001t0023g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.497-1110G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141436498 | ||||||
| chr7:141436553
|
G | A | 1 | a0001c0002t0026g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.497-1055G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141436553 | ||||||
| chr7:141436665
|
G | A | 1 | a0001c0002t0027g0051 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.497-943G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141436665 | ||||||
| chr7:141436772
|
A | C | 2 | a0001c0001t0011g0016a0002c0006t0039g0061 | 2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.497-836A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141436772 | ||||||
| chr7:141436803
|
A | C | 4 | a0001c0001t0003g0020a0001c0001t0004g0023a0001c0001t0004g0024others(1): Show | 4 | HG01952.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-805A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141436803 | ||||||
| chr7:141436812
|
C | T | 1 | a0001c0001t0035g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.497-796C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141436812 | ||||||
| chr7:141437105
|
G | A | 2 | a0001c0002t0026g0041a0001c0002t0027g0051 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.497-503G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141437105 | ||||||
| chr7:141437184
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.497-424G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141437184 | ||||||
| chr7:141437204
|
A | G | 71 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(68): Show | 71 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(68): Show |
intron_variant | MODIFIER | c.497-404A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141437204 | ||||||
| chr7:141437331
|
G | A | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.497-277G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 2/3 | chr7 | 141437331 | ||||||
| chr7:141437754
|
A | G | 71 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(68): Show | 71 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(68): Show |
intron_variant | MODIFIER | c.634+9A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141437754 | ||||||
| chr7:141437756
|
G | A | 26 | a0001c0001t0001g0035a0001c0001t0002g0027a0001c0001t0003g0007others(23): Show | 26 | HG01106.hp1 HG01243.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.634+11G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141437756 | ||||||
| chr7:141438052
|
G | A | 1 | a0001c0001t0022g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.634+307G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141438052 | ||||||
| chr7:141438146
|
T | C | 2 | a0001c0001t0004g0029a0001c0001t0029g0026 | 2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.634+401T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141438146 | ||||||
| chr7:141438170
|
A | G | 7 | a0001c0001t0003g0007a0001c0001t0003g0020a0001c0001t0004g0023others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+425A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141438170 | ||||||
| chr7:141438208
|
C | G | 33 | a0001c0001t0001g0035a0001c0001t0002g0019a0001c0001t0002g0027others(30): Show | 33 | HG01106.hp1 HG01243.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.634+463C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141438208 | ||||||
| chr7:141438251
|
A | G | 45 | a0001c0001t0001g0015a0001c0001t0002g0019a0001c0001t0005g0008others(42): Show | 45 | HG00544.hp2 HG01255.hp1 HG01255.hp2 others(42): Show |
intron_variant | MODIFIER | c.634+506A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141438251 | ||||||
| chr7:141438404
|
T | C | 65 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(62): Show | 65 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(62): Show |
intron_variant | MODIFIER | c.634+659T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141438404 | ||||||
| chr7:141438444
|
C | T | 3 | a0001c0001t0015g0028a0001c0002t0015g0056a0001c0002t0024g0002 | 3 | HG03225.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.634+699C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141438444 | ||||||
| chr7:141438556
|
G | A | 9 | a0001c0001t0006g0017a0001c0001t0006g0025a0001c0001t0007g0011others(6): Show | 9 | HG01255.hp1 HG02083.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.634+811G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141438556 | ||||||
| chr7:141438696
|
T | TA | 10 | a0001c0001t0001g0015a0001c0001t0005g0014a0001c0002t0001g0042others(7): Show | 10 | HG00544.hp2 HG01952.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.634+981dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141438696 | |||||
| chr7:141438696
|
T | TAA | 9 | a0001c0001t0006g0025a0001c0001t0022g0013a0001c0001t0023g0018others(6): Show | 9 | HG01261.hp1 HG02027.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.634+980_634+981dup others(2): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141438696 | |||||
| chr7:141438696
|
T | TAAA | 14 | a0001c0001t0006g0017a0001c0001t0007g0011a0001c0001t0008g0030others(11): Show | 14 | HG01243.hp1 HG01255.hp2 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.634+979_634+981dup others(3): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141438696 | |||||
| chr7:141438696
|
T | TAAAA | 5 | a0001c0001t0009g0078a0001c0001t0028g0022a0001c0002t0010g0066others(2): Show | 5 | HG01255.hp1 HG01256.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.634+978_634+981dup others(4): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141438696 | |||||
| chr7:141438696
|
T | TAAAAAAA others(6): Show |
1 | a0001c0001t0021g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.634+969_634+981dup others(13): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141438696 | |||||
| chr7:141438696
|
T | TAAAAAAA others(12): Show |
6 | a0001c0001t0001g0035a0001c0002t0030g0067a0001c0003t0001g0068others(3): Show | 6 | HG01106.hp1 HG01243.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+963_634+981dup others(19): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141438696 | |||||
| chr7:141438696
|
T | TAAAAAAA others(15): Show |
1 | a0001c0001t0003g0007 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.634+960_634+981dup others(22): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141438696 | |||||
| chr7:141438696
|
T | TAAAAAAA others(18): Show |
1 | a0001c0003t0019g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.634+957_634+981dup others(25): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141438696 | |||||
| chr7:141438696
|
TAA | T | 6 | a0001c0001t0004g0029a0001c0001t0029g0026a0001c0001t0035g0079others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+980_634+981del others(2): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141438696 | |||||
| chr7:141438696
|
TAAAAA | T | 5 | a0001c0001t0008g0004a0001c0001t0011g0016a0001c0001t0034g0009others(2): Show | 5 | HG02572.hp2 HG03130.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.634+977_634+981del others(5): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141438696 | |||||
| chr7:141438696
|
TAAAAAAA others(3): Show |
T | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.634+972_634+981del others(10): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141438696 | |||||
| chr7:141438696
|
TAAAAAAA others(5): Show |
T | 2 | a0001c0001t0016g0037a0001c0002t0016g0072 | 2 | HG01261.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.634+970_634+981del others(12): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141438696 | |||||
| chr7:141438698
|
A | T | 1 | a0001c0001t0002g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.634+953A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141438698 | ||||||
| chr7:141438745
|
G | A | 4 | a0001c0001t0002g0019a0001c0001t0025g0010a0001c0002t0002g0043others(1): Show | 4 | HG02486.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+1000G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141438745 | ||||||
| chr7:141438758
|
C | T | 2 | a0001c0001t0008g0004a0001c0001t0034g0009 | 2 | HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.634+1013C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141438758 | ||||||
| chr7:141438841
|
A | C | 5 | a0001c0001t0009g0078a0001c0001t0010g0021a0001c0001t0038g0034others(2): Show | 5 | HG02647.hp2 HG02922.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.634+1096A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141438841 | ||||||
| chr7:141438871
|
G | A | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.634+1126G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141438871 | ||||||
| chr7:141438875
|
C | CAAAAAA | 4 | a0001c0001t0015g0028a0001c0002t0015g0056a0001c0002t0024g0002others(1): Show | 4 | HG02109.hp2 HG03225.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+1134_634+1139d others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141438875 | |||||
| chr7:141438875
|
C | CAAAAAAA | 24 | a0001c0001t0001g0035a0001c0001t0002g0027a0001c0001t0008g0004others(21): Show | 24 | HG01106.hp1 HG01243.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.634+1133_634+1139d others(9): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141438875 | |||||
| chr7:141439079
|
G | A | 26 | a0001c0001t0001g0015a0001c0001t0005g0008a0001c0001t0005g0014others(23): Show | 26 | HG00544.hp2 HG01255.hp1 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.634+1334G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141439079 | ||||||
| chr7:141439198
|
G | A | 1 | a0001c0002t0042g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.634+1453G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141439198 | ||||||
| chr7:141439204
|
C | G | 17 | a0001c0001t0001g0035a0001c0001t0002g0027a0001c0001t0008g0004others(14): Show | 17 | HG01106.hp1 HG01243.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.634+1459C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141439204 | ||||||
| chr7:141439226
|
G | A | 4 | a0001c0001t0010g0021a0001c0001t0038g0034a0001c0002t0008g0003others(1): Show | 4 | HG02922.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+1481G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141439226 | ||||||
| chr7:141439241
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.634+1496A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141439241 | ||||||
| chr7:141439299
|
C | A | 1 | a0001c0002t0042g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.634+1554C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141439299 | ||||||
| chr7:141439429
|
A | G | 5 | a0001c0001t0009g0078a0001c0001t0010g0021a0001c0001t0038g0034others(2): Show | 5 | HG02647.hp2 HG02922.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.634+1684A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141439429 | ||||||
| chr7:141439676
|
G | C | 1 | a0001c0002t0042g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.634+1931G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141439676 | ||||||
| chr7:141439736
|
G | T | 64 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(61): Show | 64 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.634+1991G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141439736 | ||||||
| chr7:141440069
|
G | C | 1 | a0001c0001t0021g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.634+2324G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141440069 | ||||||
| chr7:141440330
|
C | T | 72 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(69): Show | 72 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(69): Show |
intron_variant | MODIFIER | c.634+2585C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141440330 | ||||||
| chr7:141440643
|
G | A | 26 | a0001c0001t0001g0015a0001c0001t0005g0008a0001c0001t0005g0014others(23): Show | 26 | HG00544.hp2 HG01255.hp1 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.634+2898G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141440643 | ||||||
| chr7:141440665
|
T | G | 6 | a0001c0001t0001g0015a0001c0001t0005g0008a0001c0001t0005g0014others(3): Show | 6 | HG02258.hp2 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.634+2920T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141440665 | ||||||
| chr7:141440672
|
C | T | 2 | a0001c0001t0002g0019a0001c0001t0025g0010 | 2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.634+2927C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141440672 | ||||||
| chr7:141440849
|
G | A | 11 | a0001c0001t0002g0019a0001c0001t0008g0004a0001c0001t0021g0077others(8): Show | 11 | HG02486.hp1 HG02572.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.634+3104G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141440849 | ||||||
| chr7:141440875
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.634+3130C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141440875 | ||||||
| chr7:141440970
|
A | G | 8 | a0001c0001t0009g0078a0001c0001t0010g0021a0001c0001t0014g0033others(5): Show | 8 | HG01243.hp1 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.634+3225A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141440970 | ||||||
| chr7:141441177
|
G | C | 49 | a0001c0001t0001g0015a0001c0001t0002g0019a0001c0001t0005g0008others(46): Show | 49 | HG00544.hp2 HG01243.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.634+3432G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141441177 | ||||||
| chr7:141441252
|
C | T | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.634+3507C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141441252 | ||||||
| chr7:141441271
|
A | C | 29 | a0001c0001t0001g0015a0001c0001t0005g0008a0001c0001t0005g0014others(26): Show | 29 | HG00544.hp2 HG01255.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.634+3526A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141441271 | ||||||
| chr7:141441276
|
A | T | 29 | a0001c0001t0001g0015a0001c0001t0005g0008a0001c0001t0005g0014others(26): Show | 29 | HG00544.hp2 HG01255.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.634+3531A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141441276 | ||||||
| chr7:141441301
|
C | T | 2 | a0001c0001t0035g0079a0001c0001t0044g0001 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.634+3556C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141441301 | ||||||
| chr7:141441380
|
T | C | 64 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(61): Show | 64 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.634+3635T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141441380 | ||||||
| chr7:141441391
|
G | C | 29 | a0001c0001t0001g0015a0001c0001t0005g0008a0001c0001t0005g0014others(26): Show | 29 | HG00544.hp2 HG01255.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.634+3646G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141441391 | ||||||
| chr7:141441401
|
A | G | 1 | a0001c0002t0037g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.634+3656A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141441401 | ||||||
| chr7:141441524
|
C | T | 4 | a0001c0001t0009g0078a0001c0001t0010g0021a0001c0002t0008g0003others(1): Show | 4 | HG02647.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+3779C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141441524 | ||||||
| chr7:141441878
|
A | C | 18 | a0001c0001t0001g0035a0001c0001t0002g0027a0001c0001t0014g0033others(15): Show | 18 | HG01106.hp1 HG01243.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.634+4133A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141441878 | ||||||
| chr7:141441999
|
G | A | 2 | a0001c0001t0035g0079a0001c0001t0044g0001 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.634+4254G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141441999 | ||||||
| chr7:141442260
|
A | G | 49 | a0001c0001t0001g0015a0001c0001t0002g0019a0001c0001t0005g0008others(46): Show | 49 | HG00544.hp2 HG01243.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.634+4515A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141442260 | ||||||
| chr7:141442271
|
G | A | 4 | a0001c0001t0008g0004a0001c0001t0034g0009a0001c0002t0040g0050others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+4526G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141442271 | ||||||
| chr7:141442332
|
C | T | 28 | a0001c0001t0001g0015a0001c0001t0005g0008a0001c0001t0005g0014others(25): Show | 28 | HG00544.hp2 HG01255.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.634+4587C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141442332 | ||||||
| chr7:141442679
|
T | C | 12 | a0001c0001t0002g0019a0001c0001t0008g0004a0001c0001t0021g0077others(9): Show | 12 | HG02486.hp1 HG02572.hp1 HG03130.hp1 others(9): Show |
intron_variant | MODIFIER | c.634+4934T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141442679 | ||||||
| chr7:141442723
|
A | T | 4 | a0001c0001t0009g0078a0001c0001t0010g0021a0001c0002t0008g0003others(1): Show | 4 | HG02647.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+4978A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141442723 | ||||||
| chr7:141442797
|
A | G | 34 | a0001c0001t0001g0015a0001c0001t0005g0008a0001c0001t0005g0014others(31): Show | 34 | HG00544.hp2 HG01243.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.634+5052A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141442797 | ||||||
| chr7:141443556
|
A | G | 5 | a0001c0002t0011g0044a0001c0002t0013g0047a0001c0002t0031g0063others(2): Show | 5 | HG00544.hp2 HG01256.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.634+5811A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141443556 | ||||||
| chr7:141443750
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.634+6005G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141443750 | ||||||
| chr7:141444036
|
T | A | 1 | a0001c0001t0021g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.634+6291T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141444036 | ||||||
| chr7:141444174
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0005g0008a0001c0001t0005g0014others(3): Show | 6 | HG02258.hp2 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.634+6429G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141444174 | ||||||
| chr7:141444236
|
A | G | 1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.634+6491A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141444236 | ||||||
| chr7:141444351
|
A | G | 1 | a0001c0002t0013g0059 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.634+6606A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141444351 | ||||||
| chr7:141444563
|
G | A | 1 | a0001c0002t0030g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.634+6818G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141444563 | ||||||
| chr7:141444728
|
T | G | 1 | a0001c0001t0038g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.634+6983T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141444728 | ||||||
| chr7:141444915
|
A | G | 3 | a0001c0001t0014g0033a0001c0001t0014g0039a0001c0001t0028g0022 | 3 | HG01243.hp1 HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.634+7170A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141444915 | ||||||
| chr7:141444991
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0005g0008a0001c0001t0005g0014others(3): Show | 6 | HG02258.hp2 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.634+7246G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141444991 | ||||||
| chr7:141445484
|
T | C | 30 | a0001c0001t0001g0015a0001c0001t0003g0020a0001c0001t0004g0023others(27): Show | 30 | HG00544.hp2 HG01255.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.634+7739T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141445484 | ||||||
| chr7:141446248
|
A | G | 68 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(65): Show | 68 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.634+8503A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141446248 | ||||||
| chr7:141446254
|
T | C | 68 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(65): Show | 68 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.634+8509T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141446254 | ||||||
| chr7:141446257
|
A | G | 53 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0027others(50): Show | 53 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.634+8512A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141446257 | ||||||
| chr7:141446263
|
G | T | 57 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0027others(54): Show | 57 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.634+8518G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141446263 | ||||||
| chr7:141446278
|
G | A | 1 | a0001c0002t0041g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.634+8533G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141446278 | ||||||
| chr7:141446300
|
G | A | 68 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(65): Show | 68 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.634+8555G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141446300 | ||||||
| chr7:141446346
|
C | T | 10 | a0001c0001t0002g0019a0001c0001t0008g0004a0001c0001t0025g0010others(7): Show | 10 | HG02486.hp1 HG02572.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.634+8601C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141446346 | ||||||
| chr7:141446625
|
A | G | 68 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(65): Show | 68 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.634+8880A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141446625 | ||||||
| chr7:141446719
|
C | A | 2 | a0001c0001t0035g0079a0001c0001t0044g0001 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.634+8974C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141446719 | ||||||
| chr7:141446748
|
C | G | 68 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(65): Show | 68 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.634+9003C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141446748 | ||||||
| chr7:141447124
|
C | T | 1 | a0001c0001t0005g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.634+9379C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141447124 | ||||||
| chr7:141447137
|
C | T | 64 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(61): Show | 64 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.634+9392C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141447137 | ||||||
| chr7:141447270
|
T | A | 68 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(65): Show | 68 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.634+9525T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141447270 | ||||||
| chr7:141447441
|
C | T | 11 | a0001c0001t0006g0017a0001c0001t0006g0025a0001c0001t0007g0011others(8): Show | 11 | HG01255.hp1 HG01255.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.634+9696C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141447441 | ||||||
| chr7:141447556
|
T | C | 68 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(65): Show | 68 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.634+9811T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141447556 | ||||||
| chr7:141447702
|
G | A | 1 | a0001c0002t0031g0063 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.634+9957G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141447702 | ||||||
| chr7:141447936
|
G | T | 58 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(55): Show | 58 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(55): Show |
intron_variant | MODIFIER | c.634+10191G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141447936 | ||||||
| chr7:141448342
|
T | A | 2 | a0001c0001t0035g0079a0001c0001t0044g0001 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.634+10597T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141448342 | ||||||
| chr7:141448409
|
C | G | 51 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(48): Show | 51 | HG00544.hp2 HG01106.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.634+10664C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141448409 | ||||||
| chr7:141448826
|
A | G | 6 | a0001c0001t0008g0004a0001c0001t0034g0009a0001c0001t0035g0079others(3): Show | 6 | HG02258.hp1 HG03130.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+11081A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141448826 | ||||||
| chr7:141448860
|
A | G | 1 | a0001c0003t0001g0055 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.634+11115A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141448860 | ||||||
| chr7:141448862
|
T | C | 3 | a0001c0001t0015g0028a0001c0001t0021g0077a0001c0002t0015g0056 | 3 | HG03225.hp2 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.634+11117T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141448862 | ||||||
| chr7:141449404
|
T | A | 5 | a0001c0001t0015g0028a0001c0001t0021g0077a0001c0001t0038g0034others(2): Show | 5 | HG02109.hp2 HG02922.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.634+11659T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141449404 | ||||||
| chr7:141449435
|
A | C | 1 | a0002c0006t0039g0061 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.634+11690A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141449435 | ||||||
| chr7:141449478
|
A | G | 59 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(56): Show | 59 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.634+11733A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141449478 | ||||||
| chr7:141449483
|
A | G | 2 | a0001c0001t0015g0028a0001c0002t0015g0056 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.634+11738A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141449483 | ||||||
| chr7:141449528
|
T | C | 6 | a0001c0001t0008g0004a0001c0001t0015g0028a0001c0001t0034g0009others(3): Show | 6 | HG03130.hp1 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+11783T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141449528 | ||||||
| chr7:141449546
|
G | A | 4 | a0001c0001t0015g0028a0001c0001t0021g0077a0001c0002t0015g0056others(1): Show | 4 | HG02109.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+11801G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141449546 | ||||||
| chr7:141449706
|
C | G | 15 | a0001c0001t0002g0019a0001c0001t0008g0004a0001c0001t0021g0077others(12): Show | 15 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.634+11961C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141449706 | ||||||
| chr7:141449808
|
A | G | 67 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(64): Show | 67 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(64): Show |
intron_variant | MODIFIER | c.634+12063A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141449808 | ||||||
| chr7:141450062
|
G | A | 20 | a0001c0001t0002g0019a0001c0001t0008g0004a0001c0001t0009g0078others(17): Show | 20 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.634+12317G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141450062 | ||||||
| chr7:141450384
|
C | A | 1 | a0001c0001t0011g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.634+12639C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141450384 | ||||||
| chr7:141450573
|
T | A | 1 | a0001c0002t0008g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.634+12828T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141450573 | ||||||
| chr7:141450590
|
G | T | 15 | a0001c0001t0002g0019a0001c0001t0008g0004a0001c0001t0009g0078others(12): Show | 15 | HG02486.hp1 HG02572.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.634+12845G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141450590 | ||||||
| chr7:141450622
|
C | T | 7 | a0001c0001t0005g0008a0001c0001t0005g0014a0001c0002t0005g0049others(4): Show | 7 | HG00544.hp2 HG01256.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+12877C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141450622 | ||||||
| chr7:141450914
|
G | T | 1 | a0001c0001t0033g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.634+13169G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141450914 | ||||||
| chr7:141450978
|
A | C | 1 | a0001c0001t0020g0006 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.634+13233A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141450978 | ||||||
| chr7:141451471
|
T | C | 56 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.634+13726T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141451471 | ||||||
| chr7:141451526
|
C | G | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.634+13781C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141451526 | ||||||
| chr7:141451594
|
A | G | 56 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.634+13849A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141451594 | ||||||
| chr7:141451740
|
T | A | 4 | a0001c0002t0011g0044a0001c0002t0013g0047a0001c0002t0036g0069others(1): Show | 4 | HG00544.hp2 HG01256.hp2 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+13995T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141451740 | ||||||
| chr7:141451805
|
C | G | 2 | a0001c0001t0038g0034a0001c0004t0043g0032 | 2 | HG02109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.634+14060C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141451805 | ||||||
| chr7:141451868
|
G | A | 56 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.634+14123G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141451868 | ||||||
| chr7:141451877
|
C | T | 2 | a0001c0001t0035g0079a0001c0001t0044g0001 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.634+14132C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141451877 | ||||||
| chr7:141451878
|
G | A | 1 | a0001c0002t0015g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.634+14133G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141451878 | ||||||
| chr7:141451883
|
C | G | 56 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.634+14138C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141451883 | ||||||
| chr7:141451984
|
C | T | 1 | a0001c0002t0008g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.634+14239C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141451984 | ||||||
| chr7:141452131
|
A | G | 1 | a0001c0002t0032g0071 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.634+14386A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141452131 | ||||||
| chr7:141452261
|
A | G | 2 | a0001c0001t0015g0028a0001c0002t0015g0056 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.634+14516A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141452261 | ||||||
| chr7:141452277
|
G | A | 1 | a0001c0002t0013g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.634+14532G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141452277 | ||||||
| chr7:141452299
|
C | T | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.634+14554C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141452299 | ||||||
| chr7:141452303
|
A | G | 56 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(53): Show | 56 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.634+14558A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141452303 | ||||||
| chr7:141452496
|
C | T | 7 | a0001c0001t0005g0008a0001c0001t0005g0014a0001c0002t0005g0049others(4): Show | 7 | HG00544.hp2 HG01256.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+14751C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141452496 | ||||||
| chr7:141452690
|
G | A | 46 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0027others(43): Show | 46 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.634+14945G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141452690 | ||||||
| chr7:141452736
|
A | T | 3 | a0001c0001t0035g0079a0001c0001t0044g0001a0001c0002t0040g0050 | 3 | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.634+14991A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141452736 | ||||||
| chr7:141452863
|
C | T | 58 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0027others(55): Show | 58 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.634+15118C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141452863 | ||||||
| chr7:141452864
|
A | T | 58 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0027others(55): Show | 58 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.634+15119A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141452864 | ||||||
| chr7:141452880
|
A | G | 46 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0027others(43): Show | 46 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.634+15135A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141452880 | ||||||
| chr7:141453050
|
A | G | 3 | a0001c0001t0035g0079a0001c0001t0044g0001a0001c0004t0043g0032 | 3 | HG02109.hp2 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.634+15305A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141453050 | ||||||
| chr7:141453066
|
A | T | 67 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(64): Show | 67 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(64): Show |
intron_variant | MODIFIER | c.634+15321A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141453066 | ||||||
| chr7:141453156
|
C | T | 1 | a0001c0004t0043g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.634+15411C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141453156 | ||||||
| chr7:141453185
|
G | T | 2 | a0001c0001t0035g0079a0001c0001t0044g0001 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.634+15440G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141453185 | ||||||
| chr7:141453197
|
T | C | 2 | a0001c0001t0035g0079a0001c0001t0044g0001 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.634+15452T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141453197 | ||||||
| chr7:141453409
|
A | C | 46 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0027others(43): Show | 46 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.634+15664A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141453409 | ||||||
| chr7:141453528
|
C | G | 3 | a0001c0001t0005g0008a0001c0001t0005g0014a0001c0002t0005g0049 | 3 | HG02922.hp2 HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.634+15783C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141453528 | ||||||
| chr7:141453546
|
C | A | 7 | a0001c0001t0005g0008a0001c0001t0005g0014a0001c0002t0005g0049others(4): Show | 7 | HG00544.hp2 HG01256.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+15801C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141453546 | ||||||
| chr7:141453546
|
C | T | 1 | a0001c0002t0024g0002 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.634+15801C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141453546 | ||||||
| chr7:141453705
|
C | T | 7 | a0001c0001t0002g0019a0001c0001t0009g0078a0001c0001t0010g0021others(4): Show | 7 | HG02647.hp2 HG03471.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+15960C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141453705 | ||||||
| chr7:141453776
|
C | T | 1 | a0001c0002t0008g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.634+16031C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141453776 | ||||||
| chr7:141453920
|
T | TA | 4 | a0001c0001t0015g0028a0001c0002t0015g0056a0001c0002t0026g0041others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+16186dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141453920 | |||||
| chr7:141453920
|
T | TAA | 53 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0019others(50): Show | 53 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.634+16185_634+1618 others(6): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141453920 | |||||
| chr7:141453938
|
G | A | 1 | a0001c0002t0008g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.634+16193G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141453938 | ||||||
| chr7:141453948
|
A | C | 1 | a0001c0001t0001g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.634+16203A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141453948 | ||||||
| chr7:141454316
|
C | T | 1 | a0001c0001t0020g0006 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.635-16220C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141454316 | ||||||
| chr7:141454546
|
T | TTCTCTCC others(2): Show |
7 | a0001c0002t0001g0057a0001c0003t0001g0055a0001c0003t0001g0068others(4): Show | 7 | HG01106.hp1 HG01243.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-15942_635-1593 others(13): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141454546 | |||||
| chr7:141454546
|
TTCTCTCC others(2): Show |
T | 18 | a0001c0001t0002g0019a0001c0001t0008g0004a0001c0001t0009g0078others(15): Show | 18 | HG02109.hp2 HG02486.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.635-15942_635-1593 others(13): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141454546 | |||||
| chr7:141454546
|
TTCTCTCC others(11): Show |
T | 2 | a0001c0001t0035g0079a0001c0001t0044g0001 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.635-15951_635-1593 others(22): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141454546 | |||||
| chr7:141454893
|
C | T | 17 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0002g0027others(14): Show | 17 | HG01106.hp1 HG01243.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.635-15643C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141454893 | ||||||
| chr7:141455100
|
C | A | 1 | a0001c0002t0008g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.635-15436C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141455100 | ||||||
| chr7:141455206
|
G | A | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.635-15330G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141455206 | ||||||
| chr7:141455963
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.635-14573G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141455963 | ||||||
| chr7:141456103
|
T | C | 1 | a0001c0002t0001g0057 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.635-14433T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141456103 | ||||||
| chr7:141456131
|
G | A | 2 | a0001c0001t0015g0028a0001c0002t0015g0056 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.635-14405G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141456131 | ||||||
| chr7:141456571
|
C | T | 1 | a0001c0002t0041g0058 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.635-13965C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141456571 | ||||||
| chr7:141456638
|
G | C | 1 | a0001c0001t0022g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.635-13898G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141456638 | ||||||
| chr7:141457317
|
A | C | 2 | a0001c0001t0035g0079a0001c0001t0044g0001 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.635-13219A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141457317 | ||||||
| chr7:141457348
|
C | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0080others(13): Show | 16 | HG00544.hp1 HG01106.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.635-13188C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141457348 | ||||||
| chr7:141457494
|
A | G | 6 | a0001c0001t0002g0019a0001c0001t0009g0078a0001c0001t0010g0021others(3): Show | 6 | HG02647.hp2 HG03471.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.635-13042A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141457494 | ||||||
| chr7:141457560
|
A | G | 2 | a0001c0001t0015g0028a0001c0002t0015g0056 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.635-12976A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141457560 | ||||||
| chr7:141457587
|
G | A | 1 | a0001c0002t0008g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.635-12949G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141457587 | ||||||
| chr7:141457615
|
C | T | 19 | a0001c0001t0002g0019a0001c0001t0008g0004a0001c0001t0009g0078others(16): Show | 19 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.635-12921C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141457615 | ||||||
| chr7:141457701
|
G | C | 2 | a0001c0001t0038g0034a0001c0004t0043g0032 | 2 | HG02109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.635-12835G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141457701 | ||||||
| chr7:141457938
|
A | G | 1 | a0001c0003t0018g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.635-12598A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141457938 | ||||||
| chr7:141458010
|
G | C | 1 | a0001c0001t0020g0006 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.635-12526G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141458010 | ||||||
| chr7:141458036
|
A | G | 9 | a0001c0001t0002g0019a0001c0001t0009g0078a0001c0001t0010g0021others(6): Show | 9 | HG02572.hp1 HG02647.hp2 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.635-12500A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141458036 | ||||||
| chr7:141458782
|
T | A | 13 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0080others(10): Show | 13 | HG00544.hp1 HG01106.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.635-11754T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141458782 | ||||||
| chr7:141458846
|
G | A | 2 | a0001c0001t0035g0079a0001c0001t0044g0001 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.635-11690G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141458846 | ||||||
| chr7:141458874
|
G | T | 22 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0080others(19): Show | 22 | HG00544.hp1 HG01106.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.635-11662G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141458874 | ||||||
| chr7:141458920
|
C | T | 9 | a0001c0001t0002g0019a0001c0001t0009g0078a0001c0001t0010g0021others(6): Show | 9 | HG02572.hp1 HG02647.hp2 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.635-11616C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141458920 | ||||||
| chr7:141459015
|
GGTTT | G | 12 | a0001c0001t0008g0004a0001c0001t0015g0028a0001c0001t0025g0010others(9): Show | 12 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.635-11496_635-1149 others(8): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141459015 | |||||
| chr7:141459066
|
A | G | 1 | a0001c0002t0013g0059 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.635-11470A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141459066 | ||||||
| chr7:141459068
|
T | C | 34 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0080others(31): Show | 34 | HG00544.hp1 HG01106.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.635-11468T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141459068 | ||||||
| chr7:141459080
|
T | C | 2 | a0001c0001t0015g0028a0001c0002t0015g0056 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.635-11456T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141459080 | ||||||
| chr7:141459121
|
C | T | 2 | a0001c0001t0035g0079a0001c0001t0044g0001 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.635-11415C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141459121 | ||||||
| chr7:141459319
|
C | T | 1 | a0001c0001t0025g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.635-11217C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141459319 | ||||||
| chr7:141459946
|
GA | G | 24 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0080others(21): Show | 24 | HG00544.hp1 HG01106.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.635-10574delA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141459946 | |||||
| chr7:141460039
|
G | T | 1 | a0001c0001t0008g0030 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.635-10497G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141460039 | ||||||
| chr7:141460161
|
A | G | 2 | a0001c0001t0035g0079a0001c0001t0044g0001 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.635-10375A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141460161 | ||||||
| chr7:141460282
|
C | A | 4 | a0001c0001t0008g0004a0001c0001t0034g0009a0001c0002t0040g0050others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-10254C>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141460282 | ||||||
| chr7:141460483
|
G | A | 34 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0080others(31): Show | 34 | HG00544.hp1 HG01106.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.635-10053G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141460483 | ||||||
| chr7:141460894
|
C | T | 2 | a0001c0001t0035g0079a0001c0001t0044g0001 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.635-9642C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141460894 | ||||||
| chr7:141461055
|
T | C | 29 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0080others(26): Show | 29 | HG00544.hp1 HG01106.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.635-9481T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141461055 | ||||||
| chr7:141461363
|
A | T | 34 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0080others(31): Show | 34 | HG00544.hp1 HG01106.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.635-9173A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141461363 | ||||||
| chr7:141461779
|
A | G | 2 | a0001c0001t0003g0020a0001c0001t0029g0026 | 2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.635-8757A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141461779 | ||||||
| chr7:141461811
|
G | A | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.635-8725G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141461811 | ||||||
| chr7:141461957
|
C | T | 1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.635-8579C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141461957 | ||||||
| chr7:141461959
|
G | A | 7 | a0001c0001t0008g0004a0001c0001t0011g0016a0001c0001t0034g0009others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-8577G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141461959 | ||||||
| chr7:141462157
|
T | C | 4 | a0001c0001t0014g0033a0001c0001t0014g0039a0001c0001t0028g0022others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-8379T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141462157 | ||||||
| chr7:141462300
|
G | A | 1 | a0001c0001t0010g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.635-8236G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141462300 | ||||||
| chr7:141462309
|
G | C | 1 | a0001c0002t0040g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.635-8227G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141462309 | ||||||
| chr7:141462373
|
C | T | 4 | a0001c0001t0008g0004a0001c0001t0034g0009a0001c0002t0040g0050others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-8163C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141462373 | ||||||
| chr7:141462570
|
G | A | 4 | a0001c0001t0003g0007a0001c0001t0003g0020a0001c0002t0003g0052others(1): Show | 4 | HG01891.hp2 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-7966G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141462570 | ||||||
| chr7:141462584
|
C | T | 2 | a0001c0001t0044g0001a0001c0004t0043g0032 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.635-7952C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141462584 | ||||||
| chr7:141462594
|
G | A | 2 | a0001c0001t0008g0004a0001c0001t0034g0009 | 2 | HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.635-7942G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141462594 | ||||||
| chr7:141462664
|
A | C | 11 | a0001c0001t0002g0019a0001c0001t0002g0027a0001c0001t0010g0021others(8): Show | 11 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-7872A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141462664 | ||||||
| chr7:141462779
|
A | G | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0029 | 3 | HG01952.hp2 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.635-7757A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141462779 | ||||||
| chr7:141462825
|
A | C | 10 | a0001c0001t0003g0007a0001c0001t0003g0020a0001c0001t0004g0023others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.635-7711A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141462825 | ||||||
| chr7:141463043
|
G | C | 2 | a0001c0001t0044g0001a0001c0004t0043g0032 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.635-7493G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141463043 | ||||||
| chr7:141463087
|
A | G | 24 | a0001c0001t0002g0019a0001c0001t0002g0027a0001c0001t0003g0007others(21): Show | 24 | HG01884.hp2 HG01891.hp2 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.635-7449A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141463087 | ||||||
| chr7:141463227
|
C | T | 5 | a0001c0001t0011g0016a0001c0001t0016g0037a0001c0002t0011g0044others(2): Show | 5 | HG01261.hp2 HG01891.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.635-7309C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141463227 | ||||||
| chr7:141463362
|
T | G | 1 | a0001c0002t0008g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.635-7174T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141463362 | ||||||
| chr7:141463373
|
G | A | 1 | a0001c0002t0008g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.635-7163G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141463373 | ||||||
| chr7:141463414
|
T | C | 11 | a0001c0001t0002g0019a0001c0001t0002g0027a0001c0001t0010g0021others(8): Show | 11 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.635-7122T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141463414 | ||||||
| chr7:141463445
|
A | G | 5 | a0001c0001t0002g0019a0001c0001t0002g0027a0001c0001t0010g0021others(2): Show | 5 | HG02615.hp1 HG03471.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.635-7091A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141463445 | ||||||
| chr7:141463618
|
A | T | 1 | a0001c0002t0013g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.635-6918A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141463618 | ||||||
| chr7:141463665
|
G | A | 1 | a0001c0002t0013g0047 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.635-6871G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141463665 | ||||||
| chr7:141463865
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.635-6671C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141463865 | ||||||
| chr7:141463868
|
G | A | 9 | a0001c0001t0002g0019a0001c0001t0002g0027a0001c0001t0010g0021others(6): Show | 9 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.635-6668G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141463868 | ||||||
| chr7:141464077
|
C | T | 2 | a0001c0001t0044g0001a0001c0004t0043g0032 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.635-6459C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141464077 | ||||||
| chr7:141464118
|
G | A | 6 | a0001c0003t0001g0055a0001c0003t0001g0068a0001c0003t0001g0074others(3): Show | 6 | HG01106.hp1 HG01243.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.635-6418G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141464118 | ||||||
| chr7:141464118
|
G | C | 1 | a0001c0002t0032g0071 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.635-6418G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141464118 | ||||||
| chr7:141464141
|
A | T | 1 | a0001c0001t0038g0034 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.635-6395A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141464141 | ||||||
| chr7:141464332
|
C | T | 2 | a0001c0001t0044g0001a0001c0004t0043g0032 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.635-6204C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141464332 | ||||||
| chr7:141464349
|
T | A | 15 | a0001c0001t0002g0019a0001c0001t0002g0027a0001c0001t0010g0021others(12): Show | 15 | HG02109.hp2 HG02486.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.635-6187T>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141464349 | ||||||
| chr7:141464453
|
C | T | 2 | a0001c0001t0044g0001a0001c0004t0043g0032 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.635-6083C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141464453 | ||||||
| chr7:141464650
|
A | C | 2 | a0001c0001t0015g0028a0001c0002t0015g0056 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.635-5886A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141464650 | ||||||
| chr7:141464816
|
C | T | 1 | a0001c0002t0008g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.635-5720C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141464816 | ||||||
| chr7:141464887
|
G | C | 5 | a0001c0001t0011g0016a0001c0001t0016g0037a0001c0002t0011g0044others(2): Show | 5 | HG01261.hp2 HG01891.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.635-5649G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141464887 | ||||||
| chr7:141465561
|
C | T | 9 | a0001c0001t0002g0019a0001c0001t0002g0027a0001c0001t0010g0021others(6): Show | 9 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.635-4975C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141465561 | ||||||
| chr7:141465810
|
C | G | 6 | a0001c0001t0015g0028a0001c0001t0028g0022a0001c0001t0044g0001others(3): Show | 6 | HG02109.hp2 HG03225.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.635-4726C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141465810 | ||||||
| chr7:141465874
|
T | G | 8 | a0001c0001t0003g0007a0001c0001t0003g0020a0001c0001t0004g0023others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.635-4662T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141465874 | ||||||
| chr7:141465890
|
G | A | 1 | a0001c0001t0035g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.635-4646G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141465890 | ||||||
| chr7:141466044
|
A | G | 10 | a0001c0001t0003g0007a0001c0001t0003g0020a0001c0001t0014g0033others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.635-4492A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141466044 | ||||||
| chr7:141466308
|
A | G | 2 | a0001c0001t0044g0001a0001c0004t0043g0032 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.635-4228A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141466308 | ||||||
| chr7:141466365
|
G | A | 4 | a0001c0001t0003g0007a0001c0001t0003g0020a0001c0001t0029g0026others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-4171G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141466365 | ||||||
| chr7:141466526
|
C | T | 1 | a0001c0001t0028g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.635-4010C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141466526 | ||||||
| chr7:141467355
|
C | T | 2 | a0001c0001t0009g0078a0001c0002t0009g0060 | 2 | HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.635-3181C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141467355 | ||||||
| chr7:141467643
|
G | A | 23 | a0001c0001t0002g0019a0001c0001t0002g0027a0001c0001t0003g0007others(20): Show | 23 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.635-2893G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141467643 | ||||||
| chr7:141467856
|
G | C | 5 | a0001c0001t0001g0015a0001c0001t0022g0013a0001c0002t0001g0042others(2): Show | 5 | HG01261.hp1 HG02258.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.635-2680G>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141467856 | ||||||
| chr7:141467915
|
G | T | 6 | a0001c0001t0003g0007a0001c0001t0003g0020a0001c0001t0029g0026others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.635-2621G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141467915 | ||||||
| chr7:141467971
|
C | CA | 11 | a0001c0001t0004g0023a0001c0001t0004g0029a0001c0001t0011g0016others(8): Show | 11 | HG01261.hp2 HG01891.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.635-2548dupA | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141467971 | |||||
| chr7:141467971
|
C | CAA | 4 | a0001c0001t0003g0007a0001c0001t0003g0020a0001c0001t0029g0026others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-2549_635-2548d others(4): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141467971 | |||||
| chr7:141467975
|
A | C | 6 | a0001c0001t0015g0028a0001c0001t0028g0022a0001c0001t0044g0001others(3): Show | 6 | HG02109.hp2 HG03225.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.635-2561A>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141467975 | ||||||
| chr7:141468010
|
A | G | 2 | a0001c0001t0015g0028a0001c0002t0015g0056 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.635-2526A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141468010 | ||||||
| chr7:141468056
|
C | G | 2 | a0001c0001t0035g0079a0001c0001t0038g0034 | 2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.635-2480C>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141468056 | ||||||
| chr7:141468098
|
A | G | 9 | a0001c0001t0003g0007a0001c0001t0003g0020a0001c0001t0004g0023others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.635-2438A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141468098 | ||||||
| chr7:141468184
|
A | G | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0029 | 3 | HG01952.hp2 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.635-2352A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141468184 | ||||||
| chr7:141468203
|
A | G | 26 | a0001c0001t0002g0019a0001c0001t0002g0027a0001c0001t0003g0007others(23): Show | 26 | HG01884.hp2 HG01891.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.635-2333A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141468203 | ||||||
| chr7:141468229
|
C | T | 9 | a0001c0001t0002g0019a0001c0001t0002g0027a0001c0001t0010g0021others(6): Show | 9 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.635-2307C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141468229 | ||||||
| chr7:141468571
|
A | G | 1 | a0001c0001t0009g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.635-1965A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141468571 | ||||||
| chr7:141468620
|
G | A | 1 | a0001c0002t0008g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.635-1916G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141468620 | ||||||
| chr7:141468687
|
A | G | 2 | a0001c0001t0009g0078a0001c0002t0009g0060 | 2 | HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.635-1849A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141468687 | ||||||
| chr7:141468750
|
A | G | 9 | a0001c0001t0002g0019a0001c0001t0002g0027a0001c0001t0010g0021others(6): Show | 9 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.635-1786A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141468750 | ||||||
| chr7:141468872
|
C | T | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0029 | 3 | HG01952.hp2 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.635-1664C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141468872 | ||||||
| chr7:141469319
|
T | G | 1 | a0001c0001t0020g0006 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.635-1217T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141469319 | ||||||
| chr7:141469323
|
T | G | 4 | a0001c0001t0028g0022a0001c0001t0044g0001a0001c0004t0043g0032others(1): Show | 4 | HG02109.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-1213T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141469323 | ||||||
| chr7:141469382
|
C | T | 2 | a0001c0002t0011g0044a0001c0002t0037g0075 | 2 | HG02027.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.635-1154C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141469382 | ||||||
| chr7:141469560
|
T | G | 5 | a0001c0001t0028g0022a0001c0001t0044g0001a0001c0002t0008g0003others(2): Show | 5 | HG02109.hp2 HG03225.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.635-976T>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141469560 | ||||||
| chr7:141469667
|
A | G | 4 | a0001c0001t0028g0022a0001c0001t0044g0001a0001c0004t0043g0032others(1): Show | 4 | HG02109.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-869A>G | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141469667 | ||||||
| chr7:141469674
|
AT | A | 2 | a0001c0001t0016g0037a0001c0002t0016g0072 | 2 | HG01261.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.635-860delT | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141469674 | |||||
| chr7:141469706
|
T | C | 4 | a0001c0001t0028g0022a0001c0001t0044g0001a0001c0004t0043g0032others(1): Show | 4 | HG02109.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-830T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141469706 | ||||||
| chr7:141469848
|
AAAGTAGG others(2): Show |
A | 9 | a0001c0001t0002g0019a0001c0001t0002g0027a0001c0001t0010g0021others(6): Show | 9 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.635-686_635-678del others(9): Show |
TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 141469848 | |||||
| chr7:141469859
|
G | T | 1 | a0001c0001t0035g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.635-677G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141469859 | ||||||
| chr7:141469862
|
G | A | 1 | a0001c0001t0035g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.635-674G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141469862 | ||||||
| chr7:141469865
|
T | C | 1 | a0001c0001t0035g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.635-671T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141469865 | ||||||
| chr7:141469866
|
T | C | 1 | a0001c0001t0035g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.635-670T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141469866 | ||||||
| chr7:141469880
|
C | T | 4 | a0001c0001t0016g0037a0001c0001t0044g0001a0001c0002t0016g0072others(1): Show | 4 | HG01261.hp2 HG01891.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-656C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141469880 | ||||||
| chr7:141469881
|
G | A | 1 | a0001c0002t0002g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.635-655G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141469881 | ||||||
| chr7:141469927
|
C | T | 1 | a0001c0001t0028g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.635-609C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141469927 | ||||||
| chr7:141469941
|
G | T | 1 | a0001c0002t0042g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.635-595G>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141469941 | ||||||
| chr7:141469977
|
C | T | 57 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0035others(54): Show | 57 | HG00544.hp1 HG01106.hp1 HG01106.hp2 others(54): Show |
intron_variant | MODIFIER | c.635-559C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141469977 | ||||||
| chr7:141470243
|
T | C | 2 | a0001c0001t0015g0028a0001c0002t0015g0056 | 2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.635-293T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141470243 | ||||||
| chr7:141470249
|
T | C | 6 | a0001c0001t0016g0037a0001c0001t0028g0022a0001c0001t0044g0001others(3): Show | 6 | HG01261.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.635-287T>C | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141470249 | ||||||
| chr7:141470321
|
A | T | 1 | a0001c0001t0028g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.635-215A>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141470321 | ||||||
| chr7:141470378
|
C | T | 6 | a0001c0001t0016g0037a0001c0001t0028g0022a0001c0001t0044g0001others(3): Show | 6 | HG01261.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.635-158C>T | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141470378 | ||||||
| chr7:141470477
|
G | A | 1 | a0001c0002t0002g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.635-59G>A | TMEM178B | ENSG00000261115.7 | transcript | ENST00000565468.6 | protein_coding | 3/3 | chr7 | 141470477 |