| geneid | 84498 |
|---|---|
| ensemblid | ENSG00000112584.14 |
| hgncid | 21109 |
| symbol | FAM120B |
| name | family with sequence similarity 120B |
| refseq_nuc | NM_032448.3 |
| refseq_prot | NP_115824.1 |
| ensembl_nuc | ENST00000476287.4 |
| ensembl_prot | ENSP00000417970.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 170306758 |
| end | 170407067 |
| strand | + |
| ver | v1.2 |
| region | chr6:170306758-170407067 |
| region5000 | chr6:170301758-170412067 |
| regionname0 | FAM120B_chr6_170306758_170407067 |
| regionname5000 | FAM120B_chr6_170301758_170412067 |
| 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 | 0/1 | 910 | 203 | 65 | 55 | 46 | 7 | 29 | 35 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0002 | 0/0 | 922 | 46 | 3 | 10 | 27 | 1 | 5 | 23 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0003 | 0/0 | 922 | 22 | 0 | 6 | 16 | 0 | 0 | 13 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0004 | 0/0 | 910 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0005 | 0/0 | 910 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0006 | 0/0 | 910 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0007 | 0/0 | 910 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0008 | 0/0 | 910 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0009 | 0/0 | 910 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0010 | 0/0 | 910 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0011 | 0/0 | 922 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| 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 | 0/1 | 2733 | 99 | 32 | 35 | 8 | 5 | 18 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| c0002 | 0/0 | 2733 | 93 | 28 | 19 | 33 | 2 | 11 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| c0003 | 0/0 | 2769 | 46 | 3 | 10 | 27 | 1 | 5 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| c0004 | 0/0 | 2769 | 22 | 0 | 6 | 16 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| c0005 | 0/0 | 2733 | 7 | 7 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| c0006 | 0/0 | 2733 | 4 | 1 | 0 | 3 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| c0007 | 0/0 | 2733 | 4 | 4 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| c0008 | 0/0 | 2733 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| c0009 | 0/0 | 2733 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| c0010 | 0/0 | 2733 | 2 | 1 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| c0011 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| c0012 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| c0013 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| c0014 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| c0015 | 0/0 | 2733 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| c0016 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| c0017 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| c0018 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| 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 | 2423 | 119 | 48 | 19 | 39 | 1 | 12 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0002 | 0/0 | 2423 | 41 | 1 | 10 | 24 | 1 | 5 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0003 | 0/0 | 2423 | 20 | 0 | 4 | 16 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0004 | 0/0 | 2423 | 15 | 2 | 7 | 1 | 1 | 4 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0005 | 0/0 | 2422 | 15 | 2 | 10 | 0 | 2 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0006 | 0/1 | 2422 | 14 | 0 | 6 | 1 | 0 | 6 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0007 | 0/0 | 2423 | 13 | 2 | 7 | 0 | 1 | 3 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0008 | 0/0 | 2423 | 9 | 0 | 0 | 9 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0009 | 0/0 | 2423 | 9 | 8 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0010 | 0/0 | 2423 | 6 | 5 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0011 | 0/0 | 2423 | 3 | 3 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0012 | 0/0 | 2423 | 3 | 3 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0013 | 0/0 | 2423 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0014 | 0/0 | 2422 | 2 | 0 | 0 | 0 | 1 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0015 | 0/0 | 2423 | 2 | 0 | 2 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0016 | 0/0 | 2423 | 2 | 0 | 2 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0017 | 0/0 | 2411 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0018 | 0/0 | 2411 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0019 | 0/0 | 2423 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0020 | 0/0 | 2422 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0021 | 0/0 | 2423 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0022 | 0/0 | 2423 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0023 | 0/0 | 2423 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0024 | 0/0 | 2423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0025 | 0/0 | 2423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0026 | 0/0 | 2422 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0027 | 0/0 | 2422 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0028 | 0/0 | 2423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0029 | 0/0 | 2423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| t0030 | 0/0 | 2423 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| 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 | 2 | 0 | 0 | 2 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0216 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| 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 | 0/1 | 2733 | 99 | 32 | 35 | 8 | 5 | 18 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0002 | 0/0 | 2733 | 93 | 28 | 19 | 33 | 2 | 11 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0006 | 0/0 | 2733 | 4 | 1 | 0 | 3 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0008 | 0/0 | 2733 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0009 | 0/0 | 2733 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0015 | 0/0 | 2733 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0017 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0018 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0002c0003 | 0/0 | 2769 | 46 | 3 | 10 | 27 | 1 | 5 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0003c0004 | 0/0 | 2769 | 22 | 0 | 6 | 16 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0004c0005 | 0/0 | 2733 | 7 | 7 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0005c0007 | 0/0 | 2733 | 4 | 4 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0006c0010 | 0/0 | 2733 | 2 | 1 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0007c0012 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0008c0016 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0009c0014 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0010c0013 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0011c0011 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5155 | 43 | 20 | 13 | 0 | 1 | 9 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0001t0002 | 0/0 | 5155 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0001t0005 | 0/0 | 5154 | 15 | 2 | 10 | 0 | 2 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0001t0006 | 0/1 | 5154 | 13 | 0 | 6 | 0 | 0 | 6 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0001t0008 | 0/0 | 5155 | 8 | 0 | 0 | 8 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0001t0009 | 0/0 | 5155 | 7 | 6 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0001t0010 | 0/0 | 5155 | 3 | 3 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0001t0014 | 0/0 | 5154 | 2 | 0 | 0 | 0 | 1 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0001t0016 | 0/0 | 5155 | 2 | 0 | 2 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0001t0019 | 0/0 | 5155 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0001t0020 | 0/0 | 5154 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0001t0025 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0001t0026 | 0/0 | 5154 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0001t0027 | 0/0 | 5154 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0002t0001 | 0/0 | 5155 | 58 | 18 | 5 | 32 | 0 | 3 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0002t0004 | 0/0 | 5155 | 15 | 2 | 7 | 1 | 1 | 4 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0002t0007 | 0/0 | 5155 | 11 | 0 | 7 | 0 | 1 | 3 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0002t0010 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0002t0011 | 0/0 | 5155 | 3 | 3 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0002t0013 | 0/0 | 5155 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0002t0024 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0002t0029 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0002t0030 | 0/0 | 5155 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0006t0001 | 0/0 | 5155 | 4 | 1 | 0 | 3 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0008t0001 | 0/0 | 5155 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0009t0017 | 0/0 | 5143 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0009t0018 | 0/0 | 5143 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0015t0001 | 0/0 | 5155 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0017t0001 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0001c0018t0006 | 0/0 | 5154 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0002c0003t0001 | 0/0 | 5191 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0002c0003t0002 | 0/0 | 5191 | 40 | 1 | 9 | 24 | 1 | 5 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0002c0003t0007 | 0/0 | 5191 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0002c0003t0021 | 0/0 | 5191 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0002c0003t0022 | 0/0 | 5191 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0002c0003t0023 | 0/0 | 5191 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0003c0004t0003 | 0/0 | 5191 | 20 | 0 | 4 | 16 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0003c0004t0015 | 0/0 | 5191 | 2 | 0 | 2 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0004c0005t0001 | 0/0 | 5155 | 6 | 6 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0004c0005t0009 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0005c0007t0012 | 0/0 | 5155 | 3 | 3 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0005c0007t0028 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0006c0010t0010 | 0/0 | 5155 | 2 | 1 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0007c0012t0001 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0008c0016t0008 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0009c0014t0009 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0010c0013t0001 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| a0011c0011t0001 | 0/0 | 5191 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | copy fasta | chr6 | 170301758 | 170412067 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0005g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0006g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0006g0216 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0006g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0008g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0008g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0008g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0008g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0008g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0008g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0008g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0009g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0009g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0009g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0009g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0009g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0009g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0010g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0010g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0010g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0014g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0014g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0016g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0016g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0019g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0020g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0025g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0026g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0001t0027g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0004g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0004g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0007g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0007g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0007g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0007g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0007g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0007g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0007g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0007g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0010g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0011g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0011g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0011g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0013g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0013g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0024g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0029g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0002t0030g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0006t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0006t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0006t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0006t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0008t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0008t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0009t0017g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0009t0018g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0015t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0017t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0001c0018t0006g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0021g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0022g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0002c0003t0023g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0015g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0003c0004t0015g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0004c0005t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0004c0005t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0004c0005t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0004c0005t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0004c0005t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0004c0005t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0004c0005t0009g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0005c0007t0012g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0005c0007t0012g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0005c0007t0028g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0006c0010t0010g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0006c0010t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0007c0012t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0008c0016t0008g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0009c0014t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0010c0013t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| a0011c0011t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0004 | g0033 | EUR | GBR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00099 | hp2 | a0002 | c0003 | t0002 | g0004 | EUR | GBR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00280 | hp1 | a0001 | c0002 | t0007 | g0185 | EUR | FIN | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | FIN | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0263 | EUR | FIN | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00323 | hp2 | a0001 | c0001 | t0014 | g0212 | EUR | FIN | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00558 | hp1 | a0007 | c0012 | t0001 | g0052 | EAS | CHS | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00558 | hp2 | a0002 | c0003 | t0002 | g0123 | EAS | CHS | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0214 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00642 | hp1 | a0001 | c0002 | t0004 | g0180 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0209 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | CHS | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00673 | hp2 | a0002 | c0003 | t0002 | g0135 | EAS | CHS | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00733 | hp1 | a0001 | c0001 | t0027 | g0210 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00733 | hp2 | a0001 | c0002 | t0007 | g0183 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00735 | hp1 | a0003 | c0004 | t0003 | g0154 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0225 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00738 | hp2 | a0001 | c0002 | t0004 | g0028 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01069 | hp1 | a0003 | c0004 | t0015 | g0155 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01070 | hp1 | a0001 | c0002 | t0007 | g0006 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01070 | hp2 | a0002 | c0003 | t0002 | g0139 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01071 | hp1 | a0003 | c0004 | t0015 | g0151 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01071 | hp2 | a0001 | c0002 | t0007 | g0006 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01081 | hp1 | a0001 | c0002 | t0004 | g0029 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01081 | hp2 | a0001 | c0002 | t0007 | g0186 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01099 | hp1 | a0006 | c0010 | t0010 | g0019 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01099 | hp2 | a0001 | c0002 | t0004 | g0179 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01106 | hp1 | a0001 | c0002 | t0004 | g0023 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0213 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0009 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01167 | hp1 | a0001 | c0002 | t0004 | g0026 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0171 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01175 | hp2 | a0001 | c0002 | t0004 | g0178 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01192 | hp1 | a0001 | c0015 | t0001 | g0252 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0205 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01243 | hp2 | a0001 | c0001 | t0016 | g0199 | AMR | PUR | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01255 | hp2 | a0002 | c0003 | t0002 | g0131 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01256 | hp1 | a0002 | c0003 | t0002 | g0128 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01256 | hp2 | a0001 | c0002 | t0007 | g0007 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01257 | hp1 | a0001 | c0002 | t0007 | g0184 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0217 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01258 | hp1 | a0001 | c0002 | t0007 | g0007 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0218 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01261 | hp1 | a0002 | c0003 | t0002 | g0141 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0221 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01361 | hp1 | a0002 | c0003 | t0002 | g0132 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0175 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01433 | hp1 | a0002 | c0003 | t0002 | g0136 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01433 | hp2 | a0003 | c0004 | t0003 | g0152 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0172 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01891 | hp2 | a0001 | c0002 | t0013 | g0039 | AFR | ACB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01934 | hp2 | a0001 | c0001 | t0020 | g0206 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01943 | hp1 | a0002 | c0003 | t0002 | g0109 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0219 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0176 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01978 | hp2 | a0003 | c0004 | t0003 | g0163 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0078 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0177 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01993 | hp2 | a0002 | c0003 | t0002 | g0143 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0224 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02004 | hp2 | a0002 | c0003 | t0022 | g0144 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02015 | hp1 | a0001 | c0001 | t0008 | g0271 | EAS | KHV | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | KHV | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02055 | hp1 | a0005 | c0007 | t0012 | g0002 | AFR | ACB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02055 | hp2 | a0001 | c0002 | t0004 | g0104 | AFR | ACB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02056 | hp1 | a0003 | c0004 | t0003 | g0160 | EAS | KHV | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | KHV | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02129 | hp1 | a0001 | c0001 | t0008 | g0200 | EAS | KHV | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | KHV | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02132 | hp1 | a0001 | c0002 | t0004 | g0022 | EAS | KHV | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02132 | hp2 | a0003 | c0004 | t0003 | g0161 | EAS | KHV | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0202 | AFR | ACB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | ACB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02155 | hp1 | a0002 | c0003 | t0002 | g0133 | EAS | CDX | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02155 | hp2 | a0008 | c0016 | t0008 | g0196 | EAS | CDX | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02258 | hp2 | a0001 | c0001 | t0009 | g0191 | AFR | ACB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02293 | hp1 | a0001 | c0001 | t0006 | g0173 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02300 | hp1 | a0003 | c0004 | t0003 | g0153 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PEL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02451 | hp1 | a0005 | c0007 | t0028 | g0003 | AFR | ACB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | ACB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | KHV | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02523 | hp2 | a0003 | c0004 | t0003 | g0159 | EAS | KHV | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0009 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02602 | hp1 | a0001 | c0002 | t0004 | g0034 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02602 | hp2 | a0001 | c0001 | t0026 | g0223 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02615 | hp1 | a0001 | c0002 | t0011 | g0017 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02647 | hp1 | a0001 | c0002 | t0013 | g0040 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02717 | hp1 | a0001 | c0001 | t0010 | g0095 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02723 | hp2 | a0004 | c0005 | t0009 | g0090 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0256 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02809 | hp1 | a0001 | c0002 | t0010 | g0103 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02818 | hp1 | a0001 | c0002 | t0011 | g0016 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02886 | hp1 | a0001 | c0008 | t0001 | g0099 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0101 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0189 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02895 | hp2 | a0002 | c0003 | t0007 | g0145 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02896 | hp2 | a0002 | c0003 | t0007 | g0112 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0043 | AFR | ESN | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02965 | hp2 | a0004 | c0005 | t0001 | g0086 | AFR | ESN | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02970 | hp1 | a0006 | c0010 | t0010 | g0020 | AFR | ESN | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | ESN | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02976 | hp2 | a0001 | c0002 | t0011 | g0018 | AFR | ESN | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03017 | hp1 | a0001 | c0002 | t0004 | g0025 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03041 | hp1 | a0001 | c0002 | t0024 | g0030 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03041 | hp2 | a0004 | c0005 | t0001 | g0087 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03098 | hp1 | a0009 | c0014 | t0009 | g0193 | AFR | MSL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03098 | hp2 | a0004 | c0005 | t0001 | g0084 | AFR | MSL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | ESN | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03139 | hp1 | a0001 | c0002 | t0029 | g0091 | AFR | ESN | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | ESN | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03209 | hp1 | a0001 | c0001 | t0025 | g0187 | AFR | MSL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03209 | hp2 | a0001 | c0009 | t0018 | g0092 | AFR | MSL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03225 | hp1 | a0010 | c0013 | t0001 | g0237 | AFR | MSL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03225 | hp2 | a0005 | c0007 | t0012 | g0002 | AFR | MSL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | MSL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0278 | AFR | MSL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03486 | hp1 | a0001 | c0009 | t0017 | g0093 | AFR | MSL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03486 | hp2 | a0004 | c0005 | t0001 | g0089 | AFR | MSL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0203 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03490 | hp2 | a0001 | c0002 | t0007 | g0008 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03492 | hp1 | a0001 | c0002 | t0007 | g0008 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03492 | hp2 | a0001 | c0002 | t0004 | g0069 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03516 | hp1 | a0004 | c0005 | t0001 | g0085 | AFR | ESN | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | ESN | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | MSL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03579 | hp2 | a0005 | c0007 | t0012 | g0003 | AFR | MSL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0222 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03669 | hp2 | a0002 | c0003 | t0002 | g0130 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0201 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03710 | hp2 | a0002 | c0003 | t0002 | g0004 | SAS | PJL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0064 | SAS | BEB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03834 | hp1 | a0001 | c0001 | t0006 | g0174 | SAS | BEB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0059 | SAS | BEB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0060 | SAS | BEB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0208 | SAS | BEB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03942 | hp1 | a0002 | c0003 | t0002 | g0127 | SAS | BEB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG04115 | hp1 | a0001 | c0002 | t0004 | g0072 | SAS | STU | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG04115 | hp2 | a0002 | c0003 | t0002 | g0116 | SAS | STU | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG04184 | hp1 | a0002 | c0003 | t0002 | g0110 | SAS | BEB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG04204 | hp1 | a0001 | c0002 | t0007 | g0181 | SAS | STU | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0220 | SAS | STU | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | YRI | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0096 | AFR | YRI | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | CHB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18612 | hp2 | a0002 | c0003 | t0002 | g0122 | EAS | CHB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18747 | hp1 | a0001 | c0001 | t0008 | g0192 | EAS | CHB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18747 | hp2 | a0001 | c0017 | t0001 | g0080 | EAS | CHB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18906 | hp1 | a0004 | c0005 | t0001 | g0088 | AFR | YRI | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | YRI | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18939 | hp1 | a0001 | c0001 | t0008 | g0197 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18942 | hp1 | a0003 | c0004 | t0003 | g0005 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18944 | hp1 | a0003 | c0004 | t0003 | g0168 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18945 | hp1 | a0002 | c0003 | t0002 | g0118 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18945 | hp2 | a0003 | c0004 | t0003 | g0005 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18947 | hp2 | a0002 | c0003 | t0002 | g0146 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18949 | hp2 | a0001 | c0006 | t0001 | g0246 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18952 | hp1 | a0001 | c0001 | t0008 | g0010 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18959 | hp1 | a0003 | c0004 | t0003 | g0164 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18959 | hp2 | a0001 | c0018 | t0006 | g0215 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18964 | hp2 | a0002 | c0003 | t0002 | g0117 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18968 | hp1 | a0001 | c0006 | t0001 | g0253 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18968 | hp2 | a0002 | c0003 | t0002 | g0137 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18969 | hp1 | a0003 | c0004 | t0003 | g0162 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18969 | hp2 | a0002 | c0003 | t0002 | g0107 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18970 | hp1 | a0003 | c0004 | t0003 | g0158 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18971 | hp1 | a0001 | c0001 | t0008 | g0194 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18974 | hp2 | a0011 | c0011 | t0001 | g0129 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18975 | hp1 | a0002 | c0003 | t0002 | g0150 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18978 | hp1 | a0002 | c0003 | t0002 | g0106 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18979 | hp1 | a0001 | c0001 | t0008 | g0195 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18979 | hp2 | a0003 | c0004 | t0003 | g0167 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18982 | hp1 | a0003 | c0004 | t0003 | g0165 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18982 | hp2 | a0002 | c0003 | t0002 | g0114 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18983 | hp1 | a0002 | c0003 | t0002 | g0121 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18990 | hp1 | a0003 | c0004 | t0003 | g0170 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18990 | hp2 | a0002 | c0003 | t0002 | g0115 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18998 | hp1 | a0002 | c0003 | t0002 | g0148 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19001 | hp2 | a0002 | c0003 | t0021 | g0113 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19009 | hp2 | a0002 | c0003 | t0023 | g0138 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19030 | hp1 | a0001 | c0008 | t0001 | g0098 | AFR | LWK | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | LWK | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0083 | AFR | LWK | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0249 | AFR | LWK | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19060 | hp2 | a0003 | c0004 | t0003 | g0156 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19065 | hp1 | a0002 | c0003 | t0002 | g0111 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19065 | hp2 | a0002 | c0003 | t0002 | g0149 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19066 | hp1 | a0003 | c0004 | t0003 | g0169 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19066 | hp2 | a0002 | c0003 | t0001 | g0134 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19068 | hp2 | a0002 | c0003 | t0002 | g0126 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19074 | hp2 | a0002 | c0003 | t0002 | g0124 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19076 | hp1 | a0003 | c0004 | t0003 | g0157 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19079 | hp1 | a0002 | c0003 | t0002 | g0125 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19081 | hp1 | a0002 | c0003 | t0002 | g0140 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19081 | hp2 | a0001 | c0001 | t0008 | g0010 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19084 | hp2 | a0002 | c0003 | t0002 | g0119 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19085 | hp1 | a0001 | c0006 | t0001 | g0254 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19089 | hp1 | a0003 | c0004 | t0003 | g0166 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19090 | hp1 | a0002 | c0003 | t0002 | g0108 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | YRI | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | YRI | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ASW | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA20129 | hp2 | a0002 | c0003 | t0002 | g0147 | AFR | ASW | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA20752 | hp1 | a0001 | c0001 | t0019 | g0211 | EUR | TSI | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0258 | EUR | TSI | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA20905 | hp1 | a0001 | c0002 | t0030 | g0182 | SAS | GIH | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA20905 | hp2 | a0001 | c0001 | t0014 | g0226 | SAS | GIH | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01123 | hp1 | a0001 | c0001 | t0016 | g0198 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG01123 | hp2 | a0002 | c0003 | t0002 | g0142 | AMR | CLM | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0027 | AFR | ACB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0188 | AFR | ACB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | ACB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0190 | AFR | ACB | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | USA | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18955 | hp1 | a0002 | c0003 | t0002 | g0120 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA20300 | hp1 | a0001 | c0006 | t0001 | g0255 | AFR | USA | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | USA | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0006 | g0216 | REF | REF | FAM120B_chr6_170301758_170412067 | FAM120B | chr6 | 170301758 | 170412067 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:170318216
|
T | C | 1 | a0007 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.826T>C | p.Tyr276His | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 932/5155 | 826/2733 | 276/910 | chr6 | 170318216 | ||
| chr6:170318498
|
G | T | 3 | a0002a0005a0011 | 51 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(48): Show |
missense_variant | MODERATE | c.1108G>T | p.Asp370Tyr | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 1214/5155 | 1108/2733 | 370/910 | chr6 | 170318498 | ||
| chr6:170318526
|
T | C | 4 | a0002a0003a0005others(1): Show | 73 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(70): Show |
missense_variant | MODERATE | c.1136T>C | p.Met379Thr | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 1242/5155 | 1136/2733 | 379/910 | chr6 | 170318526 | ||
| chr6:170318568
|
C | G | 1 | a0011 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.1178C>G | p.Thr393Arg | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 1284/5155 | 1178/2733 | 393/910 | chr6 | 170318568 | ||
| chr6:170318607
|
A | ACCCTGAA others(29): Show |
3 | a0002a0003a0011 | 69 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
conservative_inframe_insertion | MODERATE | c.1225_1260dupCCCAGG others(30): Show |
p.Pro409_Glu420dup | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 1367/5155 | 1261/2733 | 421/910 | INFO_REALIGN_3_PRIME | chr6 | 170318607 | |
| chr6:170318651
|
G | C | 1 | a0005 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
missense_variant | MODERATE | c.1261G>C | p.Ala421Pro | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 1367/5155 | 1261/2733 | 421/910 | chr6 | 170318651 | ||
| chr6:170318673
|
A | G | 5 | a0002a0003a0005others(2): Show | 75 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(72): Show |
missense_variant | MODERATE | c.1283A>G | p.Tyr428Cys | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 1389/5155 | 1283/2733 | 428/910 | chr6 | 170318673 | ||
| chr6:170318679
|
A | G | 1 | a0005 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
missense_variant | MODERATE | c.1289A>G | p.Asp430Gly | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 1395/5155 | 1289/2733 | 430/910 | chr6 | 170318679 | ||
| chr6:170318681
|
T | C | 1 | a0005 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
missense_variant | MODERATE | c.1291T>C | p.Ser431Pro | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 1397/5155 | 1291/2733 | 431/910 | chr6 | 170318681 | ||
| chr6:170318687
|
C | G | 1 | a0005 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
missense_variant | MODERATE | c.1297C>G | p.Pro433Ala | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 1403/5155 | 1297/2733 | 433/910 | chr6 | 170318687 | ||
| chr6:170318709
|
A | G | 3 | a0002a0005a0011 | 51 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(48): Show |
missense_variant | MODERATE | c.1319A>G | p.Tyr440Cys | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 1425/5155 | 1319/2733 | 440/910 | chr6 | 170318709 | ||
| chr6:170318715
|
A | G | 1 | a0004 | 7 | HG02723.hp2 HG02965.hp2 HG03041.hp2 others(4): Show |
missense_variant | MODERATE | c.1325A>G | p.Asp442Gly | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 1431/5155 | 1325/2733 | 442/910 | chr6 | 170318715 | ||
| chr6:170318745
|
A | G | 1 | a0005 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
missense_variant | MODERATE | c.1355A>G | p.Tyr452Cys | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 1461/5155 | 1355/2733 | 452/910 | chr6 | 170318745 | ||
| chr6:170318751
|
G | A | 1 | a0005 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
missense_variant | MODERATE | c.1361G>A | p.Gly454Asp | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 1467/5155 | 1361/2733 | 454/910 | chr6 | 170318751 | ||
| chr6:170318921
|
T | G | 4 | a0002a0003a0005others(1): Show | 73 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(70): Show |
missense_variant | MODERATE | c.1531T>G | p.Cys511Gly | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 1637/5155 | 1531/2733 | 511/910 | chr6 | 170318921 | ||
| chr6:170348265
|
A | T | 1 | a0008 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.2132A>T | p.Gln711Leu | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/11 | 2238/5155 | 2132/2733 | 711/910 | chr6 | 170348265 | ||
| chr6:170388390
|
C | T | 1 | a0009 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.2387C>T | p.Thr796Met | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/11 | 2493/5155 | 2387/2733 | 796/910 | chr6 | 170388390 | ||
| chr6:170391019
|
C | T | 1 | a0010 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.2497C>T | p.Arg833Trp | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/11 | 2603/5155 | 2497/2733 | 833/910 | chr6 | 170391019 | ||
| chr6:170391095
|
G | A | 1 | a0008 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.2573G>A | p.Arg858Gln | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/11 | 2679/5155 | 2573/2733 | 858/910 | chr6 | 170391095 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:170317474
|
G | A | 1 | a0001c0006 | 4 | NA18949.hp2 NA18968.hp1 NA19085.hp1 others(1): Show |
synonymous_variant | LOW | c.84G>A | p.Glu28Glu | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 190/5155 | 84/2733 | 28/910 | chr6 | 170317474 | ||
| chr6:170317855
|
T | C | 4 | a0002c0003a0003c0004a0005c0007others(1): Show | 73 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(70): Show |
synonymous_variant | LOW | c.465T>C | p.Ser155Ser | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 571/5155 | 465/2733 | 155/910 | chr6 | 170317855 | ||
| chr6:170318086
|
C | T | 1 | a0001c0018 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.696C>T | p.Asp232Asp | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 802/5155 | 696/2733 | 232/910 | chr6 | 170318086 | ||
| chr6:170318134
|
G | A | 1 | a0001c0008 | 2 | HG02886.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.744G>A | p.Ser248Ser | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 850/5155 | 744/2733 | 248/910 | chr6 | 170318134 | ||
| chr6:170318563
|
G | A | 8 | a0001c0001a0001c0006a0001c0015others(5): Show | 115 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
synonymous_variant | LOW | c.1173G>A | p.Thr391Thr | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 1279/5155 | 1173/2733 | 391/910 | chr6 | 170318563 | ||
| chr6:170318749
|
A | G | 1 | a0001c0009 | 2 | HG03209.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.1359A>G | p.Thr453Thr | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/11 | 1465/5155 | 1359/2733 | 453/910 | chr6 | 170318749 | ||
| chr6:170358231
|
C | T | 1 | a0001c0015 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.2196C>T | p.Asp732Asp | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/11 | 2302/5155 | 2196/2733 | 732/910 | chr6 | 170358231 | ||
| chr6:170388445
|
C | T | 1 | a0001c0017 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.2442C>T | p.Tyr814Tyr | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/11 | 2548/5155 | 2442/2733 | 814/910 | chr6 | 170388445 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:170306769
|
C | T | 1 | a0001c0002t0030 | 1 | NA20905.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-95C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/11 | chr6 | 170306769 | ||||||
| chr6:170306772
|
TGGCGGTG others(5): Show |
T | 2 | a0001c0009t0017a0001c0009t0018 | 2 | HG03209.hp2 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-86_-75delTGGCTGAG others(4): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/11 | 10602 | INFO_REALIGN_3_PRIME | chr6 | 170306772 | ||||
| chr6:170306801
|
G | C | 1 | a0001c0002t0013 | 2 | HG01891.hp2 HG02647.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/11 | chr6 | 170306801 | ||||||
| chr6:170306811
|
C | T | 1 | a0001c0002t0029 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-53C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/11 | 10580 | chr6 | 170306811 | |||||
| chr6:170306813
|
C | A | 1 | a0001c0001t0014 | 2 | HG00323.hp2 NA20905.hp2 |
5_prime_UTR_variant | MODIFIER | c.-51C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/11 | 10578 | chr6 | 170306813 | |||||
| chr6:170306820
|
G | A | 2 | a0001c0001t0019a0001c0001t0020 | 2 | HG01934.hp2 NA20752.hp1 |
5_prime_UTR_variant | MODIFIER | c.-44G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/11 | 10571 | chr6 | 170306820 | |||||
| chr6:170404594
|
A | T | 14 | a0001c0001t0008a0001c0001t0009a0001c0001t0010others(11): Show | 44 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*4A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 10/11 | 4 | chr6 | 170404594 | |||||
| chr6:170404797
|
C | G | 3 | a0001c0002t0007a0001c0002t0030a0002c0003t0007 | 14 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*46C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 207 | chr6 | 170404797 | |||||
| chr6:170404863
|
G | A | 2 | a0001c0001t0006a0001c0018t0006 | 14 | HG00642.hp2 HG01361.hp2 HG01496.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*112G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 273 | chr6 | 170404863 | |||||
| chr6:170404919
|
T | C | 14 | a0001c0001t0008a0001c0001t0009a0001c0001t0010others(11): Show | 44 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*168T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 329 | chr6 | 170404919 | |||||
| chr6:170405052
|
T | C | 14 | a0001c0001t0008a0001c0001t0009a0001c0001t0010others(11): Show | 44 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*301T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 462 | chr6 | 170405052 | |||||
| chr6:170405167
|
A | G | 26 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(23): Show | 182 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*416A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 577 | chr6 | 170405167 | |||||
| chr6:170405243
|
T | G | 43 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(40): Show | 245 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*492T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 653 | chr6 | 170405243 | |||||
| chr6:170405587
|
G | A | 2 | a0001c0001t0008a0008c0016t0008 | 9 | HG02015.hp1 HG02129.hp1 HG02155.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*836G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 997 | chr6 | 170405587 | |||||
| chr6:170405633
|
A | G | 14 | a0001c0001t0008a0001c0001t0009a0001c0001t0010others(11): Show | 44 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*882A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 1043 | chr6 | 170405633 | |||||
| chr6:170405709
|
C | G | 14 | a0001c0001t0008a0001c0001t0009a0001c0001t0010others(11): Show | 44 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*958C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 1119 | chr6 | 170405709 | |||||
| chr6:170405758
|
C | A | 2 | a0003c0004t0003a0003c0004t0015 | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1007C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 1168 | chr6 | 170405758 | |||||
| chr6:170405805
|
C | T | 14 | a0001c0001t0008a0001c0001t0009a0001c0001t0010others(11): Show | 44 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1054C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 1215 | chr6 | 170405805 | |||||
| chr6:170405900
|
A | C | 1 | a0002c0003t0023 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1149A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 1310 | chr6 | 170405900 | |||||
| chr6:170406013
|
TA | T | 7 | a0001c0001t0005a0001c0001t0006a0001c0001t0014others(4): Show | 34 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1273delA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 1434 | INFO_REALIGN_3_PRIME | chr6 | 170406013 | ||||
| chr6:170406267
|
C | G | 13 | a0001c0001t0008a0001c0001t0009a0001c0001t0010others(10): Show | 41 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1516C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 1677 | chr6 | 170406267 | |||||
| chr6:170406319
|
G | C | 3 | a0001c0001t0008a0001c0001t0016a0008c0016t0008 | 11 | HG01123.hp1 HG01243.hp2 HG02015.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1568G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 1729 | chr6 | 170406319 | |||||
| chr6:170406331
|
C | T | 1 | a0001c0002t0004 | 15 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1580C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 1741 | chr6 | 170406331 | |||||
| chr6:170406423
|
C | T | 1 | a0001c0002t0011 | 3 | HG02615.hp1 HG02818.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1672C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 1833 | chr6 | 170406423 | |||||
| chr6:170406441
|
G | A | 14 | a0001c0001t0008a0001c0001t0009a0001c0001t0010others(11): Show | 44 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1690G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 1851 | chr6 | 170406441 | |||||
| chr6:170406551
|
G | A | 1 | a0001c0001t0026 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1800G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 1961 | chr6 | 170406551 | |||||
| chr6:170406574
|
G | A | 6 | a0001c0001t0010a0001c0002t0010a0001c0009t0017others(3): Show | 11 | HG01099.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1823G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 1984 | chr6 | 170406574 | |||||
| chr6:170406611
|
C | T | 1 | a0001c0002t0024 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1860C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 2021 | chr6 | 170406611 | |||||
| chr6:170406820
|
G | T | 14 | a0001c0001t0008a0001c0001t0009a0001c0001t0010others(11): Show | 44 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2069G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 2230 | chr6 | 170406820 | |||||
| chr6:170406847
|
A | C | 1 | a0001c0001t0027 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2096A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 2257 | chr6 | 170406847 | |||||
| chr6:170406982
|
A | G | 1 | a0002c0003t0022 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2231A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 2392 | chr6 | 170406982 | |||||
| chr6:170407025
|
C | T | 1 | a0003c0004t0015 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2274C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 11/11 | 2435 | chr6 | 170407025 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:170306872
|
T | C | 165 | a0001c0001t0010g0083a0001c0001t0010g0095a0001c0001t0010g0096others(162): Show | 169 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.-22+30T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170306872 | ||||||
| chr6:170306930
|
G | T | 67 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(64): Show | 69 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.-22+88G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170306930 | ||||||
| chr6:170307009
|
A | G | 1 | a0001c0001t0009g0278 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-22+167A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170307009 | ||||||
| chr6:170307015
|
T | C | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.-22+173T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170307015 | ||||||
| chr6:170307126
|
T | C | 7 | a0001c0001t0005g0171a0001c0001t0006g0172a0001c0001t0006g0173others(4): Show | 7 | HG01175.hp1 HG01361.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+284T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170307126 | ||||||
| chr6:170307133
|
C | T | 2 | a0001c0002t0001g0105a0001c0002t0004g0104 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-22+291C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170307133 | ||||||
| chr6:170307169
|
C | T | 6 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 6 | HG02572.hp2 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22+327C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170307169 | ||||||
| chr6:170307237
|
A | G | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-22+395A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170307237 | ||||||
| chr6:170307293
|
C | T | 1 | a0001c0001t0008g0271 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-22+451C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170307293 | ||||||
| chr6:170307360
|
G | T | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-22+518G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170307360 | ||||||
| chr6:170307371
|
A | T | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-22+529A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170307371 | ||||||
| chr6:170307414
|
C | G | 1 | a0001c0002t0001g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-22+572C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170307414 | ||||||
| chr6:170307604
|
T | A | 32 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(29): Show | 32 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.-22+762T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170307604 | ||||||
| chr6:170307619
|
G | A | 5 | a0003c0004t0003g0152a0003c0004t0003g0153a0003c0004t0003g0154others(2): Show | 5 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+777G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170307619 | ||||||
| chr6:170307693
|
G | T | 1 | a0001c0002t0001g0100 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-22+851G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170307693 | ||||||
| chr6:170307722
|
G | A | 7 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+880G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170307722 | ||||||
| chr6:170307965
|
C | T | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-22+1123C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170307965 | ||||||
| chr6:170308166
|
C | T | 2 | a0001c0008t0001g0098a0001c0008t0001g0099 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-22+1324C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170308166 | ||||||
| chr6:170308207
|
C | T | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-22+1365C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170308207 | ||||||
| chr6:170308210
|
C | G | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.-22+1368C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170308210 | ||||||
| chr6:170308299
|
G | T | 1 | a0001c0002t0001g0100 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-22+1457G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170308299 | ||||||
| chr6:170308328
|
C | A | 2 | a0001c0002t0001g0105a0001c0002t0004g0104 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-22+1486C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170308328 | ||||||
| chr6:170308329
|
GCACACCC others(5): Show |
G | 67 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(64): Show | 69 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.-22+1496_-22+1507d others(14): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 170308329 | |||||
| chr6:170308384
|
T | C | 2 | a0001c0002t0013g0039a0001c0002t0013g0040 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-22+1542T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170308384 | ||||||
| chr6:170308522
|
A | G | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.-22+1680A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170308522 | ||||||
| chr6:170308563
|
A | T | 1 | a0001c0002t0001g0100 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-22+1721A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170308563 | ||||||
| chr6:170308580
|
A | G | 67 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(64): Show | 69 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.-22+1738A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170308580 | ||||||
| chr6:170308886
|
T | A | 1 | a0001c0002t0001g0100 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-22+2044T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170308886 | ||||||
| chr6:170309107
|
C | T | 85 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(82): Show | 86 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-22+2265C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170309107 | ||||||
| chr6:170309273
|
C | G | 1 | a0001c0002t0001g0097 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-22+2431C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170309273 | ||||||
| chr6:170309284
|
A | G | 2 | a0001c0002t0013g0039a0001c0002t0013g0040 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-22+2442A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170309284 | ||||||
| chr6:170309295
|
AT | A | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.-22+2459delT | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 170309295 | |||||
| chr6:170309634
|
A | C | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-22+2792A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170309634 | ||||||
| chr6:170309664
|
G | T | 5 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(2): Show | 5 | HG00738.hp1 HG00741.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+2822G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170309664 | ||||||
| chr6:170309847
|
T | C | 33 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(30): Show | 33 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.-22+3005T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170309847 | ||||||
| chr6:170309975
|
A | G | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.-22+3133A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170309975 | ||||||
| chr6:170310109
|
A | G | 1 | a0001c0002t0001g0094 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-22+3267A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170310109 | ||||||
| chr6:170310128
|
G | T | 1 | a0001c0001t0008g0200 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-22+3286G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170310128 | ||||||
| chr6:170310167
|
A | C | 5 | a0001c0002t0029g0091a0001c0008t0001g0098a0001c0008t0001g0099others(2): Show | 5 | HG02886.hp1 HG03139.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+3325A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170310167 | ||||||
| chr6:170310168
|
A | G | 270 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(267): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.-22+3326A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170310168 | ||||||
| chr6:170310189
|
G | A | 6 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(3): Show | 6 | NA18952.hp2 NA19068.hp1 NA19074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22+3347G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170310189 | ||||||
| chr6:170310273
|
T | G | 59 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(56): Show | 60 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.-22+3431T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170310273 | ||||||
| chr6:170310417
|
C | T | 2 | a0001c0002t0001g0037a0001c0002t0001g0038 | 2 | HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-22+3575C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170310417 | ||||||
| chr6:170310554
|
C | T | 5 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(2): Show | 5 | HG00738.hp1 HG00741.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+3712C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170310554 | ||||||
| chr6:170310752
|
A | G | 53 | a0001c0002t0001g0105a0001c0002t0004g0104a0001c0002t0029g0091others(50): Show | 54 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.-22+3910A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170310752 | ||||||
| chr6:170310915
|
G | A | 67 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(64): Show | 69 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.-22+4073G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170310915 | ||||||
| chr6:170310947
|
G | C | 44 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(41): Show | 45 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(42): Show |
intron_variant | MODIFIER | c.-22+4105G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170310947 | ||||||
| chr6:170310995
|
C | G | 3 | a0002c0003t0002g0148a0002c0003t0002g0149a0002c0003t0002g0150 | 3 | NA18975.hp1 NA18998.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-22+4153C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170310995 | ||||||
| chr6:170311001
|
G | A | 86 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(83): Show | 87 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.-22+4159G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170311001 | ||||||
| chr6:170311232
|
C | G | 27 | a0001c0001t0001g0245a0001c0001t0001g0247a0001c0001t0001g0248others(24): Show | 27 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.-22+4390C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170311232 | ||||||
| chr6:170311386
|
T | G | 67 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(64): Show | 69 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.-22+4544T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170311386 | ||||||
| chr6:170311436
|
C | G | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-22+4594C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170311436 | ||||||
| chr6:170311484
|
C | T | 33 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(30): Show | 33 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-22+4642C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170311484 | ||||||
| chr6:170311662
|
G | A | 3 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0001g0043 | 3 | HG02965.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-22+4820G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170311662 | ||||||
| chr6:170311669
|
A | G | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.-22+4827A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170311669 | ||||||
| chr6:170311855
|
A | C | 2 | a0001c0009t0017g0093a0001c0009t0018g0092 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-22+5013A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170311855 | ||||||
| chr6:170311903
|
C | A | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.-22+5061C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170311903 | ||||||
| chr6:170311960
|
C | T | 1 | a0001c0002t0001g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-22+5118C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170311960 | ||||||
| chr6:170312034
|
C | T | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.-22+5192C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170312034 | ||||||
| chr6:170312069
|
A | G | 270 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(267): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.-22+5227A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170312069 | ||||||
| chr6:170312156
|
A | C | 2 | a0001c0009t0017g0093a0001c0009t0018g0092 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-21-5214A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170312156 | ||||||
| chr6:170312161
|
T | C | 36 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0005g0171others(33): Show | 36 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.-21-5209T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170312161 | ||||||
| chr6:170312324
|
A | G | 1 | a0001c0002t0001g0100 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-21-5046A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170312324 | ||||||
| chr6:170312577
|
C | A | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21-4793C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170312577 | ||||||
| chr6:170312613
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-21-4757C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170312613 | ||||||
| chr6:170312731
|
TG | T | 58 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(55): Show | 59 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.-21-4638delG | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170312731 | ||||||
| chr6:170312791
|
T | C | 156 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(153): Show | 160 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.-21-4579T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170312791 | ||||||
| chr6:170312848
|
G | A | 1 | a0001c0001t0009g0188 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-21-4522G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170312848 | ||||||
| chr6:170312866
|
T | G | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-21-4504T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170312866 | ||||||
| chr6:170313077
|
C | T | 3 | a0001c0002t0029g0091a0001c0008t0001g0098a0001c0008t0001g0099 | 3 | HG02886.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-21-4293C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170313077 | ||||||
| chr6:170313216
|
C | T | 1 | a0001c0002t0001g0082 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-21-4154C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170313216 | ||||||
| chr6:170313309
|
G | T | 1 | a0004c0005t0009g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-21-4061G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170313309 | ||||||
| chr6:170313583
|
T | C | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-21-3787T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170313583 | ||||||
| chr6:170313590
|
T | C | 6 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0001g0043others(3): Show | 6 | HG02145.hp2 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-3780T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170313590 | ||||||
| chr6:170313619
|
G | A | 1 | a0001c0001t0002g0244 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-21-3751G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170313619 | ||||||
| chr6:170313678
|
A | G | 26 | a0001c0002t0001g0024a0001c0002t0001g0031a0001c0002t0001g0032others(23): Show | 26 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.-21-3692A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170313678 | ||||||
| chr6:170313834
|
C | G | 53 | a0001c0002t0001g0105a0001c0002t0004g0104a0001c0002t0029g0091others(50): Show | 54 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.-21-3536C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170313834 | ||||||
| chr6:170313842
|
G | A | 5 | a0001c0002t0029g0091a0001c0008t0001g0098a0001c0008t0001g0099others(2): Show | 5 | HG02886.hp1 HG03139.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-3528G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170313842 | ||||||
| chr6:170313946
|
C | T | 1 | a0001c0002t0001g0035 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-21-3424C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170313946 | ||||||
| chr6:170313947
|
G | A | 1 | a0001c0001t0006g0201 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-21-3423G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170313947 | ||||||
| chr6:170313953
|
T | C | 270 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(267): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.-21-3417T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170313953 | ||||||
| chr6:170313979
|
C | T | 1 | a0001c0002t0001g0081 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-21-3391C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170313979 | ||||||
| chr6:170314030
|
A | G | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG00738.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-21-3340A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170314030 | ||||||
| chr6:170314269
|
C | G | 1 | a0002c0003t0002g0147 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-21-3101C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170314269 | ||||||
| chr6:170314606
|
C | T | 1 | a0001c0008t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-21-2764C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170314606 | ||||||
| chr6:170314731
|
A | G | 1 | a0002c0003t0002g0146 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-21-2639A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170314731 | ||||||
| chr6:170314848
|
G | A | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21-2522G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170314848 | ||||||
| chr6:170314932
|
T | C | 1 | a0001c0001t0025g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-21-2438T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170314932 | ||||||
| chr6:170315068
|
C | T | 2 | a0001c0002t0001g0105a0001c0002t0004g0104 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-21-2302C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170315068 | ||||||
| chr6:170315117
|
G | A | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21-2253G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170315117 | ||||||
| chr6:170315236
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-21-2134C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170315236 | ||||||
| chr6:170315501
|
T | C | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-21-1869T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170315501 | ||||||
| chr6:170315577
|
C | T | 70 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(67): Show | 73 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-21-1793C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170315577 | ||||||
| chr6:170315640
|
CCTT | C | 5 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(2): Show | 6 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-1727_-21-1725d others(5): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 170315640 | |||||
| chr6:170315660
|
A | G | 1 | a0001c0002t0004g0034 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-21-1710A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170315660 | ||||||
| chr6:170315682
|
A | G | 70 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(67): Show | 73 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-21-1688A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170315682 | ||||||
| chr6:170315711
|
A | T | 70 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(67): Show | 73 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-21-1659A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170315711 | ||||||
| chr6:170315726
|
A | G | 2 | a0001c0002t0001g0105a0001c0002t0004g0104 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-21-1644A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170315726 | ||||||
| chr6:170315852
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-21-1518C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170315852 | ||||||
| chr6:170315926
|
G | A | 69 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(66): Show | 72 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.-21-1444G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170315926 | ||||||
| chr6:170315946
|
G | A | 41 | a0001c0002t0001g0001a0001c0002t0001g0046a0001c0002t0001g0047others(38): Show | 42 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(39): Show |
intron_variant | MODIFIER | c.-21-1424G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170315946 | ||||||
| chr6:170316038
|
A | C | 1 | a0001c0002t0001g0038 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-21-1332A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170316038 | ||||||
| chr6:170316058
|
C | CA | 80 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(77): Show | 82 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.-21-1288dupA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 170316058 | |||||
| chr6:170316058
|
C | CAA | 36 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0250others(33): Show | 36 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.-21-1289_-21-1288d others(4): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 170316058 | |||||
| chr6:170316058
|
C | CAAA | 15 | a0001c0001t0001g0245a0001c0001t0001g0247a0001c0001t0001g0248others(12): Show | 15 | HG00738.hp1 HG00741.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.-21-1290_-21-1288d others(5): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 170316058 | |||||
| chr6:170316058
|
CA | C | 13 | a0001c0001t0008g0010a0001c0001t0008g0194a0001c0001t0008g0195others(10): Show | 14 | HG01081.hp2 HG01123.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21-1288delA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 170316058 | |||||
| chr6:170316058
|
CAAAA | C | 66 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0109others(63): Show | 69 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.-21-1291_-21-1288d others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 170316058 | |||||
| chr6:170316096
|
A | G | 2 | a0001c0002t0001g0105a0001c0002t0004g0104 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-21-1274A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170316096 | ||||||
| chr6:170316210
|
A | G | 70 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(67): Show | 73 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-21-1160A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170316210 | ||||||
| chr6:170316346
|
T | C | 72 | a0001c0002t0001g0105a0001c0002t0004g0104a0002c0003t0001g0134others(69): Show | 75 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.-21-1024T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170316346 | ||||||
| chr6:170316438
|
A | AG | 72 | a0001c0002t0001g0105a0001c0002t0004g0104a0002c0003t0001g0134others(69): Show | 75 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.-21-932_-21-931ins others(1): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170316438 | ||||||
| chr6:170316783
|
T | C | 2 | a0001c0002t0001g0105a0001c0002t0004g0104 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-21-587T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170316783 | ||||||
| chr6:170316879
|
C | G | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-21-491C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170316879 | ||||||
| chr6:170317137
|
T | C | 165 | a0001c0001t0010g0083a0001c0001t0010g0095a0001c0001t0010g0096others(162): Show | 169 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.-21-233T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170317137 | ||||||
| chr6:170317200
|
A | G | 2 | a0001c0002t0001g0105a0001c0002t0004g0104 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-21-170A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 1/10 | chr6 | 170317200 | ||||||
| chr6:170319143
|
C | A | 33 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(30): Show | 33 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1734+19C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170319143 | ||||||
| chr6:170319394
|
T | C | 72 | a0001c0002t0001g0105a0001c0002t0004g0104a0002c0003t0001g0134others(69): Show | 75 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1734+270T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170319394 | ||||||
| chr6:170319543
|
A | G | 5 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(2): Show | 6 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1734+419A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170319543 | ||||||
| chr6:170319560
|
C | T | 30 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(27): Show | 30 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1734+436C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170319560 | ||||||
| chr6:170319803
|
C | T | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1734+679C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170319803 | ||||||
| chr6:170320036
|
A | G | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1734+912A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170320036 | ||||||
| chr6:170320037
|
C | T | 67 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(64): Show | 69 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1734+913C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170320037 | ||||||
| chr6:170320070
|
A | G | 1 | a0001c0002t0001g0036 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1734+946A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170320070 | ||||||
| chr6:170320104
|
G | T | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1734+980G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170320104 | ||||||
| chr6:170320171
|
A | G | 1 | a0009c0014t0009g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1734+1047A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170320171 | ||||||
| chr6:170320285
|
T | C | 1 | a0009c0014t0009g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1734+1161T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170320285 | ||||||
| chr6:170320389
|
G | A | 10 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0032others(7): Show | 10 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1734+1265G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170320389 | ||||||
| chr6:170320559
|
C | G | 67 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(64): Show | 69 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1734+1435C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170320559 | ||||||
| chr6:170320571
|
G | C | 107 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(104): Show | 110 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1734+1447G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170320571 | ||||||
| chr6:170320607
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1734+1483G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170320607 | ||||||
| chr6:170320624
|
T | A | 1 | a0002c0003t0002g0109 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1734+1500T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170320624 | ||||||
| chr6:170320656
|
C | G | 5 | a0002c0003t0002g0109a0002c0003t0002g0141a0002c0003t0002g0142others(2): Show | 5 | HG01123.hp2 HG01261.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1734+1532C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170320656 | ||||||
| chr6:170320658
|
AAC | A | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1734+1538_1734+153 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 170320658 | |||||
| chr6:170320720
|
T | C | 2 | a0006c0010t0010g0019a0006c0010t0010g0020 | 2 | HG01099.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1734+1596T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170320720 | ||||||
| chr6:170320853
|
AG | A | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1734+1734delG | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 170320853 | |||||
| chr6:170321082
|
A | G | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1734+1958A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170321082 | ||||||
| chr6:170321093
|
G | A | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1734+1969G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170321093 | ||||||
| chr6:170321186
|
C | T | 2 | a0001c0002t0004g0028a0001c0002t0004g0029 | 2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1735-1893C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170321186 | ||||||
| chr6:170321329
|
A | G | 3 | a0001c0002t0029g0091a0001c0008t0001g0098a0001c0008t0001g0099 | 3 | HG02886.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1735-1750A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170321329 | ||||||
| chr6:170321333
|
G | C | 67 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(64): Show | 69 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1735-1746G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170321333 | ||||||
| chr6:170321340
|
C | G | 1 | a0001c0001t0001g0248 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1735-1739C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170321340 | ||||||
| chr6:170321489
|
T | C | 72 | a0001c0002t0001g0105a0001c0002t0004g0104a0002c0003t0001g0134others(69): Show | 75 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1735-1590T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170321489 | ||||||
| chr6:170321535
|
G | A | 3 | a0001c0002t0029g0091a0001c0008t0001g0098a0001c0008t0001g0099 | 3 | HG02886.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1735-1544G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170321535 | ||||||
| chr6:170321592
|
T | A | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1735-1487T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170321592 | ||||||
| chr6:170321742
|
C | G | 2 | a0001c0009t0017g0093a0001c0009t0018g0092 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1735-1337C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170321742 | ||||||
| chr6:170321794
|
C | T | 67 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(64): Show | 69 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1735-1285C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170321794 | ||||||
| chr6:170321911
|
A | C | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1735-1168A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170321911 | ||||||
| chr6:170321921
|
T | G | 5 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(2): Show | 6 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1735-1158T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170321921 | ||||||
| chr6:170321931
|
T | C | 279 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(276): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1735-1148T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170321931 | ||||||
| chr6:170321973
|
G | A | 3 | a0001c0001t0001g0245a0001c0001t0001g0250a0001c0001t0005g0249 | 3 | HG03471.hp1 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1735-1106G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170321973 | ||||||
| chr6:170322023
|
C | G | 67 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(64): Show | 69 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1735-1056C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170322023 | ||||||
| chr6:170322097
|
CTACT | C | 5 | a0001c0002t0001g0105a0001c0002t0004g0104a0005c0007t0012g0002others(2): Show | 6 | HG00639.hp1 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1735-975_1735-972d others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 170322097 | |||||
| chr6:170322164
|
C | T | 8 | a0001c0001t0010g0083a0004c0005t0001g0084a0004c0005t0001g0085others(5): Show | 8 | HG02723.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1735-915C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170322164 | ||||||
| chr6:170322270
|
A | G | 72 | a0001c0002t0001g0105a0001c0002t0004g0104a0002c0003t0001g0134others(69): Show | 75 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1735-809A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170322270 | ||||||
| chr6:170322315
|
C | T | 104 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(101): Show | 107 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1735-764C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170322315 | ||||||
| chr6:170322423
|
T | A | 1 | a0001c0001t0001g0251 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1735-656T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170322423 | ||||||
| chr6:170322530
|
A | G | 6 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 6 | HG02572.hp2 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1735-549A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170322530 | ||||||
| chr6:170322535
|
G | C | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1735-544G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170322535 | ||||||
| chr6:170322552
|
G | A | 3 | a0001c0002t0029g0091a0001c0008t0001g0098a0001c0008t0001g0099 | 3 | HG02886.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1735-527G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170322552 | ||||||
| chr6:170322585
|
G | A | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1735-494G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170322585 | ||||||
| chr6:170322638
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1735-441T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170322638 | ||||||
| chr6:170322686
|
A | G | 1 | a0001c0002t0004g0034 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1735-393A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170322686 | ||||||
| chr6:170322746
|
T | G | 72 | a0001c0002t0001g0105a0001c0002t0004g0104a0002c0003t0001g0134others(69): Show | 75 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1735-333T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170322746 | ||||||
| chr6:170322828
|
A | T | 1 | a0001c0002t0001g0050 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1735-251A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170322828 | ||||||
| chr6:170322917
|
A | G | 1 | a0004c0005t0009g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1735-162A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170322917 | ||||||
| chr6:170322976
|
G | T | 44 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(41): Show | 45 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(42): Show |
intron_variant | MODIFIER | c.1735-103G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170322976 | ||||||
| chr6:170323033
|
A | G | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1735-46A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 2/10 | chr6 | 170323033 | ||||||
| chr6:170323295
|
A | G | 67 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(64): Show | 69 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1915+36A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170323295 | ||||||
| chr6:170323660
|
A | G | 1 | a0001c0002t0001g0078 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1915+401A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170323660 | ||||||
| chr6:170323782
|
C | T | 67 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(64): Show | 69 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1915+523C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170323782 | ||||||
| chr6:170323860
|
C | A | 67 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(64): Show | 69 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1915+601C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170323860 | ||||||
| chr6:170323952
|
T | G | 5 | a0001c0002t0001g0105a0001c0002t0004g0104a0005c0007t0012g0002others(2): Show | 6 | HG00639.hp1 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1915+693T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170323952 | ||||||
| chr6:170324073
|
G | A | 1 | a0001c0001t0008g0200 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1915+814G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170324073 | ||||||
| chr6:170324319
|
A | G | 7 | a0001c0001t0001g0247a0001c0001t0001g0259a0001c0001t0001g0260others(4): Show | 7 | HG00323.hp1 HG01074.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.1915+1060A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170324319 | ||||||
| chr6:170324476
|
C | T | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1915+1217C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170324476 | ||||||
| chr6:170324494
|
G | C | 1 | a0001c0001t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1915+1235G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170324494 | ||||||
| chr6:170324575
|
A | C | 1 | a0001c0002t0001g0077 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1915+1316A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170324575 | ||||||
| chr6:170325228
|
A | G | 1 | a0001c0001t0006g0177 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1915+1969A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170325228 | ||||||
| chr6:170325312
|
G | A | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1915+2053G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170325312 | ||||||
| chr6:170325532
|
C | CT | 47 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0107others(44): Show | 49 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1915+2276dupT | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 170325532 | |||||
| chr6:170325535
|
T | TA | 76 | a0001c0001t0001g0204a0001c0001t0001g0231a0001c0001t0001g0245others(73): Show | 77 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.1915+2293dupA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 170325535 | |||||
| chr6:170325535
|
TA | T | 10 | a0001c0001t0008g0192a0001c0002t0001g0012a0001c0002t0001g0013others(7): Show | 10 | HG01069.hp1 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1915+2293delA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 170325535 | |||||
| chr6:170325536
|
A | T | 22 | a0001c0002t0001g0105a0002c0003t0002g0109a0003c0004t0003g0005others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1915+2277A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170325536 | ||||||
| chr6:170325537
|
A | T | 2 | a0001c0002t0004g0104a0003c0004t0015g0155 | 2 | HG01069.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1915+2278A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170325537 | ||||||
| chr6:170325601
|
G | A | 70 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(67): Show | 73 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.1915+2342G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170325601 | ||||||
| chr6:170325851
|
CA | C | 86 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(83): Show | 87 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1915+2609delA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 170325851 | |||||
| chr6:170325872
|
G | T | 6 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0001g0043others(3): Show | 6 | HG02145.hp2 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1915+2613G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170325872 | ||||||
| chr6:170325972
|
A | G | 2 | a0001c0002t0001g0105a0001c0002t0004g0104 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1915+2713A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170325972 | ||||||
| chr6:170326330
|
C | T | 2 | a0001c0002t0001g0105a0001c0002t0004g0104 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1915+3071C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170326330 | ||||||
| chr6:170326415
|
G | A | 2 | a0001c0002t0001g0105a0001c0002t0004g0104 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1915+3156G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170326415 | ||||||
| chr6:170326448
|
T | G | 6 | a0001c0002t0001g0055a0001c0002t0001g0056a0001c0002t0001g0057others(3): Show | 6 | HG02293.hp2 NA18612.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.1915+3189T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170326448 | ||||||
| chr6:170326558
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1915+3299C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170326558 | ||||||
| chr6:170326613
|
A | G | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1915+3354A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170326613 | ||||||
| chr6:170326664
|
A | G | 1 | a0002c0003t0002g0140 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1915+3405A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170326664 | ||||||
| chr6:170326812
|
C | T | 199 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(196): Show | 203 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1915+3553C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170326812 | ||||||
| chr6:170326826
|
A | G | 2 | a0002c0003t0002g0139a0002c0003t0002g0147 | 2 | HG01070.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1915+3567A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170326826 | ||||||
| chr6:170326887
|
C | T | 70 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(67): Show | 73 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.1916-3562C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170326887 | ||||||
| chr6:170326975
|
C | T | 3 | a0001c0002t0029g0091a0001c0008t0001g0098a0001c0008t0001g0099 | 3 | HG02886.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1916-3474C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170326975 | ||||||
| chr6:170327055
|
T | C | 70 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(67): Show | 73 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.1916-3394T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170327055 | ||||||
| chr6:170327062
|
T | C | 2 | a0006c0010t0010g0019a0006c0010t0010g0020 | 2 | HG01099.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1916-3387T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170327062 | ||||||
| chr6:170327099
|
G | T | 1 | a0001c0002t0001g0076 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1916-3350G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170327099 | ||||||
| chr6:170327236
|
C | T | 1 | a0001c0002t0011g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1916-3213C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170327236 | ||||||
| chr6:170327263
|
A | G | 1 | a0001c0001t0006g0176 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1916-3186A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170327263 | ||||||
| chr6:170327268
|
G | T | 1 | a0001c0001t0006g0176 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1916-3181G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170327268 | ||||||
| chr6:170327288
|
C | T | 1 | a0001c0001t0006g0176 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1916-3161C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170327288 | ||||||
| chr6:170327293
|
A | G | 1 | a0001c0001t0006g0176 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1916-3156A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170327293 | ||||||
| chr6:170327464
|
C | T | 70 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(67): Show | 73 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.1916-2985C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170327464 | ||||||
| chr6:170327523
|
C | T | 2 | a0001c0002t0013g0039a0001c0002t0013g0040 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1916-2926C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170327523 | ||||||
| chr6:170327535
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1916-2914G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170327535 | ||||||
| chr6:170327599
|
G | GCTGCTGT others(369): Show |
1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1916-2695_1916-269 others(380): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 170327599 | |||||
| chr6:170327628
|
C | CGCAGGCT others(87): Show |
2 | a0004c0005t0001g0084a0004c0005t0009g0090 | 2 | HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1916-2759_1916-275 others(98): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 170327628 | |||||
| chr6:170327640
|
C | T | 23 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(20): Show | 24 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1916-2809C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170327640 | ||||||
| chr6:170327662
|
A | AGAGTGAG others(76): Show |
5 | a0004c0005t0001g0085a0004c0005t0001g0086a0004c0005t0001g0087others(2): Show | 5 | HG02965.hp2 HG03041.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1916-2759_1916-275 others(87): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 170327662 | |||||
| chr6:170327736
|
C | T | 1 | a0001c0002t0001g0075 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1916-2713C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170327736 | ||||||
| chr6:170327821
|
G | A | 2 | a0001c0002t0013g0039a0001c0002t0013g0040 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1916-2628G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170327821 | ||||||
| chr6:170327829
|
C | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG00280.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1916-2620C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170327829 | ||||||
| chr6:170328038
|
A | G | 73 | a0001c0001t0009g0191a0001c0002t0013g0039a0001c0002t0013g0040others(70): Show | 76 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.1916-2411A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170328038 | ||||||
| chr6:170328071
|
TACTGTA | T | 51 | a0001c0002t0013g0039a0001c0002t0013g0040a0002c0003t0001g0134others(48): Show | 53 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.1916-2374_1916-236 others(10): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 170328071 | |||||
| chr6:170328163
|
C | G | 6 | a0003c0004t0003g0005a0003c0004t0003g0166a0003c0004t0003g0167others(3): Show | 7 | NA18942.hp1 NA18944.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.1916-2286C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170328163 | ||||||
| chr6:170328177
|
ATTCT | A | 44 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(41): Show | 45 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(42): Show |
intron_variant | MODIFIER | c.1916-2265_1916-226 others(8): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 170328177 | |||||
| chr6:170328188
|
A | G | 33 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(30): Show | 33 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1916-2261A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170328188 | ||||||
| chr6:170328193
|
A | G | 5 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(2): Show | 6 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1916-2256A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170328193 | ||||||
| chr6:170328305
|
G | A | 1 | a0001c0002t0001g0081 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1916-2144G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170328305 | ||||||
| chr6:170328389
|
G | C | 13 | a0001c0001t0010g0083a0001c0002t0004g0104a0002c0003t0002g0107others(10): Show | 13 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.1916-2060G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170328389 | ||||||
| chr6:170328535
|
T | C | 62 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0001g0043others(59): Show | 64 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.1916-1914T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170328535 | ||||||
| chr6:170328549
|
T | C | 5 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(2): Show | 6 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1916-1900T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170328549 | ||||||
| chr6:170328572
|
A | G | 2 | a0001c0002t0001g0077a0001c0002t0001g0097 | 2 | HG02293.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1916-1877A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170328572 | ||||||
| chr6:170328610
|
TC | T | 26 | a0001c0002t0001g0105a0001c0002t0004g0104a0003c0004t0003g0005others(23): Show | 28 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1916-1837delC | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr6 | 170328610 | |||||
| chr6:170328687
|
C | T | 2 | a0001c0001t0005g0202a0001c0001t0005g0225 | 2 | HG00735.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1916-1762C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170328687 | ||||||
| chr6:170328800
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1916-1649G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170328800 | ||||||
| chr6:170328848
|
A | T | 2 | a0002c0003t0007g0112a0002c0003t0007g0145 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1916-1601A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170328848 | ||||||
| chr6:170328941
|
A | C | 1 | a0001c0001t0016g0199 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1916-1508A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170328941 | ||||||
| chr6:170328950
|
A | G | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1916-1499A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170328950 | ||||||
| chr6:170329127
|
T | C | 168 | a0001c0001t0010g0083a0001c0001t0010g0095a0001c0001t0010g0096others(165): Show | 172 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.1916-1322T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170329127 | ||||||
| chr6:170329134
|
T | A | 1 | a0001c0002t0001g0059 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1916-1315T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170329134 | ||||||
| chr6:170329169
|
T | C | 1 | a0004c0005t0001g0086 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1916-1280T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170329169 | ||||||
| chr6:170329234
|
C | T | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1916-1215C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170329234 | ||||||
| chr6:170329297
|
G | A | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1916-1152G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170329297 | ||||||
| chr6:170329412
|
A | G | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1916-1037A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170329412 | ||||||
| chr6:170329450
|
T | A | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1916-999T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170329450 | ||||||
| chr6:170329509
|
C | T | 44 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(41): Show | 45 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(42): Show |
intron_variant | MODIFIER | c.1916-940C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170329509 | ||||||
| chr6:170329623
|
G | A | 2 | a0001c0001t0005g0202a0001c0001t0005g0225 | 2 | HG00735.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1916-826G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170329623 | ||||||
| chr6:170329647
|
C | T | 5 | a0001c0002t0029g0091a0001c0008t0001g0098a0001c0008t0001g0099others(2): Show | 5 | HG02886.hp1 HG03139.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1916-802C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170329647 | ||||||
| chr6:170329711
|
T | C | 1 | a0001c0001t0010g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1916-738T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170329711 | ||||||
| chr6:170329770
|
G | A | 1 | a0001c0002t0001g0060 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1916-679G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170329770 | ||||||
| chr6:170329780
|
C | T | 1 | a0001c0002t0001g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1916-669C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170329780 | ||||||
| chr6:170329917
|
T | A | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1916-532T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170329917 | ||||||
| chr6:170329947
|
A | G | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1916-502A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170329947 | ||||||
| chr6:170330002
|
C | T | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1916-447C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170330002 | ||||||
| chr6:170330049
|
C | A | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1916-400C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170330049 | ||||||
| chr6:170330115
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0239a0001c0001t0001g0240others(1): Show | 5 | HG02280.hp2 HG02717.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1916-334A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 3/10 | chr6 | 170330115 | ||||||
| chr6:170330577
|
C | T | 1 | a0001c0002t0001g0100 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2017+27C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170330577 | ||||||
| chr6:170330638
|
T | C | 1 | a0001c0008t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2017+88T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170330638 | ||||||
| chr6:170330698
|
C | A | 47 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(44): Show | 49 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(46): Show |
intron_variant | MODIFIER | c.2017+148C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170330698 | ||||||
| chr6:170330804
|
C | G | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2017+254C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170330804 | ||||||
| chr6:170330865
|
G | A | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2017+315G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170330865 | ||||||
| chr6:170330868
|
GC | G | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2017+322delC | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170330868 | |||||
| chr6:170331032
|
C | T | 30 | a0001c0002t0001g0102a0001c0002t0001g0105a0001c0002t0004g0104others(27): Show | 31 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.2017+482C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170331032 | ||||||
| chr6:170331280
|
C | T | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2017+730C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170331280 | ||||||
| chr6:170331366
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2017+816C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170331366 | ||||||
| chr6:170331916
|
G | A | 6 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 6 | HG02572.hp2 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2017+1366G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170331916 | ||||||
| chr6:170331926
|
G | A | 80 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(77): Show | 82 | HG00099.hp1 HG00558.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.2017+1376G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170331926 | ||||||
| chr6:170331966
|
T | C | 3 | a0001c0002t0029g0091a0001c0008t0001g0098a0001c0008t0001g0099 | 3 | HG02886.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2017+1416T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170331966 | ||||||
| chr6:170331999
|
T | G | 2 | a0001c0002t0013g0039a0001c0002t0013g0040 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2017+1449T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170331999 | ||||||
| chr6:170332125
|
C | T | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2017+1575C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170332125 | ||||||
| chr6:170332191
|
T | G | 1 | a0001c0002t0001g0046 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2017+1641T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170332191 | ||||||
| chr6:170332236
|
C | T | 2 | a0001c0009t0017g0093a0001c0009t0018g0092 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2017+1686C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170332236 | ||||||
| chr6:170332368
|
G | T | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2017+1818G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170332368 | ||||||
| chr6:170332375
|
A | G | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2017+1825A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170332375 | ||||||
| chr6:170332435
|
C | T | 1 | a0001c0002t0001g0059 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2017+1885C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170332435 | ||||||
| chr6:170332464
|
G | A | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2017+1914G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170332464 | ||||||
| chr6:170332620
|
C | T | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2017+2070C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170332620 | ||||||
| chr6:170332646
|
C | T | 47 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(44): Show | 49 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(46): Show |
intron_variant | MODIFIER | c.2017+2096C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170332646 | ||||||
| chr6:170332698
|
C | CA | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2017+2159dupA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170332698 | |||||
| chr6:170332723
|
G | A | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2017+2173G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170332723 | ||||||
| chr6:170332919
|
T | A | 5 | a0001c0002t0001g0051a0001c0002t0001g0061a0001c0002t0001g0062others(2): Show | 5 | HG01981.hp1 HG02056.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.2017+2369T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170332919 | ||||||
| chr6:170332937
|
G | A | 2 | a0001c0001t0001g0259a0001c0002t0001g0102 | 2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2017+2387G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170332937 | ||||||
| chr6:170332989
|
A | G | 1 | a0001c0001t0005g0263 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2017+2439A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170332989 | ||||||
| chr6:170333003
|
C | T | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2017+2453C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170333003 | ||||||
| chr6:170333161
|
C | T | 1 | a0002c0003t0023g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2017+2611C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170333161 | ||||||
| chr6:170333162
|
G | GC | 14 | a0001c0001t0001g0207a0001c0001t0005g0202a0001c0001t0005g0208others(11): Show | 14 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.2017+2619dupC | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170333162 | |||||
| chr6:170333169
|
C | T | 2 | a0001c0002t0013g0039a0001c0002t0013g0040 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2017+2619C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170333169 | ||||||
| chr6:170333171
|
C | T | 4 | a0001c0002t0001g0001a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 5 | NA18939.hp2 NA18942.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.2017+2621C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170333171 | ||||||
| chr6:170333176
|
C | G | 1 | a0001c0001t0005g0224 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2017+2626C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170333176 | ||||||
| chr6:170333282
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2017+2732G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170333282 | ||||||
| chr6:170333309
|
A | G | 1 | a0001c0001t0025g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2017+2759A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170333309 | ||||||
| chr6:170333317
|
T | C | 1 | a0009c0014t0009g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2017+2767T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170333317 | ||||||
| chr6:170333492
|
A | G | 1 | a0009c0014t0009g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2017+2942A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170333492 | ||||||
| chr6:170333509
|
A | G | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2017+2959A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170333509 | ||||||
| chr6:170333517
|
C | CT | 13 | a0001c0001t0001g0262a0001c0001t0005g0225a0001c0001t0016g0198others(10): Show | 13 | HG00735.hp2 HG01123.hp1 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.2017+2985dupT | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170333517 | |||||
| chr6:170333517
|
CT | C | 25 | a0001c0001t0001g0234a0001c0001t0001g0259a0001c0001t0027g0210others(22): Show | 26 | HG00733.hp1 HG00735.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2017+2985delT | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170333517 | |||||
| chr6:170333666
|
A | G | 1 | a0002c0003t0002g0137 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2017+3116A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170333666 | ||||||
| chr6:170333717
|
C | T | 89 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(86): Show | 90 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.2017+3167C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170333717 | ||||||
| chr6:170333718
|
G | A | 5 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(2): Show | 6 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2017+3168G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170333718 | ||||||
| chr6:170333782
|
C | CGTATG | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2017+3234_2017+323 others(9): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170333782 | |||||
| chr6:170333802
|
G | A | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2017+3252G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170333802 | ||||||
| chr6:170333861
|
A | G | 1 | a0001c0001t0026g0223 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2017+3311A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170333861 | ||||||
| chr6:170333863
|
A | G | 1 | a0003c0004t0003g0165 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2017+3313A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170333863 | ||||||
| chr6:170333924
|
G | A | 1 | a0001c0001t0006g0172 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2017+3374G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170333924 | ||||||
| chr6:170334096
|
A | G | 1 | a0001c0002t0004g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2017+3546A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170334096 | ||||||
| chr6:170334166
|
A | G | 9 | a0001c0002t0007g0006a0001c0002t0007g0007a0001c0002t0007g0008others(6): Show | 12 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.2017+3616A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170334166 | ||||||
| chr6:170334370
|
A | G | 2 | a0001c0002t0011g0016a0001c0002t0011g0017 | 2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2017+3820A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170334370 | ||||||
| chr6:170334394
|
A | G | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2017+3844A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170334394 | ||||||
| chr6:170334527
|
G | C | 3 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0001g0038 | 3 | HG02615.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2017+3977G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170334527 | ||||||
| chr6:170334547
|
G | GGT | 47 | a0001c0001t0001g0207a0001c0001t0005g0171a0001c0001t0005g0202others(44): Show | 48 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.2017+4023_2017+402 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170334547 | |||||
| chr6:170334547
|
G | GGTGT | 57 | a0001c0001t0005g0221a0001c0001t0006g0222a0001c0002t0001g0001others(54): Show | 58 | HG00673.hp1 HG01069.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.2017+4021_2017+402 others(8): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170334547 | |||||
| chr6:170334547
|
G | GGTGTGT | 4 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0077others(1): Show | 4 | HG02293.hp2 NA18949.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017+4019_2017+402 others(10): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170334547 | |||||
| chr6:170334547
|
GGT | G | 128 | a0001c0001t0001g0230a0001c0001t0001g0245a0001c0001t0001g0247others(125): Show | 134 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.2017+4023_2017+402 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170334547 | |||||
| chr6:170334547
|
GGTGTGT | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0239a0001c0001t0001g0240others(1): Show | 5 | HG02280.hp2 HG02717.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2017+4019_2017+402 others(10): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170334547 | |||||
| chr6:170334614
|
C | T | 1 | a0002c0003t0002g0136 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2017+4064C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170334614 | ||||||
| chr6:170334623
|
G | T | 30 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(27): Show | 30 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2017+4073G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170334623 | ||||||
| chr6:170334640
|
G | T | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2017+4090G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170334640 | ||||||
| chr6:170334738
|
T | G | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017+4188T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170334738 | ||||||
| chr6:170334774
|
C | T | 47 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(44): Show | 49 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(46): Show |
intron_variant | MODIFIER | c.2017+4224C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170334774 | ||||||
| chr6:170334914
|
A | T | 33 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(30): Show | 33 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.2017+4364A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170334914 | ||||||
| chr6:170334953
|
T | A | 8 | a0001c0002t0001g0102a0001c0002t0004g0104a0001c0002t0010g0103others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2017+4403T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170334953 | ||||||
| chr6:170334973
|
A | G | 1 | a0001c0001t0005g0225 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2017+4423A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170334973 | ||||||
| chr6:170335020
|
G | A | 1 | a0001c0008t0001g0098 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2017+4470G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170335020 | ||||||
| chr6:170335035
|
G | GT | 6 | a0001c0001t0006g0209a0001c0002t0001g0079a0001c0008t0001g0098others(3): Show | 6 | HG00642.hp2 HG01099.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2017+4495dupT | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170335035 | |||||
| chr6:170335036
|
T | G | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2017+4486T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170335036 | ||||||
| chr6:170335045
|
T | G | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2017+4495T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170335045 | ||||||
| chr6:170335046
|
G | T | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2017+4496G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170335046 | ||||||
| chr6:170335114
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2017+4564T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170335114 | ||||||
| chr6:170335185
|
G | C | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2017+4635G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170335185 | ||||||
| chr6:170335220
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2017+4670C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170335220 | ||||||
| chr6:170335401
|
G | A | 2 | a0001c0009t0017g0093a0001c0009t0018g0092 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2017+4851G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170335401 | ||||||
| chr6:170335682
|
G | T | 5 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(2): Show | 6 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2017+5132G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170335682 | ||||||
| chr6:170335706
|
G | A | 10 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0032others(7): Show | 10 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2017+5156G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170335706 | ||||||
| chr6:170336031
|
T | C | 1 | a0001c0002t0004g0178 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2017+5481T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170336031 | ||||||
| chr6:170336152
|
G | A | 41 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(38): Show | 42 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.2017+5602G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170336152 | ||||||
| chr6:170336229
|
G | A | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2017+5679G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170336229 | ||||||
| chr6:170336433
|
T | C | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2017+5883T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170336433 | ||||||
| chr6:170336466
|
C | T | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2017+5916C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170336466 | ||||||
| chr6:170336741
|
C | T | 41 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(38): Show | 42 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.2017+6191C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170336741 | ||||||
| chr6:170336862
|
T | A | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017+6312T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170336862 | ||||||
| chr6:170336922
|
G | C | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2017+6372G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170336922 | ||||||
| chr6:170336947
|
G | T | 1 | a0001c0002t0001g0075 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2017+6397G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170336947 | ||||||
| chr6:170337260
|
C | T | 30 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(27): Show | 30 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2017+6710C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170337260 | ||||||
| chr6:170337291
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2017+6741C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170337291 | ||||||
| chr6:170337292
|
G | A | 1 | a0002c0003t0002g0114 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2017+6742G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170337292 | ||||||
| chr6:170337382
|
G | A | 6 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 6 | HG02572.hp2 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2017+6832G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170337382 | ||||||
| chr6:170337396
|
G | A | 1 | a0002c0003t0002g0136 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2017+6846G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170337396 | ||||||
| chr6:170337431
|
G | GC | 5 | a0001c0002t0029g0091a0001c0008t0001g0098a0001c0008t0001g0099others(2): Show | 5 | HG02886.hp1 HG03139.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2017+6883dupC | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170337431 | |||||
| chr6:170337479
|
A | G | 153 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(150): Show | 157 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.2017+6929A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170337479 | ||||||
| chr6:170337515
|
GT | G | 30 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(27): Show | 30 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2017+6969delT | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170337515 | |||||
| chr6:170337638
|
C | T | 2 | a0001c0002t0013g0039a0001c0002t0013g0040 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2017+7088C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170337638 | ||||||
| chr6:170337737
|
G | A | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2017+7187G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170337737 | ||||||
| chr6:170338131
|
A | G | 270 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(267): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.2017+7581A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170338131 | ||||||
| chr6:170338290
|
C | A | 1 | a0001c0002t0011g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2017+7740C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170338290 | ||||||
| chr6:170338595
|
C | T | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2017+8045C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170338595 | ||||||
| chr6:170338719
|
A | G | 1 | a0001c0009t0017g0093 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2017+8169A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170338719 | ||||||
| chr6:170338778
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2017+8228C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170338778 | ||||||
| chr6:170338779
|
G | C | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2017+8229G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170338779 | ||||||
| chr6:170338844
|
C | CT | 93 | a0001c0001t0006g0175a0001c0001t0025g0187a0001c0002t0001g0001others(90): Show | 94 | HG00099.hp1 HG00558.hp1 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.2017+8314dupT | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170338844 | |||||
| chr6:170338844
|
C | CTT | 49 | a0001c0002t0001g0035a0001c0002t0001g0078a0001c0002t0001g0105others(46): Show | 51 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.2017+8313_2017+831 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170338844 | |||||
| chr6:170338844
|
C | CTTT | 7 | a0001c0002t0001g0024a0002c0003t0001g0134a0002c0003t0002g0135others(4): Show | 7 | HG00673.hp2 HG01099.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2017+8312_2017+831 others(7): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170338844 | |||||
| chr6:170338887
|
C | T | 27 | a0001c0001t0001g0204a0001c0001t0001g0245a0001c0001t0001g0247others(24): Show | 27 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.2017+8337C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170338887 | ||||||
| chr6:170339195
|
A | T | 2 | a0002c0003t0002g0133a0002c0003t0002g0135 | 2 | HG00673.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.2017+8645A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170339195 | ||||||
| chr6:170339401
|
A | G | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2018-8750A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170339401 | ||||||
| chr6:170339487
|
C | A | 1 | a0001c0001t0001g0265 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2018-8664C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170339487 | ||||||
| chr6:170339512
|
G | T | 23 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(20): Show | 23 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.2018-8639G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170339512 | ||||||
| chr6:170339537
|
C | T | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2018-8614C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170339537 | ||||||
| chr6:170339567
|
T | C | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2018-8584T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170339567 | ||||||
| chr6:170339668
|
A | C | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2018-8483A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170339668 | ||||||
| chr6:170339765
|
C | T | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2018-8386C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170339765 | ||||||
| chr6:170339778
|
C | CA | 7 | a0001c0001t0001g0241a0001c0001t0001g0262a0001c0001t0006g0175others(4): Show | 7 | HG00733.hp1 HG01361.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.2018-8354dupA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170339778 | |||||
| chr6:170339778
|
CA | C | 88 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(85): Show | 90 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.2018-8354delA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170339778 | |||||
| chr6:170339803
|
T | A | 1 | a0001c0001t0006g0201 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2018-8348T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170339803 | ||||||
| chr6:170339819
|
C | G | 1 | a0001c0002t0029g0091 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2018-8332C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170339819 | ||||||
| chr6:170339944
|
G | A | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2018-8207G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170339944 | ||||||
| chr6:170339972
|
G | A | 3 | a0001c0001t0005g0213a0001c0001t0005g0214a0001c0001t0005g0221 | 3 | HG00639.hp2 HG01109.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2018-8179G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170339972 | ||||||
| chr6:170340266
|
A | T | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2018-7885A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170340266 | ||||||
| chr6:170340267
|
A | C | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2018-7884A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170340267 | ||||||
| chr6:170340388
|
CTGTA | C | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2018-7762_2018-775 others(8): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170340388 | ||||||
| chr6:170340389
|
T | C | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2018-7762T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170340389 | ||||||
| chr6:170340393
|
A | C | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2018-7758A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170340393 | ||||||
| chr6:170340413
|
G | A | 3 | a0003c0004t0003g0157a0003c0004t0003g0158a0003c0004t0003g0165 | 3 | NA18970.hp1 NA18982.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.2018-7738G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170340413 | ||||||
| chr6:170340428
|
G | A | 1 | a0002c0003t0001g0134 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2018-7723G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170340428 | ||||||
| chr6:170340622
|
G | A | 30 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(27): Show | 30 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2018-7529G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170340622 | ||||||
| chr6:170340811
|
C | T | 2 | a0001c0002t0001g0071a0001c0017t0001g0080 | 2 | NA18747.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2018-7340C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170340811 | ||||||
| chr6:170340958
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2018-7193C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170340958 | ||||||
| chr6:170341043
|
C | T | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2018-7108C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170341043 | ||||||
| chr6:170341098
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2018-7053C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170341098 | ||||||
| chr6:170341196
|
C | G | 11 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(8): Show | 11 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.2018-6955C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170341196 | ||||||
| chr6:170341272
|
C | A | 48 | a0001c0002t0001g0102a0001c0002t0010g0103a0002c0003t0001g0134others(45): Show | 49 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.2018-6879C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170341272 | ||||||
| chr6:170341335
|
C | T | 1 | a0001c0002t0029g0091 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2018-6816C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170341335 | ||||||
| chr6:170341514
|
C | T | 1 | a0001c0002t0007g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2018-6637C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170341514 | ||||||
| chr6:170341567
|
C | T | 1 | a0001c0002t0004g0034 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2018-6584C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170341567 | ||||||
| chr6:170341634
|
A | G | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2018-6517A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170341634 | ||||||
| chr6:170341644
|
T | C | 156 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(153): Show | 160 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.2018-6507T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170341644 | ||||||
| chr6:170341702
|
C | G | 5 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(2): Show | 6 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2018-6449C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170341702 | ||||||
| chr6:170341823
|
G | A | 6 | a0001c0002t0004g0104a0001c0002t0029g0091a0001c0008t0001g0098others(3): Show | 6 | HG02055.hp2 HG02886.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2018-6328G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170341823 | ||||||
| chr6:170341921
|
C | T | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2018-6230C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170341921 | ||||||
| chr6:170342012
|
G | A | 43 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(40): Show | 44 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(41): Show |
intron_variant | MODIFIER | c.2018-6139G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170342012 | ||||||
| chr6:170342034
|
A | G | 1 | a0001c0008t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2018-6117A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170342034 | ||||||
| chr6:170342106
|
A | G | 10 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0032others(7): Show | 10 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2018-6045A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170342106 | ||||||
| chr6:170342284
|
G | A | 15 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2018-5867G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170342284 | ||||||
| chr6:170342797
|
T | G | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018-5354T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170342797 | ||||||
| chr6:170342862
|
A | C | 40 | a0001c0002t0001g0001a0001c0002t0001g0046a0001c0002t0001g0047others(37): Show | 41 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(38): Show |
intron_variant | MODIFIER | c.2018-5289A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170342862 | ||||||
| chr6:170343049
|
C | A | 45 | a0001c0002t0001g0105a0002c0003t0002g0106a0002c0003t0002g0108others(42): Show | 46 | HG00558.hp2 HG00639.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.2018-5102C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170343049 | ||||||
| chr6:170343103
|
G | A | 56 | a0001c0001t0001g0011a0001c0001t0001g0207a0001c0001t0001g0227others(53): Show | 57 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2018-5048G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170343103 | ||||||
| chr6:170343146
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2018-5005A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170343146 | ||||||
| chr6:170343234
|
A | G | 8 | a0001c0002t0001g0102a0001c0002t0004g0104a0001c0002t0010g0103others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2018-4917A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170343234 | ||||||
| chr6:170343273
|
AAGCCTTT others(1198): Show |
A | 3 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0001g0043 | 3 | HG02965.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2018-4872_2018-366 others(4): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170343273 | |||||
| chr6:170343400
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2018-4751G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170343400 | ||||||
| chr6:170343493
|
A | G | 1 | a0001c0001t0002g0244 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2018-4658A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170343493 | ||||||
| chr6:170343500
|
A | G | 5 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(2): Show | 6 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2018-4651A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170343500 | ||||||
| chr6:170344047
|
ACTGGTTC others(169): Show |
A | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2018-4013_2018-383 others(4): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170344047 | |||||
| chr6:170344112
|
G | A | 24 | a0001c0002t0001g0105a0001c0002t0013g0039a0001c0002t0013g0040others(21): Show | 25 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.2018-4039G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344112 | ||||||
| chr6:170344120
|
C | G | 2 | a0001c0002t0001g0024a0001c0002t0001g0035 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2018-4031C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344120 | ||||||
| chr6:170344138
|
C | G | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2018-4013C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344138 | ||||||
| chr6:170344170
|
A | G | 3 | a0001c0002t0029g0091a0001c0008t0001g0098a0001c0008t0001g0099 | 3 | HG02886.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2018-3981A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344170 | ||||||
| chr6:170344223
|
T | A | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018-3928T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344223 | ||||||
| chr6:170344226
|
G | C | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2018-3925G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344226 | ||||||
| chr6:170344266
|
G | A | 1 | a0001c0001t0010g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2018-3885G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344266 | ||||||
| chr6:170344270
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2018-3881A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344270 | ||||||
| chr6:170344297
|
G | A | 1 | a0002c0003t0021g0113 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2018-3854G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344297 | ||||||
| chr6:170344310
|
C | CTCTGGTT others(81): Show |
1 | a0001c0001t0008g0197 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2018-3841_2018-384 others(92): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344310 | ||||||
| chr6:170344311
|
A | T | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2018-3840A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344311 | ||||||
| chr6:170344327
|
ACCCACCT others(169): Show |
A | 25 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0001g0105others(22): Show | 26 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2018-3723_2018-354 others(4): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170344327 | |||||
| chr6:170344354
|
G | A | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2018-3797G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344354 | ||||||
| chr6:170344364
|
T | G | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2018-3787T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344364 | ||||||
| chr6:170344399
|
T | TCTGGTTC others(81): Show |
1 | a0002c0003t0002g0136 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2018-3664_2018-357 others(92): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170344399 | |||||
| chr6:170344439
|
ATCGTTCA others(3): Show |
A | 1 | a0002c0003t0002g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2018-3711_2018-370 others(14): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344439 | ||||||
| chr6:170344441
|
C | T | 1 | a0002c0003t0002g0146 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2018-3710C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344441 | ||||||
| chr6:170344457
|
C | G | 4 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0241others(1): Show | 4 | HG01243.hp1 HG01891.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2018-3694C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344457 | ||||||
| chr6:170344560
|
C | T | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2018-3591C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344560 | ||||||
| chr6:170344648
|
A | G | 1 | a0001c0001t0006g0220 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2018-3503A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344648 | ||||||
| chr6:170344653
|
G | A | 47 | a0001c0001t0001g0247a0002c0003t0001g0134a0002c0003t0002g0004others(44): Show | 48 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.2018-3498G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344653 | ||||||
| chr6:170344659
|
C | T | 7 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2018-3492C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344659 | ||||||
| chr6:170344699
|
G | T | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2018-3452G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344699 | ||||||
| chr6:170344750
|
A | C | 1 | a0001c0001t0006g0209 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2018-3401A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344750 | ||||||
| chr6:170344793
|
T | C | 1 | a0001c0015t0001g0252 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2018-3358T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344793 | ||||||
| chr6:170344912
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2018-3239C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344912 | ||||||
| chr6:170344948
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2018-3203T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170344948 | ||||||
| chr6:170345031
|
C | T | 3 | a0001c0001t0005g0205a0001c0001t0005g0258a0001c0001t0020g0206 | 3 | HG01192.hp2 HG01934.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2018-3120C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170345031 | ||||||
| chr6:170345049
|
C | T | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2018-3102C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170345049 | ||||||
| chr6:170345157
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2018-2994A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170345157 | ||||||
| chr6:170345175
|
C | T | 46 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(43): Show | 48 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(45): Show |
intron_variant | MODIFIER | c.2018-2976C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170345175 | ||||||
| chr6:170345184
|
C | G | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2018-2967C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170345184 | ||||||
| chr6:170345315
|
T | G | 7 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2018-2836T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170345315 | ||||||
| chr6:170345332
|
G | T | 1 | a0002c0003t0002g0126 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2018-2819G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170345332 | ||||||
| chr6:170345524
|
G | A | 1 | a0001c0002t0001g0021 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2018-2627G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170345524 | ||||||
| chr6:170345569
|
C | T | 2 | a0004c0005t0001g0085a0004c0005t0001g0089 | 2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2018-2582C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170345569 | ||||||
| chr6:170345683
|
T | C | 57 | a0001c0001t0001g0011a0001c0001t0001g0207a0001c0001t0001g0227others(54): Show | 58 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.2018-2468T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170345683 | ||||||
| chr6:170345806
|
A | G | 259 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(256): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.2018-2345A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170345806 | ||||||
| chr6:170345908
|
A | G | 158 | a0001c0001t0010g0095a0001c0001t0010g0096a0001c0002t0001g0001others(155): Show | 162 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.2018-2243A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170345908 | ||||||
| chr6:170345923
|
A | G | 3 | a0001c0006t0001g0253a0001c0006t0001g0254a0001c0006t0001g0255 | 3 | NA18968.hp1 NA19085.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2018-2228A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170345923 | ||||||
| chr6:170345943
|
A | T | 2 | a0001c0009t0017g0093a0001c0009t0018g0092 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2018-2208A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170345943 | ||||||
| chr6:170346039
|
T | A | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2018-2112T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346039 | ||||||
| chr6:170346122
|
G | A | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2018-2029G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346122 | ||||||
| chr6:170346146
|
C | T | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2018-2005C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346146 | ||||||
| chr6:170346187
|
C | CTT | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2018-1954_2018-195 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170346187 | |||||
| chr6:170346187
|
CT | C | 46 | a0001c0001t0026g0223a0002c0003t0001g0134a0002c0003t0002g0004others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2018-1953delT | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 170346187 | |||||
| chr6:170346204
|
A | C | 34 | a0001c0001t0001g0207a0001c0001t0005g0171a0001c0001t0005g0205others(31): Show | 34 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.2018-1947A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346204 | ||||||
| chr6:170346254
|
A | G | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2018-1897A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346254 | ||||||
| chr6:170346255
|
T | TTCACCCC others(3): Show |
1 | a0002c0003t0002g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2018-1896_2018-189 others(14): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346255 | ||||||
| chr6:170346257
|
T | C | 1 | a0002c0003t0002g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2018-1894T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346257 | ||||||
| chr6:170346265
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2018-1886C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346265 | ||||||
| chr6:170346459
|
A | T | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2018-1692A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346459 | ||||||
| chr6:170346606
|
C | T | 12 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(9): Show | 12 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.2018-1545C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346606 | ||||||
| chr6:170346613
|
G | A | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2018-1538G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346613 | ||||||
| chr6:170346699
|
AT | A | 3 | a0001c0001t0005g0213a0001c0001t0005g0214a0001c0001t0005g0221 | 3 | HG00639.hp2 HG01109.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2018-1451delT | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346699 | ||||||
| chr6:170346768
|
G | C | 156 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(153): Show | 160 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.2018-1383G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346768 | ||||||
| chr6:170346792
|
G | A | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2018-1359G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346792 | ||||||
| chr6:170346813
|
C | A | 1 | a0002c0003t0002g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2018-1338C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346813 | ||||||
| chr6:170346813
|
C | T | 43 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(40): Show | 44 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(41): Show |
intron_variant | MODIFIER | c.2018-1338C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346813 | ||||||
| chr6:170346814
|
G | C | 1 | a0002c0003t0002g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2018-1337G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346814 | ||||||
| chr6:170346815
|
T | G | 1 | a0002c0003t0002g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2018-1336T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346815 | ||||||
| chr6:170346827
|
G | A | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2018-1324G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346827 | ||||||
| chr6:170346860
|
A | G | 3 | a0001c0001t0001g0245a0001c0001t0001g0250a0001c0001t0005g0249 | 3 | HG03471.hp1 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2018-1291A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346860 | ||||||
| chr6:170346927
|
G | T | 1 | a0002c0003t0002g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2018-1224G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170346927 | ||||||
| chr6:170347074
|
T | C | 1 | a0001c0002t0001g0060 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2018-1077T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170347074 | ||||||
| chr6:170347154
|
T | C | 36 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(33): Show | 36 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.2018-997T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170347154 | ||||||
| chr6:170347441
|
G | A | 1 | a0001c0001t0006g0201 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2018-710G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170347441 | ||||||
| chr6:170347857
|
G | C | 1 | a0001c0002t0001g0071 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2018-294G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170347857 | ||||||
| chr6:170347967
|
G | A | 1 | a0002c0003t0002g0136 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2018-184G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 4/10 | chr6 | 170347967 | ||||||
| chr6:170348384
|
T | G | 1 | a0002c0003t0002g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2190+61T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170348384 | ||||||
| chr6:170348476
|
A | G | 1 | a0003c0004t0003g0164 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2190+153A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170348476 | ||||||
| chr6:170348490
|
A | T | 5 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(2): Show | 6 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2190+167A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170348490 | ||||||
| chr6:170348505
|
C | G | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2190+182C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170348505 | ||||||
| chr6:170348605
|
A | G | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2190+282A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170348605 | ||||||
| chr6:170348697
|
G | T | 1 | a0001c0002t0004g0026 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2190+374G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170348697 | ||||||
| chr6:170348788
|
C | A | 1 | a0001c0002t0001g0044 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2190+465C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170348788 | ||||||
| chr6:170348830
|
A | T | 5 | a0001c0002t0029g0091a0001c0008t0001g0098a0001c0008t0001g0099others(2): Show | 5 | HG02886.hp1 HG03139.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2190+507A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170348830 | ||||||
| chr6:170348844
|
G | A | 5 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(2): Show | 6 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2190+521G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170348844 | ||||||
| chr6:170348868
|
G | A | 33 | a0001c0001t0001g0207a0001c0001t0005g0171a0001c0001t0005g0202others(30): Show | 33 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.2190+545G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170348868 | ||||||
| chr6:170349283
|
C | A | 2 | a0001c0009t0017g0093a0001c0009t0018g0092 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2190+960C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170349283 | ||||||
| chr6:170349330
|
T | TA | 3 | a0001c0002t0029g0091a0001c0008t0001g0098a0001c0008t0001g0099 | 3 | HG02886.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2190+1008dupA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 170349330 | |||||
| chr6:170349392
|
A | G | 1 | a0001c0002t0001g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2190+1069A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170349392 | ||||||
| chr6:170349433
|
C | A | 27 | a0001c0001t0001g0204a0001c0001t0001g0245a0001c0001t0001g0247others(24): Show | 27 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.2190+1110C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170349433 | ||||||
| chr6:170349505
|
C | A | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2190+1182C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170349505 | ||||||
| chr6:170349604
|
C | T | 3 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0001g0038 | 3 | HG02615.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2190+1281C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170349604 | ||||||
| chr6:170349696
|
A | T | 1 | a0002c0003t0002g0109 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2190+1373A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170349696 | ||||||
| chr6:170349749
|
C | T | 48 | a0001c0001t0005g0214a0001c0002t0004g0026a0002c0003t0001g0134others(45): Show | 49 | HG00099.hp2 HG00558.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.2190+1426C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170349749 | ||||||
| chr6:170349777
|
G | C | 9 | a0001c0002t0007g0006a0001c0002t0007g0007a0001c0002t0007g0008others(6): Show | 12 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.2190+1454G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170349777 | ||||||
| chr6:170349895
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2190+1572C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170349895 | ||||||
| chr6:170349989
|
C | T | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2190+1666C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170349989 | ||||||
| chr6:170350040
|
A | G | 23 | a0001c0001t0025g0187a0001c0002t0001g0105a0003c0004t0003g0005others(20): Show | 24 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.2190+1717A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170350040 | ||||||
| chr6:170350161
|
C | T | 1 | a0001c0002t0007g0008 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2190+1838C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170350161 | ||||||
| chr6:170350173
|
A | G | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2190+1850A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170350173 | ||||||
| chr6:170350280
|
G | A | 7 | a0004c0005t0001g0084a0004c0005t0001g0085a0004c0005t0001g0086others(4): Show | 7 | HG02723.hp2 HG02965.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2190+1957G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170350280 | ||||||
| chr6:170350339
|
G | A | 1 | a0001c0002t0010g0103 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2190+2016G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170350339 | ||||||
| chr6:170350632
|
T | C | 279 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(276): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.2190+2309T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170350632 | ||||||
| chr6:170350633
|
A | G | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2190+2310A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170350633 | ||||||
| chr6:170350661
|
A | G | 1 | a0002c0003t0002g0141 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2190+2338A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170350661 | ||||||
| chr6:170350707
|
G | A | 1 | a0005c0007t0012g0002 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2190+2384G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170350707 | ||||||
| chr6:170350744
|
CA | C | 76 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(73): Show | 78 | HG00099.hp1 HG00558.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.2190+2427delA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 170350744 | |||||
| chr6:170350806
|
C | G | 1 | a0001c0001t0001g0259 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2190+2483C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170350806 | ||||||
| chr6:170350876
|
C | T | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2190+2553C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170350876 | ||||||
| chr6:170350952
|
G | A | 1 | a0002c0003t0002g0117 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2190+2629G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170350952 | ||||||
| chr6:170351018
|
T | C | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2190+2695T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170351018 | ||||||
| chr6:170351175
|
T | C | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2190+2852T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170351175 | ||||||
| chr6:170351360
|
T | G | 1 | a0001c0001t0006g0209 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2190+3037T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170351360 | ||||||
| chr6:170351546
|
G | C | 2 | a0004c0005t0001g0085a0004c0005t0001g0089 | 2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2190+3223G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170351546 | ||||||
| chr6:170351619
|
A | C | 7 | a0004c0005t0001g0084a0004c0005t0001g0085a0004c0005t0001g0086others(4): Show | 7 | HG02723.hp2 HG02965.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2190+3296A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170351619 | ||||||
| chr6:170351637
|
A | G | 1 | a0006c0010t0010g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2190+3314A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170351637 | ||||||
| chr6:170351789
|
G | A | 1 | a0001c0002t0001g0051 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2190+3466G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170351789 | ||||||
| chr6:170351972
|
C | T | 1 | a0001c0001t0025g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2190+3649C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170351972 | ||||||
| chr6:170352258
|
C | T | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2190+3935C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170352258 | ||||||
| chr6:170352307
|
A | G | 2 | a0001c0001t0005g0202a0001c0001t0005g0225 | 2 | HG00735.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2190+3984A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170352307 | ||||||
| chr6:170352503
|
T | C | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2190+4180T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170352503 | ||||||
| chr6:170352524
|
G | A | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2190+4201G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170352524 | ||||||
| chr6:170352538
|
T | C | 2 | a0002c0003t0002g0133a0002c0003t0002g0135 | 2 | HG00673.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.2190+4215T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170352538 | ||||||
| chr6:170352804
|
C | G | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2190+4481C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170352804 | ||||||
| chr6:170352809
|
A | G | 15 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2190+4486A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170352809 | ||||||
| chr6:170352926
|
T | A | 1 | a0001c0002t0011g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2190+4603T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170352926 | ||||||
| chr6:170352936
|
T | C | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2190+4613T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170352936 | ||||||
| chr6:170352963
|
T | A | 1 | a0001c0018t0006g0215 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2190+4640T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170352963 | ||||||
| chr6:170353009
|
C | A | 1 | a0001c0002t0001g0065 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2190+4686C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170353009 | ||||||
| chr6:170353020
|
A | G | 1 | a0001c0002t0001g0035 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2190+4697A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170353020 | ||||||
| chr6:170353070
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2190+4747C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170353070 | ||||||
| chr6:170353160
|
T | C | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2190+4837T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170353160 | ||||||
| chr6:170353171
|
C | G | 1 | a0002c0003t0002g0137 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2190+4848C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170353171 | ||||||
| chr6:170353270
|
C | CAA | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2191-4948_2191-494 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 170353270 | |||||
| chr6:170353335
|
G | A | 2 | a0001c0002t0013g0039a0001c0002t0013g0040 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2191-4891G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170353335 | ||||||
| chr6:170353358
|
C | A | 2 | a0003c0004t0003g0159a0003c0004t0003g0160 | 2 | HG02056.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.2191-4868C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170353358 | ||||||
| chr6:170353444
|
C | G | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2191-4782C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170353444 | ||||||
| chr6:170353599
|
G | A | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2191-4627G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170353599 | ||||||
| chr6:170353841
|
A | G | 1 | a0001c0001t0010g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2191-4385A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170353841 | ||||||
| chr6:170354202
|
A | G | 8 | a0001c0002t0001g0102a0001c0002t0004g0104a0001c0002t0010g0103others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2191-4024A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170354202 | ||||||
| chr6:170354504
|
A | G | 1 | a0001c0002t0001g0056 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2191-3722A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170354504 | ||||||
| chr6:170354506
|
G | A | 10 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0032others(7): Show | 10 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2191-3720G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170354506 | ||||||
| chr6:170354649
|
C | T | 1 | a0001c0001t0006g0220 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2191-3577C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170354649 | ||||||
| chr6:170354650
|
G | A | 2 | a0001c0002t0013g0039a0001c0002t0013g0040 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2191-3576G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170354650 | ||||||
| chr6:170354747
|
C | T | 1 | a0002c0003t0002g0125 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2191-3479C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170354747 | ||||||
| chr6:170354768
|
GA | G | 156 | a0001c0001t0001g0261a0001c0001t0009g0278a0001c0002t0001g0001others(153): Show | 160 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.2191-3447delA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 170354768 | |||||
| chr6:170354877
|
C | T | 1 | a0001c0002t0001g0046 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2191-3349C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170354877 | ||||||
| chr6:170354878
|
G | A | 20 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(17): Show | 20 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.2191-3348G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170354878 | ||||||
| chr6:170354884
|
G | A | 1 | a0001c0001t0006g0175 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2191-3342G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170354884 | ||||||
| chr6:170354900
|
G | A | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2191-3326G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170354900 | ||||||
| chr6:170354912
|
G | A | 1 | a0002c0003t0002g0004 | 2 | HG00099.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2191-3314G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170354912 | ||||||
| chr6:170355013
|
A | G | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2191-3213A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170355013 | ||||||
| chr6:170355080
|
C | T | 77 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(74): Show | 79 | HG00099.hp1 HG00558.hp1 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.2191-3146C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170355080 | ||||||
| chr6:170355081
|
G | A | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2191-3145G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170355081 | ||||||
| chr6:170355240
|
C | G | 3 | a0001c0002t0029g0091a0001c0008t0001g0098a0001c0008t0001g0099 | 3 | HG02886.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2191-2986C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170355240 | ||||||
| chr6:170355246
|
A | G | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2191-2980A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170355246 | ||||||
| chr6:170355298
|
A | G | 2 | a0006c0010t0010g0019a0006c0010t0010g0020 | 2 | HG01099.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2191-2928A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170355298 | ||||||
| chr6:170355535
|
A | G | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2191-2691A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170355535 | ||||||
| chr6:170355670
|
G | A | 1 | a0002c0003t0002g0127 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2191-2556G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170355670 | ||||||
| chr6:170355843
|
C | T | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2191-2383C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170355843 | ||||||
| chr6:170356009
|
C | T | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2191-2217C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170356009 | ||||||
| chr6:170356127
|
A | G | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2191-2099A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170356127 | ||||||
| chr6:170356202
|
T | C | 36 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(33): Show | 36 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.2191-2024T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170356202 | ||||||
| chr6:170356345
|
C | T | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2191-1881C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170356345 | ||||||
| chr6:170356376
|
A | G | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2191-1850A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170356376 | ||||||
| chr6:170356404
|
G | A | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2191-1822G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170356404 | ||||||
| chr6:170356590
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2191-1636C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170356590 | ||||||
| chr6:170356992
|
C | T | 1 | a0003c0004t0003g0153 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2191-1234C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170356992 | ||||||
| chr6:170357159
|
C | T | 1 | a0001c0002t0004g0033 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2191-1067C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170357159 | ||||||
| chr6:170357161
|
C | T | 1 | a0002c0003t0002g0107 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2191-1065C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170357161 | ||||||
| chr6:170357242
|
AG | A | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2191-983delG | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170357242 | ||||||
| chr6:170357390
|
C | T | 3 | a0003c0004t0003g0168a0003c0004t0003g0169a0003c0004t0003g0170 | 3 | NA18944.hp1 NA18990.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2191-836C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170357390 | ||||||
| chr6:170357432
|
G | A | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2191-794G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170357432 | ||||||
| chr6:170357563
|
C | T | 1 | a0001c0001t0027g0210 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2191-663C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170357563 | ||||||
| chr6:170357564
|
G | A | 7 | a0004c0005t0001g0084a0004c0005t0001g0085a0004c0005t0001g0086others(4): Show | 7 | HG02723.hp2 HG02965.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2191-662G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170357564 | ||||||
| chr6:170357634
|
G | A | 1 | a0001c0001t0006g0172 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2191-592G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170357634 | ||||||
| chr6:170357707
|
C | G | 1 | a0002c0003t0002g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2191-519C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170357707 | ||||||
| chr6:170357799
|
C | T | 8 | a0001c0002t0001g0102a0001c0002t0004g0104a0001c0002t0010g0103others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2191-427C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170357799 | ||||||
| chr6:170357867
|
C | T | 1 | a0002c0003t0002g0108 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2191-359C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170357867 | ||||||
| chr6:170357892
|
T | C | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2191-334T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170357892 | ||||||
| chr6:170357994
|
CTG | C | 6 | a0003c0004t0003g0157a0003c0004t0003g0158a0003c0004t0003g0161others(3): Show | 6 | HG01978.hp2 HG02132.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.2191-224_2191-223d others(4): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 170357994 | |||||
| chr6:170358046
|
ATG | A | 6 | a0004c0005t0001g0084a0004c0005t0001g0085a0004c0005t0001g0086others(3): Show | 6 | HG02965.hp2 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2191-173_2191-172d others(4): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr6 | 170358046 | |||||
| chr6:170358201
|
A | G | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2191-25A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 5/10 | chr6 | 170358201 | ||||||
| chr6:170358442
|
C | T | 30 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(27): Show | 30 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2283+124C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170358442 | ||||||
| chr6:170358585
|
A | G | 27 | a0001c0001t0001g0204a0001c0001t0001g0245a0001c0001t0001g0247others(24): Show | 27 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.2283+267A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170358585 | ||||||
| chr6:170358676
|
G | C | 195 | a0001c0001t0001g0204a0001c0001t0001g0245a0001c0001t0001g0247others(192): Show | 199 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.2283+358G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170358676 | ||||||
| chr6:170358689
|
G | A | 1 | a0001c0001t0005g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2283+371G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170358689 | ||||||
| chr6:170358724
|
G | C | 156 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(153): Show | 160 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.2283+406G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170358724 | ||||||
| chr6:170358951
|
C | T | 4 | a0002c0003t0002g0107a0002c0003t0002g0110a0002c0003t0007g0112others(1): Show | 4 | HG02895.hp2 HG02896.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.2283+633C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170358951 | ||||||
| chr6:170359122
|
C | T | 1 | a0001c0002t0001g0075 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2283+804C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170359122 | ||||||
| chr6:170359229
|
C | T | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2283+911C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170359229 | ||||||
| chr6:170359302
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2283+984A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170359302 | ||||||
| chr6:170359380
|
C | A | 1 | a0001c0017t0001g0080 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2283+1062C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170359380 | ||||||
| chr6:170359393
|
C | CA | 38 | a0001c0001t0005g0171a0001c0001t0006g0172a0001c0001t0006g0173others(35): Show | 39 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.2283+1090dupA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170359393 | |||||
| chr6:170359393
|
CA | C | 72 | a0001c0001t0001g0245a0001c0001t0001g0247a0001c0001t0001g0248others(69): Show | 73 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.2283+1090delA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170359393 | |||||
| chr6:170359413
|
C | G | 9 | a0001c0002t0007g0006a0001c0002t0007g0007a0001c0002t0007g0008others(6): Show | 12 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.2283+1095C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170359413 | ||||||
| chr6:170359464
|
G | A | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2283+1146G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170359464 | ||||||
| chr6:170359604
|
G | A | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2283+1286G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170359604 | ||||||
| chr6:170359635
|
C | T | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2283+1317C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170359635 | ||||||
| chr6:170359675
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2283+1357G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170359675 | ||||||
| chr6:170359683
|
C | T | 1 | a0004c0005t0009g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2283+1365C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170359683 | ||||||
| chr6:170359708
|
G | A | 2 | a0001c0002t0011g0016a0001c0002t0011g0017 | 2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2283+1390G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170359708 | ||||||
| chr6:170359734
|
C | T | 8 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0025others(5): Show | 8 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2283+1416C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170359734 | ||||||
| chr6:170359793
|
C | T | 1 | a0001c0002t0001g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2283+1475C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170359793 | ||||||
| chr6:170359804
|
C | T | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2283+1486C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170359804 | ||||||
| chr6:170359883
|
A | C | 2 | a0001c0001t0016g0198a0001c0001t0016g0199 | 2 | HG01123.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.2283+1565A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170359883 | ||||||
| chr6:170359917
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2283+1599C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170359917 | ||||||
| chr6:170360065
|
C | G | 7 | a0001c0001t0001g0229a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG02572.hp2 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2283+1747C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170360065 | ||||||
| chr6:170360143
|
G | A | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2283+1825G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170360143 | ||||||
| chr6:170360243
|
G | A | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2283+1925G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170360243 | ||||||
| chr6:170360328
|
C | CAACA | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2283+2010_2283+201 others(8): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170360328 | ||||||
| chr6:170360352
|
A | G | 157 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(154): Show | 161 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.2283+2034A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170360352 | ||||||
| chr6:170360543
|
C | T | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2283+2225C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170360543 | ||||||
| chr6:170360555
|
A | G | 1 | a0001c0001t0025g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2283+2237A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170360555 | ||||||
| chr6:170360578
|
A | T | 1 | a0001c0001t0006g0209 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2283+2260A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170360578 | ||||||
| chr6:170360693
|
G | T | 1 | a0001c0001t0001g0238 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2283+2375G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170360693 | ||||||
| chr6:170360786
|
G | C | 6 | a0001c0002t0004g0104a0001c0002t0029g0091a0001c0008t0001g0098others(3): Show | 6 | HG02055.hp2 HG02886.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2283+2468G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170360786 | ||||||
| chr6:170360805
|
T | C | 154 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(151): Show | 158 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.2283+2487T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170360805 | ||||||
| chr6:170360846
|
T | A | 44 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(41): Show | 45 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(42): Show |
intron_variant | MODIFIER | c.2283+2528T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170360846 | ||||||
| chr6:170360882
|
C | T | 1 | a0001c0002t0001g0075 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2283+2564C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170360882 | ||||||
| chr6:170360899
|
A | G | 9 | a0001c0002t0007g0006a0001c0002t0007g0007a0001c0002t0007g0008others(6): Show | 12 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.2283+2581A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170360899 | ||||||
| chr6:170361182
|
C | CTA | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02572.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2283+2875_2283+287 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361182 | |||||
| chr6:170361182
|
C | CTATATAT others(3): Show |
3 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0241 | 3 | HG01891.hp1 HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2283+2867_2283+287 others(14): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361182 | |||||
| chr6:170361182
|
C | CTATATAT others(5): Show |
7 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(4): Show | 7 | HG00280.hp2 HG01074.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.2283+2865_2283+287 others(16): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361182 | |||||
| chr6:170361182
|
C | CTATATAT others(11): Show |
3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2283+2877_2283+287 others(22): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361182 | |||||
| chr6:170361182
|
CTATATAT others(53): Show |
C | 2 | a0001c0001t0005g0217a0001c0001t0005g0218 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2283+2891_2283+295 others(64): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361182 | |||||
| chr6:170361193
|
T | TATATATA others(19): Show |
1 | a0003c0004t0003g0162 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2283+2876_2283+287 others(30): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361193 | |||||
| chr6:170361194
|
ACG | A | 3 | a0001c0002t0001g0105a0003c0004t0003g0157a0003c0004t0003g0158 | 3 | HG00639.hp1 NA18970.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.2283+2877_2283+287 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361194 | ||||||
| chr6:170361194
|
ACGTG | A | 13 | a0003c0004t0003g0152a0003c0004t0003g0153a0003c0004t0003g0154others(10): Show | 13 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.2283+2877_2283+288 others(8): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361194 | ||||||
| chr6:170361195
|
C | CGT | 2 | a0001c0001t0001g0011a0001c0001t0001g0240 | 3 | HG02280.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2283+2880_2283+288 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361195 | |||||
| chr6:170361195
|
C | T | 6 | a0003c0004t0003g0005a0003c0004t0003g0156a0003c0004t0003g0167others(3): Show | 7 | HG03225.hp1 NA18942.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.2283+2877C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361195 | ||||||
| chr6:170361196
|
G | A | 47 | a0001c0002t0001g0001a0001c0002t0001g0037a0001c0002t0001g0047others(44): Show | 49 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(46): Show |
intron_variant | MODIFIER | c.2283+2878G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361196 | ||||||
| chr6:170361198
|
G | A | 84 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(81): Show | 86 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.2283+2880G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361198 | ||||||
| chr6:170361198
|
G | GTA | 13 | a0001c0001t0001g0231a0001c0001t0001g0238a0001c0001t0001g0245others(10): Show | 13 | HG00642.hp1 HG00735.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2283+2917_2283+291 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361198 | |||||
| chr6:170361198
|
G | GTATA | 25 | a0001c0001t0001g0207a0001c0001t0001g0228a0001c0001t0001g0232others(22): Show | 26 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.2283+2915_2283+291 others(8): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361198 | |||||
| chr6:170361198
|
G | GTATATA | 13 | a0001c0001t0001g0229a0001c0001t0001g0235a0001c0001t0001g0236others(10): Show | 13 | HG00280.hp1 HG00741.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.2283+2913_2283+291 others(10): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361198 | |||||
| chr6:170361198
|
G | GTATATAT others(1): Show |
8 | a0001c0001t0001g0230a0001c0001t0001g0264a0001c0001t0001g0268others(5): Show | 10 | HG01256.hp2 HG01258.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.2283+2911_2283+291 others(12): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361198 | |||||
| chr6:170361198
|
G | GTATATAT others(3): Show |
3 | a0001c0001t0001g0227a0001c0001t0001g0262a0008c0016t0008g0196 | 3 | HG02155.hp2 HG02723.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2283+2909_2283+291 others(14): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361198 | |||||
| chr6:170361198
|
GTA | G | 9 | a0001c0001t0005g0205a0001c0001t0005g0214a0001c0001t0006g0173others(6): Show | 10 | HG00639.hp2 HG01099.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2283+2917_2283+291 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361198 | |||||
| chr6:170361198
|
GTATA | G | 4 | a0001c0001t0001g0272a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 4 | HG02572.hp2 HG02602.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2283+2915_2283+291 others(8): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361198 | |||||
| chr6:170361198
|
GTATATAT others(5): Show |
G | 1 | a0001c0001t0001g0204 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2283+2907_2283+291 others(16): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361198 | |||||
| chr6:170361198
|
GTATATAT others(11): Show |
G | 5 | a0001c0001t0008g0194a0001c0001t0008g0195a0001c0001t0008g0197others(2): Show | 5 | HG02015.hp1 HG02129.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.2283+2901_2283+291 others(22): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361198 | |||||
| chr6:170361200
|
A | G | 5 | a0001c0001t0001g0239a0001c0002t0001g0102a0001c0002t0010g0103others(2): Show | 5 | HG02559.hp1 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2283+2882A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361200 | ||||||
| chr6:170361202
|
A | ATATATAT others(7): Show |
2 | a0001c0002t0001g0070a0001c0002t0001g0071 | 2 | NA18971.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2283+2894_2283+289 others(18): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361202 | |||||
| chr6:170361202
|
A | G | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2283+2884A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361202 | ||||||
| chr6:170361203
|
T | C | 2 | a0001c0015t0001g0252a0003c0004t0003g0161 | 2 | HG01192.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.2283+2885T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361203 | ||||||
| chr6:170361204
|
A | ATATATAC others(3): Show |
1 | a0001c0002t0001g0064 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2283+2892_2283+289 others(14): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361204 | |||||
| chr6:170361204
|
A | ATATATAT others(3): Show |
1 | a0001c0002t0001g0055 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2283+2894_2283+289 others(14): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361204 | |||||
| chr6:170361204
|
A | ATATATAT others(5): Show |
29 | a0001c0002t0001g0001a0001c0002t0001g0051a0001c0002t0001g0053others(26): Show | 30 | HG00558.hp1 HG00673.hp1 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.2283+2894_2283+289 others(16): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361204 | |||||
| chr6:170361204
|
A | G | 32 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(29): Show | 32 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.2283+2886A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361204 | ||||||
| chr6:170361205
|
T | C | 2 | a0001c0001t0001g0257a0003c0004t0003g0161 | 2 | HG01496.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.2283+2887T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361205 | ||||||
| chr6:170361206
|
A | ATATATAC others(3): Show |
1 | a0001c0002t0001g0078 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2283+2894_2283+289 others(14): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361206 | |||||
| chr6:170361206
|
A | ATATATAC others(41): Show |
4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0048others(1): Show | 4 | NA18952.hp2 NA19068.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.2283+2894_2283+289 others(52): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361206 | |||||
| chr6:170361206
|
A | ATATATAC others(59): Show |
1 | a0001c0002t0001g0050 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2283+2894_2283+289 others(70): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361206 | |||||
| chr6:170361206
|
A | G | 2 | a0001c0001t0001g0257a0001c0015t0001g0252 | 2 | HG01192.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2283+2888A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361206 | ||||||
| chr6:170361208
|
A | ATATACGT others(39): Show |
1 | a0001c0002t0004g0069 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2283+2894_2283+289 others(50): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361208 | |||||
| chr6:170361208
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2283+2890A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361208 | ||||||
| chr6:170361210
|
A | ATG | 4 | a0004c0005t0001g0084a0004c0005t0001g0085a0004c0005t0001g0088others(1): Show | 4 | HG03098.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2283+2893_2283+289 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361210 | |||||
| chr6:170361212
|
A | G | 1 | a0004c0005t0001g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2283+2894A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361212 | ||||||
| chr6:170361214
|
A | ATACGTG | 4 | a0001c0002t0001g0021a0001c0002t0001g0024a0006c0010t0010g0019others(1): Show | 4 | HG01099.hp1 HG02818.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2283+2898_2283+289 others(10): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361214 | |||||
| chr6:170361214
|
A | G | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2283+2896A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361214 | ||||||
| chr6:170361215
|
T | C | 3 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0001g0038 | 3 | HG02615.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2283+2897T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361215 | ||||||
| chr6:170361216
|
A | ACG | 8 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(5): Show | 8 | HG02132.hp1 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2283+2898_2283+289 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361216 | ||||||
| chr6:170361216
|
A | ACGTG | 19 | a0001c0002t0001g0015a0001c0002t0001g0031a0001c0002t0001g0032others(16): Show | 19 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.2283+2898_2283+289 others(8): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361216 | ||||||
| chr6:170361216
|
A | ATACGTAT others(57): Show |
2 | a0001c0002t0013g0039a0001c0002t0013g0040 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2283+2900_2283+290 others(68): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361216 | |||||
| chr6:170361216
|
A | G | 3 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0001g0038 | 3 | HG02615.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2283+2898A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361216 | ||||||
| chr6:170361217
|
T | C | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2283+2899T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361217 | ||||||
| chr6:170361217
|
TATATATA others(13): Show |
T | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2283+2901_2283+292 others(24): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361217 | |||||
| chr6:170361218
|
A | G | 14 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(11): Show | 15 | HG02055.hp1 HG02132.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.2283+2900A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361218 | ||||||
| chr6:170361218
|
ATATATAT others(15): Show |
A | 1 | a0001c0002t0030g0182 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2283+2915_2283+293 others(26): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361218 | |||||
| chr6:170361219
|
T | C | 5 | a0002c0003t0002g0107a0002c0003t0002g0110a0002c0003t0002g0128others(2): Show | 5 | HG01256.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2283+2901T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361219 | ||||||
| chr6:170361219
|
TATATATA others(11): Show |
T | 1 | a0002c0003t0002g0115 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2283+2903_2283+292 others(22): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361219 | |||||
| chr6:170361220
|
A | ATATATAC others(3): Show |
1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2283+2908_2283+290 others(14): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361220 | |||||
| chr6:170361220
|
A | ATATATAT others(29): Show |
1 | a0004c0005t0001g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2283+2916_2283+291 others(40): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361220 | |||||
| chr6:170361220
|
A | G | 1 | a0002c0003t0002g0128 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2283+2902A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361220 | ||||||
| chr6:170361221
|
T | C | 44 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(41): Show | 45 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.2283+2903T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361221 | ||||||
| chr6:170361222
|
A | ACG | 38 | a0001c0002t0001g0001a0001c0002t0001g0046a0001c0002t0001g0047others(35): Show | 39 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(36): Show |
intron_variant | MODIFIER | c.2283+2904_2283+290 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361222 | ||||||
| chr6:170361222
|
A | ATATATAC others(45): Show |
1 | a0001c0002t0029g0091 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2283+2910_2283+291 others(56): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361222 | |||||
| chr6:170361222
|
A | ATATATAT others(7): Show |
2 | a0001c0008t0001g0098a0001c0008t0001g0099 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2283+2914_2283+291 others(18): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361222 | |||||
| chr6:170361222
|
A | G | 45 | a0001c0002t0001g0102a0002c0003t0001g0134a0002c0003t0002g0004others(42): Show | 46 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.2283+2904A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361222 | ||||||
| chr6:170361223
|
T | C | 1 | a0003c0004t0003g0153 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2283+2905T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361223 | ||||||
| chr6:170361224
|
A | G | 2 | a0001c0002t0010g0103a0002c0003t0002g0124 | 2 | HG02809.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2283+2906A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361224 | ||||||
| chr6:170361225
|
T | C | 1 | a0003c0004t0003g0153 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2283+2907T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361225 | ||||||
| chr6:170361227
|
T | C | 14 | a0001c0001t0016g0198a0003c0004t0003g0005a0003c0004t0003g0152others(11): Show | 15 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2283+2909T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361227 | ||||||
| chr6:170361229
|
T | C | 18 | a0001c0001t0016g0198a0003c0004t0003g0005a0003c0004t0003g0152others(15): Show | 19 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2283+2911T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361229 | ||||||
| chr6:170361230
|
A | G | 1 | a0001c0001t0016g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2283+2912A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361230 | ||||||
| chr6:170361231
|
T | C | 3 | a0003c0004t0003g0165a0003c0004t0003g0166a0003c0004t0003g0167 | 3 | NA18979.hp2 NA18982.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.2283+2913T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361231 | ||||||
| chr6:170361233
|
T | C | 1 | a0003c0004t0003g0162 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2283+2915T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361233 | ||||||
| chr6:170361234
|
ATACACGT others(17): Show |
A | 1 | a0003c0004t0003g0161 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2283+2919_2283+294 others(28): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361234 | |||||
| chr6:170361235
|
T | C | 2 | a0001c0001t0005g0219a0003c0004t0003g0162 | 2 | HG01943.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.2283+2917T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361235 | ||||||
| chr6:170361235
|
T | TATATATA others(3): Show |
1 | a0001c0001t0008g0010 | 2 | NA18952.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2283+2918_2283+291 others(14): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361235 | |||||
| chr6:170361235
|
TAC | T | 44 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(41): Show | 45 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.2283+2920_2283+292 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361235 | |||||
| chr6:170361237
|
C | CACACGTA others(35): Show |
1 | a0004c0005t0001g0084 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2283+2921_2283+292 others(46): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361237 | |||||
| chr6:170361237
|
C | T | 99 | a0001c0001t0010g0083a0001c0002t0001g0001a0001c0002t0001g0012others(96): Show | 101 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.2283+2919C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361237 | ||||||
| chr6:170361238
|
A | G | 4 | a0001c0002t0001g0102a0001c0002t0001g0105a0001c0002t0013g0039others(1): Show | 4 | HG00639.hp1 HG01891.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2283+2920A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361238 | ||||||
| chr6:170361239
|
C | T | 21 | a0001c0002t0001g0102a0001c0002t0001g0105a0001c0002t0013g0039others(18): Show | 22 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.2283+2921C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361239 | ||||||
| chr6:170361240
|
G | A | 21 | a0001c0002t0001g0102a0001c0002t0001g0105a0003c0004t0003g0005others(18): Show | 22 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.2283+2922G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361240 | ||||||
| chr6:170361240
|
GTA | G | 5 | a0001c0002t0001g0036a0001c0002t0004g0104a0001c0002t0029g0091others(2): Show | 5 | HG02055.hp2 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2283+2935_2283+293 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361240 | |||||
| chr6:170361242
|
A | ATATATAT others(77): Show |
1 | a0001c0001t0010g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2283+2934_2283+293 others(88): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361242 | |||||
| chr6:170361242
|
A | ATATATAT others(31): Show |
4 | a0004c0005t0001g0085a0004c0005t0001g0086a0004c0005t0001g0088others(1): Show | 4 | HG02965.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2283+2937_2283+293 others(42): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361242 | |||||
| chr6:170361242
|
A | ATATATAT others(7): Show |
1 | a0001c0002t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2283+2926_2283+293 others(18): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361242 | |||||
| chr6:170361242
|
A | ATATATAT others(9): Show |
3 | a0001c0002t0001g0037a0001c0002t0001g0038a0001c0002t0010g0103 | 3 | HG02615.hp2 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2283+2936_2283+293 others(20): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361242 | |||||
| chr6:170361242
|
A | ATATATAT others(27): Show |
1 | a0001c0009t0018g0092 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2283+2936_2283+293 others(38): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361242 | |||||
| chr6:170361242
|
A | ATATATAT others(29): Show |
1 | a0001c0009t0017g0093 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2283+2936_2283+293 others(40): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361242 | |||||
| chr6:170361242
|
A | G | 4 | a0001c0001t0010g0095a0001c0001t0010g0096a0004c0005t0001g0084others(1): Show | 4 | HG02717.hp1 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2283+2924A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361242 | ||||||
| chr6:170361253
|
T | C | 16 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(13): Show | 17 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2283+2935T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361253 | ||||||
| chr6:170361253
|
T | TATATATA others(3): Show |
2 | a0003c0004t0003g0156a0003c0004t0003g0169 | 2 | NA19060.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2283+2936_2283+293 others(14): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170361253 | |||||
| chr6:170361255
|
C | CAT | 3 | a0001c0002t0004g0026a0003c0004t0003g0162a0003c0004t0003g0167 | 3 | HG01167.hp1 NA18969.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2283+2937_2283+293 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361255 | ||||||
| chr6:170361255
|
C | T | 18 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(15): Show | 19 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2283+2937C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361255 | ||||||
| chr6:170361256
|
G | A | 51 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(48): Show | 52 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.2283+2938G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361256 | ||||||
| chr6:170361258
|
G | A | 153 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(150): Show | 157 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.2283+2940G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361258 | ||||||
| chr6:170361337
|
A | T | 1 | a0001c0001t0001g0231 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2283+3019A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361337 | ||||||
| chr6:170361449
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2283+3131G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361449 | ||||||
| chr6:170361511
|
G | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG00280.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2283+3193G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361511 | ||||||
| chr6:170361686
|
T | C | 1 | a0003c0004t0003g0163 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2283+3368T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361686 | ||||||
| chr6:170361690
|
C | T | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2283+3372C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361690 | ||||||
| chr6:170361729
|
G | A | 47 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(44): Show | 49 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(46): Show |
intron_variant | MODIFIER | c.2283+3411G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361729 | ||||||
| chr6:170361791
|
A | G | 1 | a0001c0001t0006g0172 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2283+3473A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361791 | ||||||
| chr6:170361845
|
G | A | 1 | a0001c0002t0001g0060 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2283+3527G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361845 | ||||||
| chr6:170361874
|
A | G | 3 | a0001c0001t0005g0205a0001c0001t0005g0258a0001c0001t0020g0206 | 3 | HG01192.hp2 HG01934.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2283+3556A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361874 | ||||||
| chr6:170361880
|
A | C | 1 | a0001c0001t0001g0272 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2283+3562A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361880 | ||||||
| chr6:170361887
|
G | T | 1 | a0001c0001t0001g0233 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2283+3569G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361887 | ||||||
| chr6:170361923
|
A | G | 1 | a0001c0002t0004g0033 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2283+3605A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170361923 | ||||||
| chr6:170362187
|
A | T | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2283+3869A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170362187 | ||||||
| chr6:170362195
|
G | T | 1 | a0001c0001t0006g0177 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2283+3877G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170362195 | ||||||
| chr6:170362374
|
G | A | 1 | a0001c0002t0001g0047 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2283+4056G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170362374 | ||||||
| chr6:170362384
|
T | C | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2283+4066T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170362384 | ||||||
| chr6:170362455
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2283+4137C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170362455 | ||||||
| chr6:170362460
|
G | A | 1 | a0001c0002t0001g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2283+4142G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170362460 | ||||||
| chr6:170362499
|
A | G | 35 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(32): Show | 35 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.2283+4181A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170362499 | ||||||
| chr6:170362559
|
T | A | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2283+4241T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170362559 | ||||||
| chr6:170362668
|
G | C | 2 | a0001c0002t0001g0102a0001c0002t0010g0103 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2283+4350G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170362668 | ||||||
| chr6:170362684
|
C | CT | 6 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(3): Show | 7 | HG00639.hp1 HG01109.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2283+4381dupT | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170362684 | |||||
| chr6:170362904
|
C | T | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2283+4586C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170362904 | ||||||
| chr6:170363100
|
A | G | 6 | a0001c0002t0004g0104a0001c0002t0029g0091a0001c0008t0001g0098others(3): Show | 6 | HG02055.hp2 HG02886.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2283+4782A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170363100 | ||||||
| chr6:170363220
|
T | C | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2283+4902T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170363220 | ||||||
| chr6:170363242
|
A | G | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2283+4924A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170363242 | ||||||
| chr6:170363699
|
G | A | 1 | a0001c0002t0001g0076 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2283+5381G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170363699 | ||||||
| chr6:170363805
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0190a0001c0001t0009g0191 | 4 | HG01109.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2283+5487C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170363805 | ||||||
| chr6:170364003
|
G | C | 34 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(31): Show | 34 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.2283+5685G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170364003 | ||||||
| chr6:170364048
|
A | T | 1 | a0003c0004t0003g0162 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2283+5730A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170364048 | ||||||
| chr6:170364155
|
G | T | 3 | a0001c0002t0004g0178a0001c0002t0004g0179a0001c0002t0004g0180 | 3 | HG00642.hp1 HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.2283+5837G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170364155 | ||||||
| chr6:170364424
|
T | C | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2283+6106T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170364424 | ||||||
| chr6:170364493
|
A | G | 8 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(5): Show | 8 | HG02280.hp1 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2283+6175A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170364493 | ||||||
| chr6:170364915
|
C | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG00280.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2283+6597C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170364915 | ||||||
| chr6:170364930
|
C | A | 1 | a0001c0002t0001g0079 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2283+6612C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170364930 | ||||||
| chr6:170364951
|
AT | A | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2283+6637delT | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170364951 | |||||
| chr6:170365062
|
G | A | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2283+6744G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170365062 | ||||||
| chr6:170365074
|
G | A | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2283+6756G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170365074 | ||||||
| chr6:170365102
|
T | G | 1 | a0004c0005t0001g0084 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2283+6784T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170365102 | ||||||
| chr6:170365249
|
A | G | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2283+6931A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170365249 | ||||||
| chr6:170365253
|
C | T | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2283+6935C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170365253 | ||||||
| chr6:170365278
|
T | C | 168 | a0001c0001t0010g0083a0001c0001t0010g0095a0001c0001t0010g0096others(165): Show | 172 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.2283+6960T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170365278 | ||||||
| chr6:170365578
|
A | G | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2283+7260A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170365578 | ||||||
| chr6:170365688
|
T | C | 156 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(153): Show | 160 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.2283+7370T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170365688 | ||||||
| chr6:170365696
|
C | A | 1 | a0001c0001t0027g0210 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2283+7378C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170365696 | ||||||
| chr6:170365714
|
T | TC | 16 | a0001c0001t0001g0232a0001c0001t0001g0270a0001c0001t0005g0171others(13): Show | 16 | HG00738.hp1 HG01099.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.2283+7404dupC | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170365714 | |||||
| chr6:170365715
|
C | A | 10 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0032others(7): Show | 10 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2283+7397C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170365715 | ||||||
| chr6:170365720
|
C | G | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2283+7402C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170365720 | ||||||
| chr6:170365829
|
C | T | 1 | a0001c0002t0007g0184 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2283+7511C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170365829 | ||||||
| chr6:170365854
|
A | G | 5 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2283+7536A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170365854 | ||||||
| chr6:170365884
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2283+7566C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170365884 | ||||||
| chr6:170365885
|
G | A | 5 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(2): Show | 6 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2283+7567G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170365885 | ||||||
| chr6:170365929
|
A | T | 1 | a0001c0002t0001g0070 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2283+7611A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170365929 | ||||||
| chr6:170365938
|
T | C | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2283+7620T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170365938 | ||||||
| chr6:170366015
|
T | A | 1 | a0001c0008t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2283+7697T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170366015 | ||||||
| chr6:170366052
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2283+7734G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170366052 | ||||||
| chr6:170366182
|
C | T | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2283+7864C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170366182 | ||||||
| chr6:170366303
|
G | C | 1 | a0001c0002t0030g0182 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2283+7985G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170366303 | ||||||
| chr6:170366328
|
G | C | 6 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(3): Show | 6 | HG00280.hp2 HG01074.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.2283+8010G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170366328 | ||||||
| chr6:170366354
|
C | T | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2283+8036C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170366354 | ||||||
| chr6:170366405
|
G | C | 11 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(8): Show | 11 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.2283+8087G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170366405 | ||||||
| chr6:170366448
|
A | G | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2283+8130A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170366448 | ||||||
| chr6:170366766
|
C | T | 6 | a0001c0002t0004g0104a0001c0002t0029g0091a0001c0008t0001g0098others(3): Show | 6 | HG02055.hp2 HG02886.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2283+8448C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170366766 | ||||||
| chr6:170366925
|
T | A | 89 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(86): Show | 90 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.2283+8607T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170366925 | ||||||
| chr6:170367238
|
C | A | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2283+8920C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170367238 | ||||||
| chr6:170367252
|
T | C | 1 | a0001c0001t0006g0172 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2283+8934T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170367252 | ||||||
| chr6:170367264
|
G | A | 10 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(7): Show | 11 | HG01123.hp1 HG01243.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.2283+8946G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170367264 | ||||||
| chr6:170367281
|
C | T | 13 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(10): Show | 13 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.2283+8963C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170367281 | ||||||
| chr6:170367282
|
G | A | 1 | a0001c0002t0001g0055 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2283+8964G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170367282 | ||||||
| chr6:170367312
|
A | G | 1 | a0001c0002t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2283+8994A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170367312 | ||||||
| chr6:170367387
|
A | C | 1 | a0001c0002t0010g0103 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2283+9069A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170367387 | ||||||
| chr6:170367389
|
C | T | 1 | a0001c0001t0027g0210 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2283+9071C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170367389 | ||||||
| chr6:170367643
|
G | T | 9 | a0001c0002t0007g0006a0001c0002t0007g0007a0001c0002t0007g0008others(6): Show | 12 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.2283+9325G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170367643 | ||||||
| chr6:170367793
|
T | C | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2283+9475T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170367793 | ||||||
| chr6:170367996
|
T | C | 7 | a0001c0001t0010g0083a0004c0005t0001g0084a0004c0005t0001g0085others(4): Show | 7 | HG02965.hp2 HG03041.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2283+9678T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170367996 | ||||||
| chr6:170368217
|
G | C | 1 | a0001c0008t0001g0098 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2283+9899G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368217 | ||||||
| chr6:170368218
|
G | C | 1 | a0001c0002t0004g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2283+9900G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368218 | ||||||
| chr6:170368242
|
C | T | 5 | a0001c0001t0005g0171a0001c0001t0006g0173a0001c0001t0006g0175others(2): Show | 5 | HG01175.hp1 HG01361.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.2283+9924C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368242 | ||||||
| chr6:170368289
|
T | C | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2283+9971T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368289 | ||||||
| chr6:170368368
|
CCTT | C | 7 | a0001c0001t0010g0083a0004c0005t0001g0084a0004c0005t0001g0085others(4): Show | 7 | HG02965.hp2 HG03041.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2283+10053_2283+10 others(9): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170368368 | |||||
| chr6:170368502
|
G | A | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2283+10184G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368502 | ||||||
| chr6:170368549
|
T | C | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG00280.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2283+10231T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368549 | ||||||
| chr6:170368649
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2283+10331C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368649 | ||||||
| chr6:170368651
|
C | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0190a0001c0001t0009g0191 | 4 | HG01109.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2283+10333C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368651 | ||||||
| chr6:170368742
|
A | G | 1 | a0001c0001t0006g0172 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2283+10424A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368742 | ||||||
| chr6:170368744
|
A | G | 1 | a0001c0002t0001g0037 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2283+10426A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368744 | ||||||
| chr6:170368818
|
G | GC | 3 | a0001c0002t0010g0103a0001c0002t0013g0039a0001c0002t0013g0040 | 3 | HG01891.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2283+10501dupC | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170368818 | |||||
| chr6:170368818
|
GCTGGGGG others(12): Show |
G | 1 | a0001c0001t0008g0194 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2283+10505_2283+10 others(25): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170368818 | |||||
| chr6:170368819
|
C | CG | 5 | a0001c0002t0029g0091a0001c0008t0001g0098a0001c0008t0001g0099others(2): Show | 5 | HG01099.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2283+10501_2283+10 others(7): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368819 | ||||||
| chr6:170368819
|
C | CGG | 13 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0015others(10): Show | 13 | HG01069.hp2 HG01167.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2283+10501_2283+10 others(8): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368819 | ||||||
| chr6:170368819
|
C | CGGG | 8 | a0001c0002t0001g0014a0001c0002t0001g0024a0001c0002t0001g0035others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2283+10501_2283+10 others(9): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368819 | ||||||
| chr6:170368819
|
CTG | C | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2283+10502_2283+10 others(8): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368819 | ||||||
| chr6:170368820
|
T | G | 146 | a0001c0001t0010g0083a0001c0001t0010g0095a0001c0001t0010g0096others(143): Show | 149 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.2283+10502T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368820 | ||||||
| chr6:170368820
|
T | TG | 57 | a0001c0001t0001g0011a0001c0001t0001g0207a0001c0001t0001g0227others(54): Show | 59 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.2283+10512dupG | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170368820 | |||||
| chr6:170368820
|
T | TGG | 29 | a0001c0001t0001g0232a0001c0001t0001g0245a0001c0001t0001g0247others(26): Show | 29 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2283+10511_2283+10 others(8): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170368820 | |||||
| chr6:170368820
|
TG | T | 18 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0195others(15): Show | 22 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2283+10512delG | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170368820 | |||||
| chr6:170368822
|
G | GT | 8 | a0001c0001t0010g0083a0001c0002t0004g0104a0004c0005t0001g0084others(5): Show | 8 | HG02055.hp2 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.2283+10504_2283+10 others(7): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368822 | ||||||
| chr6:170368823
|
G | GA | 3 | a0001c0001t0001g0204a0001c0001t0006g0256a0001c0018t0006g0215 | 3 | HG02738.hp1 HG02738.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.2283+10505_2283+10 others(7): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368823 | ||||||
| chr6:170368823
|
G | GC | 49 | a0001c0002t0001g0102a0001c0009t0017g0093a0001c0009t0018g0092others(46): Show | 50 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.2283+10505_2283+10 others(7): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368823 | ||||||
| chr6:170368824
|
G | C | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2283+10506G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368824 | ||||||
| chr6:170368824
|
G | GT | 42 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(39): Show | 43 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(40): Show |
intron_variant | MODIFIER | c.2283+10506_2283+10 others(7): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368824 | ||||||
| chr6:170368950
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2283+10632G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170368950 | ||||||
| chr6:170368995
|
T | TTGGGGAT others(125): Show |
20 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(17): Show | 21 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2283+10678_2283+10 others(138): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170368995 | |||||
| chr6:170369072
|
G | GTTTTACT others(125): Show |
1 | a0003c0004t0003g0158 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2283+10809_2283+10 others(138): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170369072 | |||||
| chr6:170369158
|
A | G | 1 | a0002c0003t0002g0117 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2283+10840A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170369158 | ||||||
| chr6:170369406
|
G | C | 89 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(86): Show | 90 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.2283+11088G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170369406 | ||||||
| chr6:170369582
|
T | A | 153 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(150): Show | 157 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.2283+11264T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170369582 | ||||||
| chr6:170369617
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0250 | 2 | HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2283+11299G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170369617 | ||||||
| chr6:170369630
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2283+11312C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170369630 | ||||||
| chr6:170369639
|
G | A | 1 | a0001c0001t0010g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2283+11321G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170369639 | ||||||
| chr6:170369665
|
C | T | 8 | a0001c0002t0004g0022a0001c0002t0004g0023a0001c0002t0004g0025others(5): Show | 8 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2283+11347C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170369665 | ||||||
| chr6:170369689
|
G | GT | 52 | a0001c0001t0001g0241a0001c0001t0005g0171a0001c0001t0005g0208others(49): Show | 54 | HG00099.hp2 HG00558.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.2283+11390dupT | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170369689 | |||||
| chr6:170369690
|
T | G | 10 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(7): Show | 11 | HG01123.hp1 HG01243.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.2283+11372T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170369690 | ||||||
| chr6:170369898
|
G | A | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2283+11580G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170369898 | ||||||
| chr6:170369912
|
T | C | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2283+11594T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170369912 | ||||||
| chr6:170370026
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2283+11708A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170370026 | ||||||
| chr6:170370037
|
A | C | 1 | a0001c0002t0001g0071 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2283+11719A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170370037 | ||||||
| chr6:170370106
|
A | C | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2283+11788A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170370106 | ||||||
| chr6:170370153
|
G | C | 1 | a0004c0005t0009g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2283+11835G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170370153 | ||||||
| chr6:170370197
|
C | T | 2 | a0003c0004t0003g0159a0003c0004t0003g0160 | 2 | HG02056.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.2283+11879C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170370197 | ||||||
| chr6:170370202
|
C | T | 1 | a0001c0001t0010g0096 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2283+11884C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170370202 | ||||||
| chr6:170370267
|
T | C | 52 | a0001c0002t0001g0102a0001c0002t0004g0104a0001c0008t0001g0098others(49): Show | 53 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.2283+11949T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170370267 | ||||||
| chr6:170370375
|
C | T | 1 | a0007c0012t0001g0052 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2283+12057C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170370375 | ||||||
| chr6:170370508
|
A | C | 156 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(153): Show | 160 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.2283+12190A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170370508 | ||||||
| chr6:170370574
|
A | T | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276 | 3 | HG02572.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2283+12256A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170370574 | ||||||
| chr6:170370714
|
G | A | 1 | a0001c0001t0025g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2283+12396G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170370714 | ||||||
| chr6:170370942
|
T | C | 1 | a0004c0005t0009g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2283+12624T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170370942 | ||||||
| chr6:170370969
|
G | C | 1 | a0001c0002t0004g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2283+12651G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170370969 | ||||||
| chr6:170371037
|
A | G | 9 | a0003c0004t0003g0152a0003c0004t0003g0153a0003c0004t0003g0154others(6): Show | 9 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.2283+12719A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170371037 | ||||||
| chr6:170371240
|
G | A | 5 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(2): Show | 5 | HG00738.hp1 HG00741.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.2283+12922G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170371240 | ||||||
| chr6:170371477
|
G | A | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2283+13159G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170371477 | ||||||
| chr6:170371632
|
C | T | 4 | a0001c0008t0001g0098a0001c0008t0001g0099a0001c0009t0017g0093others(1): Show | 4 | HG02886.hp1 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2283+13314C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170371632 | ||||||
| chr6:170371714
|
C | A | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2283+13396C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170371714 | ||||||
| chr6:170371899
|
A | G | 2 | a0006c0010t0010g0019a0006c0010t0010g0020 | 2 | HG01099.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2283+13581A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170371899 | ||||||
| chr6:170371953
|
G | A | 1 | a0001c0001t0005g0214 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2283+13635G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170371953 | ||||||
| chr6:170372054
|
T | A | 1 | a0001c0002t0001g0063 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2283+13736T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170372054 | ||||||
| chr6:170372166
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0239a0001c0001t0001g0240others(1): Show | 5 | HG02280.hp2 HG02717.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2283+13848G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170372166 | ||||||
| chr6:170372369
|
C | T | 1 | a0001c0002t0001g0068 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2283+14051C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170372369 | ||||||
| chr6:170372419
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2283+14101C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170372419 | ||||||
| chr6:170372500
|
G | T | 1 | a0001c0001t0008g0195 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2283+14182G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170372500 | ||||||
| chr6:170372659
|
G | A | 131 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(128): Show | 134 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.2283+14341G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170372659 | ||||||
| chr6:170372677
|
C | G | 1 | a0001c0001t0005g0221 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2283+14359C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170372677 | ||||||
| chr6:170372803
|
A | G | 6 | a0001c0002t0004g0104a0001c0002t0029g0091a0001c0008t0001g0098others(3): Show | 6 | HG02055.hp2 HG02886.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2283+14485A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170372803 | ||||||
| chr6:170372811
|
A | ACTT | 3 | a0001c0002t0029g0091a0001c0008t0001g0098a0001c0008t0001g0099 | 3 | HG02886.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2283+14496_2283+14 others(9): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170372811 | |||||
| chr6:170372816
|
T | C | 1 | a0001c0009t0018g0092 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2283+14498T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170372816 | ||||||
| chr6:170372838
|
T | G | 1 | a0002c0003t0002g0137 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2283+14520T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170372838 | ||||||
| chr6:170372856
|
C | T | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2283+14538C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170372856 | ||||||
| chr6:170372949
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2283+14631C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170372949 | ||||||
| chr6:170372953
|
A | G | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2283+14635A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170372953 | ||||||
| chr6:170373236
|
T | G | 1 | a0009c0014t0009g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2283+14918T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170373236 | ||||||
| chr6:170373331
|
A | G | 3 | a0001c0002t0010g0103a0001c0002t0013g0039a0001c0002t0013g0040 | 3 | HG01891.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2284-14956A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170373331 | ||||||
| chr6:170373383
|
C | T | 5 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(2): Show | 6 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2284-14904C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170373383 | ||||||
| chr6:170373384
|
G | C | 1 | a0005c0007t0012g0002 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2284-14903G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170373384 | ||||||
| chr6:170373461
|
T | C | 2 | a0001c0002t0011g0016a0001c0002t0011g0017 | 2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2284-14826T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170373461 | ||||||
| chr6:170373536
|
T | C | 135 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(132): Show | 138 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.2284-14751T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170373536 | ||||||
| chr6:170373841
|
A | G | 2 | a0001c0002t0001g0073a0001c0002t0001g0074 | 2 | NA18942.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.2284-14446A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170373841 | ||||||
| chr6:170373901
|
A | G | 135 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(132): Show | 138 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.2284-14386A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170373901 | ||||||
| chr6:170373943
|
TGGTGCTG others(45): Show |
T | 1 | a0004c0005t0009g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2284-14299_2284-14 others(58): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170373943 | |||||
| chr6:170373959
|
C | T | 2 | a0001c0002t0001g0031a0001c0002t0024g0030 | 2 | HG01069.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2284-14328C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170373959 | ||||||
| chr6:170373972
|
C | G | 2 | a0001c0008t0001g0098a0001c0008t0001g0099 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2284-14315C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170373972 | ||||||
| chr6:170374014
|
G | C | 1 | a0001c0001t0010g0095 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2284-14273G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170374014 | ||||||
| chr6:170374153
|
G | C | 258 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.2284-14134G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170374153 | ||||||
| chr6:170374331
|
A | C | 259 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(256): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.2284-13956A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170374331 | ||||||
| chr6:170374353
|
T | A | 82 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(79): Show | 84 | HG00099.hp1 HG00558.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.2284-13934T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170374353 | ||||||
| chr6:170374436
|
A | G | 1 | a0001c0002t0001g0014 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2284-13851A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170374436 | ||||||
| chr6:170374529
|
A | G | 134 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(131): Show | 137 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.2284-13758A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170374529 | ||||||
| chr6:170374566
|
C | G | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2284-13721C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170374566 | ||||||
| chr6:170374572
|
C | T | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2284-13715C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170374572 | ||||||
| chr6:170374616
|
C | T | 1 | a0001c0002t0004g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2284-13671C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170374616 | ||||||
| chr6:170374673
|
G | A | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2284-13614G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170374673 | ||||||
| chr6:170374742
|
G | A | 1 | a0001c0001t0008g0197 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2284-13545G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170374742 | ||||||
| chr6:170374834
|
G | T | 1 | a0002c0003t0002g0141 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2284-13453G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170374834 | ||||||
| chr6:170374845
|
C | T | 39 | a0001c0002t0001g0001a0001c0002t0001g0046a0001c0002t0001g0047others(36): Show | 40 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(37): Show |
intron_variant | MODIFIER | c.2284-13442C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170374845 | ||||||
| chr6:170375377
|
A | G | 2 | a0001c0008t0001g0098a0001c0008t0001g0099 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2284-12910A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170375377 | ||||||
| chr6:170375531
|
T | C | 1 | a0001c0002t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2284-12756T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170375531 | ||||||
| chr6:170375651
|
A | G | 1 | a0001c0002t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2284-12636A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170375651 | ||||||
| chr6:170375775
|
G | A | 2 | a0001c0001t0005g0202a0001c0001t0005g0225 | 2 | HG00735.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2284-12512G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170375775 | ||||||
| chr6:170375801
|
C | T | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2284-12486C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170375801 | ||||||
| chr6:170375811
|
T | C | 2 | a0001c0002t0001g0071a0001c0017t0001g0080 | 2 | NA18747.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2284-12476T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170375811 | ||||||
| chr6:170375860
|
C | T | 5 | a0001c0002t0004g0104a0001c0008t0001g0098a0001c0008t0001g0099others(2): Show | 5 | HG02055.hp2 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2284-12427C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170375860 | ||||||
| chr6:170376006
|
G | A | 130 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(127): Show | 133 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.2284-12281G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376006 | ||||||
| chr6:170376126
|
A | G | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2284-12161A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376126 | ||||||
| chr6:170376275
|
T | G | 1 | a0004c0005t0009g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2284-12012T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376275 | ||||||
| chr6:170376449
|
A | G | 89 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(86): Show | 90 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.2284-11838A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376449 | ||||||
| chr6:170376584
|
C | T | 6 | a0004c0005t0001g0084a0004c0005t0001g0085a0004c0005t0001g0087others(3): Show | 6 | HG03041.hp2 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2284-11703C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376584 | ||||||
| chr6:170376605
|
G | C | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2284-11682G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376605 | ||||||
| chr6:170376609
|
C | G | 2 | a0001c0002t0001g0012a0001c0002t0001g0014 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2284-11678C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376609 | ||||||
| chr6:170376621
|
T | C | 1 | a0009c0014t0009g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2284-11666T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376621 | ||||||
| chr6:170376631
|
G | A | 33 | a0002c0003t0001g0134a0002c0003t0002g0106a0002c0003t0002g0107others(30): Show | 33 | HG00558.hp2 HG00673.hp2 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.2284-11656G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376631 | ||||||
| chr6:170376729
|
G | A | 7 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2284-11558G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376729 | ||||||
| chr6:170376735
|
C | T | 2 | a0001c0001t0006g0172a0001c0001t0006g0174 | 2 | HG01496.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2284-11552C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376735 | ||||||
| chr6:170376761
|
G | C | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2284-11526G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376761 | ||||||
| chr6:170376802
|
G | A | 5 | a0001c0002t0004g0104a0001c0008t0001g0098a0001c0008t0001g0099others(2): Show | 5 | HG02055.hp2 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2284-11485G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376802 | ||||||
| chr6:170376819
|
G | C | 35 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(32): Show | 35 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.2284-11468G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376819 | ||||||
| chr6:170376890
|
G | C | 78 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(75): Show | 80 | HG00099.hp1 HG00558.hp1 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.2284-11397G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376890 | ||||||
| chr6:170376948
|
G | A | 131 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(128): Show | 134 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.2284-11339G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376948 | ||||||
| chr6:170376952
|
G | A | 131 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(128): Show | 134 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.2284-11335G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376952 | ||||||
| chr6:170376953
|
A | G | 131 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(128): Show | 134 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.2284-11334A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376953 | ||||||
| chr6:170376957
|
C | G | 1 | a0001c0002t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2284-11330C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376957 | ||||||
| chr6:170376958
|
AG | A | 131 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(128): Show | 134 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.2284-11326delG | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170376958 | |||||
| chr6:170376960
|
G | C | 131 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(128): Show | 134 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.2284-11327G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376960 | ||||||
| chr6:170376968
|
T | TGTGCTGT others(359): Show |
1 | a0001c0001t0016g0199 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2284-11041_2284-11 others(372): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170376968 | |||||
| chr6:170376968
|
T | TGTGCTGT others(359): Show |
25 | a0001c0001t0001g0245a0001c0001t0001g0247a0001c0001t0001g0248others(22): Show | 25 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.2284-11155_2284-10 others(372): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170376968 | |||||
| chr6:170376968
|
T | TGTGCTGT others(359): Show |
1 | a0001c0001t0001g0204 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2284-10971_2284-10 others(372): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170376968 | |||||
| chr6:170376969
|
G | C | 2 | a0001c0008t0001g0098a0001c0008t0001g0099 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2284-11318G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376969 | ||||||
| chr6:170376981
|
C | CGCGTCCC others(54): Show |
1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2284-11246_2284-11 others(67): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170376981 | |||||
| chr6:170376984
|
G | A | 1 | a0001c0002t0013g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2284-11303G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376984 | ||||||
| chr6:170376999
|
C | T | 22 | a0001c0002t0001g0105a0003c0004t0003g0005a0003c0004t0003g0152others(19): Show | 23 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.2284-11288C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170376999 | ||||||
| chr6:170377003
|
T | C | 50 | a0001c0002t0001g0037a0001c0002t0001g0038a0001c0002t0001g0066others(47): Show | 51 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.2284-11284T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377003 | ||||||
| chr6:170377003
|
T | TGGGAGAA others(2067): Show |
1 | a0001c0002t0001g0062 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2284-11224_2284-11 others(2080): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377003 | |||||
| chr6:170377003
|
T | TGGGAGAA others(54): Show |
1 | a0001c0002t0001g0100 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2284-11235_2284-11 others(67): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377003 | |||||
| chr6:170377012
|
A | ACAGGCTC others(54): Show |
20 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(17): Show | 21 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2284-11228_2284-11 others(67): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377012 | |||||
| chr6:170377021
|
C | CGCTGCTC others(54): Show |
1 | a0001c0002t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2284-11224_2284-11 others(67): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377021 | |||||
| chr6:170377042
|
C | T | 4 | a0001c0008t0001g0098a0001c0008t0001g0099a0001c0009t0017g0093others(1): Show | 4 | HG02886.hp1 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2284-11245C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377042 | ||||||
| chr6:170377053
|
A | ACCCAGAC others(115): Show |
1 | a0001c0002t0001g0059 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2284-11224_2284-11 others(128): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377053 | |||||
| chr6:170377053
|
A | ACCCAGAC others(1945): Show |
3 | a0001c0002t0001g0054a0001c0002t0001g0060a0001c0002t0001g0066 | 3 | HG02523.hp1 HG03927.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.2284-11224_2284-11 others(1958): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377053 | |||||
| chr6:170377053
|
A | ACCCAGAC others(1945): Show |
1 | a0001c0002t0001g0064 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2284-11224_2284-11 others(1958): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377053 | |||||
| chr6:170377053
|
A | ACCCAGAC others(1945): Show |
1 | a0001c0002t0001g0070 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2284-11224_2284-11 others(1958): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377053 | |||||
| chr6:170377053
|
A | ACCCAGAC others(603): Show |
22 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(19): Show | 23 | HG00099.hp2 HG00673.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.2284-11224_2284-11 others(616): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377053 | |||||
| chr6:170377060
|
C | T | 2 | a0001c0002t0001g0105a0003c0004t0003g0161 | 2 | HG00639.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.2284-11227C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377060 | ||||||
| chr6:170377064
|
T | C | 92 | a0001c0002t0001g0001a0001c0002t0001g0031a0001c0002t0001g0036others(89): Show | 94 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.2284-11223T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377064 | ||||||
| chr6:170377064
|
T | TGGGAGAA others(1579): Show |
2 | a0006c0010t0010g0019a0006c0010t0010g0020 | 2 | HG01099.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2284-11174_2284-11 others(1592): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377064 | |||||
| chr6:170377075
|
A | AGGCTCAC others(542): Show |
1 | a0002c0003t0002g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2284-11174_2284-11 others(555): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377075 | |||||
| chr6:170377075
|
A | G | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2284-11212A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377075 | ||||||
| chr6:170377076
|
G | A | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2284-11211G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377076 | ||||||
| chr6:170377082
|
C | CGCTGCTC others(115): Show |
26 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(23): Show | 26 | HG00099.hp1 HG00558.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.2284-11174_2284-11 others(128): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377082 | |||||
| chr6:170377114
|
T | A | 81 | a0001c0001t0014g0226a0001c0002t0001g0001a0001c0002t0001g0021others(78): Show | 83 | HG00558.hp1 HG00642.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.2284-11173T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377114 | ||||||
| chr6:170377121
|
T | C | 135 | a0001c0001t0014g0226a0001c0002t0001g0001a0001c0002t0001g0012others(132): Show | 138 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.2284-11166T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377121 | ||||||
| chr6:170377125
|
T | C | 126 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(123): Show | 128 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.2284-11162T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377125 | ||||||
| chr6:170377134
|
A | G | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2284-11153A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377134 | ||||||
| chr6:170377136
|
A | G | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2284-11151A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377136 | ||||||
| chr6:170377137
|
G | A | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2284-11150G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377137 | ||||||
| chr6:170377143
|
C | CGCTGCTC others(359): Show |
1 | a0001c0001t0019g0211 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2284-10790_2284-10 others(372): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377143 | |||||
| chr6:170377143
|
C | CGCTGCTC others(359): Show |
1 | a0001c0002t0001g0067 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2284-11113_2284-11 others(372): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377143 | |||||
| chr6:170377152
|
G | GTGCTGTG others(481): Show |
2 | a0001c0009t0017g0093a0001c0009t0018g0092 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2284-11113_2284-11 others(494): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377152 | |||||
| chr6:170377175
|
A | ACCCAGAC others(54): Show |
1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2284-11106_2284-11 others(67): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377175 | |||||
| chr6:170377175
|
A | T | 72 | a0001c0002t0001g0001a0001c0002t0001g0021a0001c0002t0001g0036others(69): Show | 73 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.2284-11112A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377175 | ||||||
| chr6:170377182
|
T | C | 136 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(133): Show | 139 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.2284-11105T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377182 | ||||||
| chr6:170377186
|
T | C | 132 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(129): Show | 135 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.2284-11101T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377186 | ||||||
| chr6:170377188
|
G | A | 1 | a0001c0002t0001g0059 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2284-11099G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377188 | ||||||
| chr6:170377197
|
G | A | 137 | a0001c0001t0001g0272a0001c0002t0001g0001a0001c0002t0001g0012others(134): Show | 140 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.2284-11090G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377197 | ||||||
| chr6:170377198
|
A | G | 136 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(133): Show | 139 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.2284-11089A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377198 | ||||||
| chr6:170377204
|
C | G | 31 | a0001c0002t0001g0021a0001c0002t0004g0022a0001c0002t0004g0029others(28): Show | 31 | HG00642.hp1 HG01081.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2284-11083C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377204 | ||||||
| chr6:170377236
|
T | A | 11 | a0001c0002t0001g0054a0001c0002t0001g0060a0001c0002t0001g0062others(8): Show | 11 | HG00639.hp1 HG02273.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.2284-11051T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377236 | ||||||
| chr6:170377236
|
T | TCCCAGAC others(115): Show |
1 | a0001c0002t0001g0071 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2284-11045_2284-11 others(128): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377236 | |||||
| chr6:170377236
|
T | TCCCAGAC others(237): Show |
5 | a0001c0002t0001g0056a0001c0002t0001g0065a0001c0002t0004g0069others(2): Show | 5 | HG00558.hp1 HG02129.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.2284-11045_2284-11 others(250): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377236 | |||||
| chr6:170377243
|
T | C | 133 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(130): Show | 136 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.2284-11044T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377243 | ||||||
| chr6:170377247
|
T | C | 134 | a0001c0001t0016g0198a0001c0001t0016g0199a0001c0002t0001g0001others(131): Show | 137 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.2284-11040T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377247 | ||||||
| chr6:170377249
|
G | A | 1 | a0001c0002t0001g0100 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2284-11038G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377249 | ||||||
| chr6:170377249
|
G | GGAGAACA others(54): Show |
1 | a0001c0002t0001g0081 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2284-11032_2284-11 others(67): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377249 | |||||
| chr6:170377256
|
G | A | 152 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(149): Show | 156 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.2284-11031G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377256 | ||||||
| chr6:170377258
|
A | G | 20 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(17): Show | 21 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2284-11029A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377258 | ||||||
| chr6:170377259
|
G | A | 20 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(17): Show | 21 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2284-11028G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377259 | ||||||
| chr6:170377265
|
C | CGCTGCTC others(115): Show |
1 | a0001c0002t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2284-10984_2284-10 others(128): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377265 | |||||
| chr6:170377265
|
C | G | 5 | a0001c0008t0001g0098a0001c0008t0001g0099a0005c0007t0012g0002others(2): Show | 6 | HG02055.hp1 HG02451.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2284-11022C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377265 | ||||||
| chr6:170377289
|
G | T | 3 | a0001c0002t0010g0103a0001c0002t0013g0039a0001c0002t0013g0040 | 3 | HG01891.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2284-10998G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377289 | ||||||
| chr6:170377297
|
T | A | 37 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(34): Show | 37 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.2284-10990T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377297 | ||||||
| chr6:170377297
|
T | TCCCAGAC others(2006): Show |
1 | a0001c0002t0001g0068 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2284-10984_2284-10 others(2019): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377297 | |||||
| chr6:170377304
|
T | C | 136 | a0001c0001t0016g0198a0001c0001t0016g0199a0001c0002t0001g0001others(133): Show | 139 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.2284-10983T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377304 | ||||||
| chr6:170377304
|
T | TGCCTGGG others(237): Show |
19 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(16): Show | 20 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.2284-10980_2284-10 others(250): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377304 | |||||
| chr6:170377304
|
T | TGCCTGGG others(359): Show |
1 | a0003c0004t0003g0161 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2284-10980_2284-10 others(372): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377304 | |||||
| chr6:170377308
|
C | T | 26 | a0001c0002t0001g0105a0001c0002t0013g0039a0001c0002t0013g0040others(23): Show | 27 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.2284-10979C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377308 | ||||||
| chr6:170377310
|
G | A | 22 | a0001c0002t0001g0001a0001c0002t0001g0046a0001c0002t0001g0047others(19): Show | 23 | HG00673.hp1 HG01981.hp1 HG02293.hp2 others(20): Show |
intron_variant | MODIFIER | c.2284-10977G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377310 | ||||||
| chr6:170377310
|
G | AGAGAACA others(115): Show |
1 | a0001c0002t0001g0076 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2284-10978_2284-10 others(128): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377310 | ||||||
| chr6:170377317
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2284-10970A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377317 | ||||||
| chr6:170377319
|
A | G | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2284-10968A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377319 | ||||||
| chr6:170377320
|
G | A | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2284-10967G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377320 | ||||||
| chr6:170377335
|
G | GTGCTGTG others(10912): Show |
1 | a0001c0002t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2284-10919_2284-10 others(10925): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377335 | |||||
| chr6:170377348
|
G | A | 2 | a0001c0008t0001g0098a0001c0008t0001g0099 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2284-10939G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377348 | ||||||
| chr6:170377358
|
A | ACCCAGAC others(54): Show |
1 | a0001c0002t0001g0094 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2284-10919_2284-10 others(67): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377358 | |||||
| chr6:170377358
|
A | T | 17 | a0001c0002t0001g0021a0001c0002t0001g0067a0001c0002t0001g0081others(14): Show | 17 | HG00639.hp1 HG00642.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.2284-10929A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377358 | ||||||
| chr6:170377365
|
C | T | 1 | a0003c0004t0003g0162 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2284-10922C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377365 | ||||||
| chr6:170377369
|
T | C | 129 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(126): Show | 132 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.2284-10918T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377369 | ||||||
| chr6:170377369
|
T | G | 1 | a0011c0011t0001g0129 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2284-10918T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377369 | ||||||
| chr6:170377372
|
G | C | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2284-10915G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377372 | ||||||
| chr6:170377376
|
A | G | 1 | a0001c0002t0001g0067 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2284-10911A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377376 | ||||||
| chr6:170377379
|
C | T | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2284-10908C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377379 | ||||||
| chr6:170377380
|
A | C | 1 | a0001c0002t0001g0067 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2284-10907A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377380 | ||||||
| chr6:170377395
|
G | T | 2 | a0001c0008t0001g0098a0001c0008t0001g0099 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2284-10892G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377395 | ||||||
| chr6:170377401
|
G | GTGCACAC others(847): Show |
1 | a0001c0002t0001g0075 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2284-10869_2284-10 others(860): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377401 | |||||
| chr6:170377401
|
G | GTGCACAC others(786): Show |
18 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(15): Show | 19 | HG02293.hp2 HG02615.hp2 HG02976.hp1 others(16): Show |
intron_variant | MODIFIER | c.2284-10869_2284-10 others(799): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377401 | |||||
| chr6:170377401
|
G | GTGCACAC others(969): Show |
3 | a0001c0002t0001g0051a0001c0002t0001g0061a0001c0002t0001g0078 | 3 | HG01981.hp1 NA18955.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.2284-10869_2284-10 others(982): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377401 | |||||
| chr6:170377403
|
G | GCACACGC others(1335): Show |
1 | a0001c0002t0001g0049 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2284-10869_2284-10 others(1348): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377403 | |||||
| chr6:170377403
|
G | T | 6 | a0001c0002t0001g0054a0001c0002t0001g0060a0001c0002t0001g0062others(3): Show | 6 | HG02273.hp1 HG02523.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.2284-10884G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377403 | ||||||
| chr6:170377419
|
A | ACCCAGAC others(5117): Show |
2 | a0005c0007t0012g0003a0005c0007t0028g0003 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2284-10858_2284-10 others(5130): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377419 | |||||
| chr6:170377419
|
A | ACCCAGAC others(5117): Show |
1 | a0005c0007t0012g0002 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2284-10858_2284-10 others(5130): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377419 | |||||
| chr6:170377419
|
A | T | 5 | a0001c0002t0001g0050a0001c0002t0001g0059a0001c0002t0001g0071others(2): Show | 5 | HG00639.hp1 HG02056.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.2284-10868A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377419 | ||||||
| chr6:170377426
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2284-10861C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377426 | ||||||
| chr6:170377430
|
T | C | 130 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(127): Show | 133 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.2284-10857T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377430 | ||||||
| chr6:170377430
|
T | TGGGAGAA others(603): Show |
1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2284-10817_2284-10 others(616): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377430 | |||||
| chr6:170377437
|
ACACAGGC others(54): Show |
A | 1 | a0001c0001t0010g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2284-10807_2284-10 others(67): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377437 | |||||
| chr6:170377438
|
C | CACGAGCT others(359): Show |
1 | a0003c0004t0003g0162 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2284-10847_2284-10 others(372): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377438 | |||||
| chr6:170377441
|
A | G | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2284-10846A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377441 | ||||||
| chr6:170377442
|
G | A | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2284-10845G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377442 | ||||||
| chr6:170377466
|
A | G | 20 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(17): Show | 21 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2284-10821A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377466 | ||||||
| chr6:170377470
|
G | A | 20 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(17): Show | 21 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2284-10817G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377470 | ||||||
| chr6:170377471
|
C | A | 1 | a0002c0003t0002g0123 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2284-10816C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377471 | ||||||
| chr6:170377478
|
A | G | 20 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(17): Show | 21 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2284-10809A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377478 | ||||||
| chr6:170377480
|
T | A | 15 | a0001c0002t0001g0021a0001c0002t0001g0050a0001c0002t0001g0059others(12): Show | 15 | HG00642.hp1 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.2284-10807T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377480 | ||||||
| chr6:170377480
|
T | TCCCAGAC others(54): Show |
9 | a0002c0003t0002g0110a0002c0003t0002g0115a0002c0003t0002g0126others(6): Show | 9 | HG00673.hp2 HG01255.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.2284-10801_2284-10 others(67): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377480 | |||||
| chr6:170377480
|
T | TCCCAGAC others(664): Show |
3 | a0002c0003t0002g0117a0002c0003t0002g0122a0002c0003t0002g0124 | 3 | NA18612.hp2 NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2284-10801_2284-10 others(677): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377480 | |||||
| chr6:170377480
|
T | TCCCAGAC others(54): Show |
1 | a0001c0009t0018g0092 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2284-10801_2284-10 others(67): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377480 | |||||
| chr6:170377487
|
T | C | 140 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(137): Show | 144 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.2284-10800T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377487 | ||||||
| chr6:170377491
|
T | C | 131 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(128): Show | 134 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.2284-10796T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377491 | ||||||
| chr6:170377491
|
T | TGGGAGAA others(54): Show |
1 | a0001c0009t0017g0093 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2284-10790_2284-10 others(67): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377491 | |||||
| chr6:170377494
|
G | A | 1 | a0004c0005t0009g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2284-10793G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377494 | ||||||
| chr6:170377498
|
G | A | 131 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(128): Show | 134 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.2284-10789G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377498 | ||||||
| chr6:170377498
|
G | GCACCGGC others(54): Show |
1 | a0002c0003t0002g0123 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2284-10786_2284-10 others(67): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377498 | |||||
| chr6:170377500
|
A | G | 3 | a0001c0002t0010g0103a0001c0002t0013g0039a0001c0002t0013g0040 | 3 | HG01891.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2284-10787A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377500 | ||||||
| chr6:170377502
|
A | C | 1 | a0001c0002t0001g0067 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2284-10785A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377502 | ||||||
| chr6:170377523
|
G | A | 1 | a0001c0002t0001g0067 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2284-10764G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377523 | ||||||
| chr6:170377541
|
A | ACCCAGAC others(115): Show |
1 | a0002c0003t0002g0118 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2284-10736_2284-10 others(128): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377541 | |||||
| chr6:170377541
|
A | ACCCAGAC others(1884): Show |
1 | a0001c0002t0001g0094 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2284-10736_2284-10 others(1897): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377541 | |||||
| chr6:170377541
|
A | ACCCAGAC others(1885): Show |
1 | a0001c0002t0001g0081 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2284-10736_2284-10 others(1898): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377541 | |||||
| chr6:170377541
|
A | ACCCAGAC others(1701): Show |
4 | a0001c0002t0001g0056a0001c0002t0004g0069a0001c0017t0001g0080others(1): Show | 4 | HG00558.hp1 HG03492.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.2284-10736_2284-10 others(1714): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377541 | |||||
| chr6:170377541
|
A | T | 32 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(29): Show | 33 | HG00673.hp1 HG01981.hp1 HG02015.hp2 others(30): Show |
intron_variant | MODIFIER | c.2284-10746A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377541 | ||||||
| chr6:170377552
|
T | C | 132 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(129): Show | 135 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.2284-10735T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377552 | ||||||
| chr6:170377570
|
C | G | 1 | a0001c0002t0001g0065 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2284-10717C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377570 | ||||||
| chr6:170377602
|
T | A | 52 | a0001c0002t0001g0049a0001c0002t0001g0050a0001c0002t0001g0054others(49): Show | 54 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.2284-10685T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377602 | ||||||
| chr6:170377609
|
T | C | 143 | a0001c0001t0010g0083a0001c0002t0001g0001a0001c0002t0001g0012others(140): Show | 146 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.2284-10678T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377609 | ||||||
| chr6:170377613
|
T | C | 129 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(126): Show | 132 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.2284-10674T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377613 | ||||||
| chr6:170377620
|
G | A | 122 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(119): Show | 125 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.2284-10667G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377620 | ||||||
| chr6:170377620
|
G | GCACCGGC others(664): Show |
1 | a0002c0003t0021g0113 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2284-10664_2284-10 others(677): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377620 | |||||
| chr6:170377620
|
G | GCACCGGC others(7008): Show |
1 | a0002c0003t0002g0120 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2284-10664_2284-10 others(7021): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377620 | |||||
| chr6:170377620
|
G | GCACCGGC others(6215): Show |
1 | a0002c0003t0002g0150 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2284-10664_2284-10 others(6228): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377620 | |||||
| chr6:170377624
|
A | C | 3 | a0002c0003t0002g0107a0002c0003t0002g0127a0011c0011t0001g0129 | 3 | HG03942.hp1 NA18969.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.2284-10663A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377624 | ||||||
| chr6:170377624
|
A | CGGCTCAC others(115): Show |
4 | a0002c0003t0002g0121a0002c0003t0002g0133a0002c0003t0007g0112others(1): Show | 4 | HG02155.hp1 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2284-10664_2284-10 others(128): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377624 | ||||||
| chr6:170377624
|
A | CGGCTCAC others(176): Show |
1 | a0002c0003t0002g0137 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2284-10664_2284-10 others(189): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377624 | ||||||
| chr6:170377624
|
A | CGGCTCAC others(6215): Show |
2 | a0002c0003t0002g0111a0002c0003t0002g0149 | 2 | NA19065.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.2284-10664_2284-10 others(6228): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377624 | ||||||
| chr6:170377639
|
G | T | 2 | a0001c0008t0001g0098a0001c0008t0001g0099 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2284-10648G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377639 | ||||||
| chr6:170377640
|
G | C | 2 | a0001c0008t0001g0098a0001c0008t0001g0099 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2284-10647G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377640 | ||||||
| chr6:170377647
|
G | GCACACGC others(1884): Show |
1 | a0001c0002t0001g0100 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2284-10625_2284-10 others(1897): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377647 | |||||
| chr6:170377663
|
A | ACCCAGAC others(54): Show |
5 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(2): Show | 6 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2284-10587_2284-10 others(67): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377663 | |||||
| chr6:170377663
|
A | T | 39 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(36): Show | 40 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.2284-10624A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377663 | ||||||
| chr6:170377665
|
C | G | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2284-10622C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377665 | ||||||
| chr6:170377674
|
T | C | 128 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(125): Show | 131 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.2284-10613T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377674 | ||||||
| chr6:170377681
|
A | G | 1 | a0001c0001t0010g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2284-10606A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377681 | ||||||
| chr6:170377685
|
A | AGGCTCAC others(54): Show |
2 | a0001c0002t0001g0105a0002c0003t0002g0141 | 2 | HG00639.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.2284-10553_2284-10 others(67): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377685 | |||||
| chr6:170377685
|
A | G | 1 | a0003c0004t0003g0162 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2284-10602A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377685 | ||||||
| chr6:170377686
|
G | A | 1 | a0003c0004t0003g0162 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2284-10601G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377686 | ||||||
| chr6:170377686
|
G | GGCTCACG others(115): Show |
20 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(17): Show | 21 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2284-10564_2284-10 others(128): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377686 | |||||
| chr6:170377692
|
C | G | 2 | a0001c0002t0001g0059a0001c0002t0001g0071 | 2 | HG03834.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2284-10595C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377692 | ||||||
| chr6:170377695
|
T | G | 2 | a0001c0009t0017g0093a0001c0009t0018g0092 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2284-10592T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377695 | ||||||
| chr6:170377724
|
T | A | 42 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(39): Show | 43 | HG00099.hp1 HG00099.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.2284-10563T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377724 | ||||||
| chr6:170377724
|
T | TCCCAGAC others(1457): Show |
1 | a0001c0008t0001g0098 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2284-10553_2284-10 others(1470): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377724 | |||||
| chr6:170377724
|
T | TCCCAGAC others(1396): Show |
1 | a0001c0008t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2284-10553_2284-10 others(1409): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377724 | |||||
| chr6:170377725
|
C | CCCAGACG others(53): Show |
1 | a0011c0011t0001g0129 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2284-10553_2284-10 others(66): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377725 | |||||
| chr6:170377735
|
T | C | 129 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(126): Show | 132 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.2284-10552T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377735 | ||||||
| chr6:170377742
|
A | G | 4 | a0002c0003t0002g0109a0002c0003t0002g0142a0002c0003t0002g0143others(1): Show | 4 | HG01123.hp2 HG01943.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2284-10545A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377742 | ||||||
| chr6:170377746
|
A | C | 4 | a0002c0003t0002g0109a0002c0003t0002g0142a0002c0003t0002g0143others(1): Show | 4 | HG01123.hp2 HG01943.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2284-10541A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377746 | ||||||
| chr6:170377761
|
T | G | 133 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(130): Show | 136 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.2284-10526T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377761 | ||||||
| chr6:170377762
|
G | C | 1 | a0001c0002t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2284-10525G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377762 | ||||||
| chr6:170377777
|
G | A | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2284-10510G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377777 | ||||||
| chr6:170377785
|
T | A | 30 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(27): Show | 31 | HG00673.hp1 HG01099.hp1 HG01981.hp1 others(28): Show |
intron_variant | MODIFIER | c.2284-10502T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377785 | ||||||
| chr6:170377792
|
T | C | 134 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(131): Show | 137 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.2284-10495T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377792 | ||||||
| chr6:170377796
|
T | C | 126 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(123): Show | 129 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.2284-10491T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377796 | ||||||
| chr6:170377803
|
A | G | 1 | a0001c0002t0001g0065 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2284-10484A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377803 | ||||||
| chr6:170377807
|
A | C | 2 | a0001c0002t0001g0065a0005c0007t0012g0002 | 3 | HG02055.hp1 HG02129.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2284-10480A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377807 | ||||||
| chr6:170377814
|
C | G | 1 | a0001c0002t0001g0050 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2284-10473C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377814 | ||||||
| chr6:170377822
|
G | T | 6 | a0001c0008t0001g0098a0001c0008t0001g0099a0002c0003t0002g0111others(3): Show | 6 | HG02886.hp1 NA18955.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.2284-10465G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377822 | ||||||
| chr6:170377823
|
G | C | 6 | a0001c0008t0001g0098a0001c0008t0001g0099a0002c0003t0002g0111others(3): Show | 6 | HG02886.hp1 NA18955.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.2284-10464G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377823 | ||||||
| chr6:170377827
|
T | C | 1 | a0002c0003t0021g0113 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2284-10460T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377827 | ||||||
| chr6:170377832
|
A | ACACGCGT others(298): Show |
1 | a0001c0002t0001g0076 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2284-10442_2284-10 others(311): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377832 | |||||
| chr6:170377846
|
T | A | 50 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(47): Show | 50 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.2284-10441T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377846 | ||||||
| chr6:170377853
|
T | C | 134 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(131): Show | 137 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.2284-10434T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377853 | ||||||
| chr6:170377857
|
T | C | 132 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(129): Show | 135 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.2284-10430T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377857 | ||||||
| chr6:170377864
|
G | A | 78 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(75): Show | 79 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.2284-10423G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377864 | ||||||
| chr6:170377868
|
C | A | 78 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(75): Show | 79 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.2284-10419C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377868 | ||||||
| chr6:170377868
|
C | CGGCTCAC others(5056): Show |
1 | a0002c0003t0002g0115 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2284-10400_2284-10 others(5069): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377868 | |||||
| chr6:170377868
|
C | CGGCTCAC others(6401): Show |
1 | a0002c0003t0021g0113 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2284-10400_2284-10 others(6414): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377868 | |||||
| chr6:170377882
|
C | G | 1 | a0001c0001t0001g0264 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2284-10405C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377882 | ||||||
| chr6:170377888
|
T | C | 1 | a0002c0003t0002g0141 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2284-10399T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377888 | ||||||
| chr6:170377907
|
A | T | 49 | a0001c0002t0001g0021a0001c0002t0001g0050a0001c0002t0001g0071others(46): Show | 50 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.2284-10380A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377907 | ||||||
| chr6:170377914
|
C | CGCCCGGG others(4812): Show |
1 | a0002c0003t0002g0142 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(4825): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(5605): Show |
1 | a0002c0003t0002g0141 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(5618): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(6398): Show |
1 | a0002c0003t0023g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(6411): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(6398): Show |
1 | a0002c0003t0002g0135 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(6411): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(6520): Show |
1 | a0002c0003t0002g0126 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(6533): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(7069): Show |
1 | a0002c0003t0001g0134 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(7082): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(6032): Show |
1 | a0002c0003t0002g0143 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(6045): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(5605): Show |
1 | a0002c0003t0022g0144 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(5618): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(5605): Show |
1 | a0002c0003t0002g0109 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(5618): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(7069): Show |
1 | a0002c0003t0007g0112 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(7082): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(7070): Show |
1 | a0002c0003t0007g0145 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(7083): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(6398): Show |
1 | a0002c0003t0002g0127 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(6411): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(1396): Show |
2 | a0006c0010t0010g0019a0006c0010t0010g0020 | 2 | HG01099.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2284-10370_2284-10 others(1409): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2982): Show |
1 | a0001c0002t0004g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(2995): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2982): Show |
3 | a0001c0002t0004g0022a0001c0002t0004g0178a0001c0002t0004g0179 | 3 | HG01099.hp2 HG01175.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.2284-10370_2284-10 others(2995): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2921): Show |
1 | a0001c0002t0004g0029 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(2934): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(3043): Show |
1 | a0001c0002t0004g0180 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(3056): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2677): Show |
1 | a0001c0002t0004g0034 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(2690): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2921): Show |
1 | a0004c0005t0009g0090 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(2934): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(3104): Show |
1 | a0001c0002t0001g0021 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(3117): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(9135): Show |
1 | a0011c0011t0001g0129 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(9148): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2189): Show |
1 | a0001c0002t0001g0059 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(2202): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(298): Show |
1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(311): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(298): Show |
1 | a0001c0002t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(311): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(6459): Show |
1 | a0002c0003t0002g0124 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(6472): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(5727): Show |
1 | a0002c0003t0002g0136 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(5740): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(6398): Show |
1 | a0002c0003t0002g0148 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(6411): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(6460): Show |
1 | a0002c0003t0002g0117 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(6473): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(6459): Show |
1 | a0002c0003t0002g0123 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(6472): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(8167): Show |
1 | a0002c0003t0002g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(8180): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(6276): Show |
1 | a0002c0003t0002g0146 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(6289): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(9839): Show |
1 | a0002c0003t0002g0131 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(9852): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(9265): Show |
1 | a0002c0003t0002g0133 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(9278): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(6947): Show |
1 | a0002c0003t0002g0121 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(6960): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(6947): Show |
1 | a0002c0003t0002g0137 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(6960): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(6581): Show |
1 | a0002c0003t0002g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(6594): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(8045): Show |
1 | a0002c0003t0002g0118 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(8058): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(9083): Show |
1 | a0002c0003t0002g0107 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(9096): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(1518): Show |
2 | a0001c0002t0001g0077a0001c0002t0001g0079 | 2 | HG02293.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.2284-10370_2284-10 others(1531): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2799): Show |
1 | a0001c0002t0004g0026 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(2812): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2799): Show |
1 | a0001c0002t0004g0028 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(2812): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2860): Show |
3 | a0001c0002t0004g0023a0001c0002t0004g0025a0001c0002t0004g0033 | 3 | HG00099.hp1 HG01106.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2284-10370_2284-10 others(2873): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2921): Show |
1 | a0001c0002t0004g0027 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(2934): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(3348): Show |
1 | a0001c0002t0001g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(3361): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2860): Show |
1 | a0001c0002t0001g0035 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(2873): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2921): Show |
1 | a0001c0002t0029g0091 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(2934): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2921): Show |
3 | a0001c0002t0001g0044a0001c0002t0001g0045a0001c0002t0001g0101 | 3 | HG02145.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2284-10370_2284-10 others(2934): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2921): Show |
3 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0001g0043 | 3 | HG02965.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2284-10370_2284-10 others(2934): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2982): Show |
2 | a0001c0002t0001g0031a0001c0002t0024g0030 | 2 | HG01069.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2284-10370_2284-10 others(2995): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2555): Show |
1 | a0001c0002t0001g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(2568): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(847): Show |
1 | a0001c0002t0001g0050 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(860): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2982): Show |
1 | a0001c0002t0001g0015 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(2995): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2982): Show |
6 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.2284-10370_2284-10 others(2995): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(1640): Show |
1 | a0001c0002t0001g0067 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(1653): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(1579): Show |
1 | a0001c0002t0001g0036 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(1592): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(1518): Show |
14 | a0001c0002t0001g0001a0001c0002t0001g0046a0001c0002t0001g0047others(11): Show | 15 | HG00673.hp1 HG01981.hp1 NA18612.hp1 others(12): Show |
intron_variant | MODIFIER | c.2284-10370_2284-10 others(1531): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2128): Show |
1 | a0001c0002t0001g0057 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(2141): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(1701): Show |
1 | a0001c0002t0001g0058 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(1714): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2616): Show |
1 | a0001c0002t0001g0097 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(2629): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(1579): Show |
1 | a0001c0002t0001g0037 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(1592): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(1579): Show |
1 | a0001c0002t0001g0038 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(1592): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(5117): Show |
1 | a0002c0003t0002g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(5130): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(5112): Show |
1 | a0002c0003t0002g0119 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(5125): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(5788): Show |
1 | a0002c0003t0002g0147 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(5801): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(359): Show |
13 | a0001c0002t0001g0049a0001c0002t0001g0054a0001c0002t0001g0056others(10): Show | 13 | HG00558.hp1 HG02015.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.2284-10370_2284-10 others(372): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(298): Show |
1 | a0001c0002t0001g0064 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(311): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(176): Show |
1 | a0001c0002t0004g0069 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(189): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2189): Show |
1 | a0001c0002t0001g0071 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(2202): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(2067): Show |
1 | a0001c0002t0001g0065 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(2080): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(237): Show |
1 | a0005c0007t0012g0002 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2284-10370_2284-10 others(250): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(237): Show |
2 | a0005c0007t0012g0003a0005c0007t0028g0003 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2284-10370_2284-10 others(250): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(5788): Show |
1 | a0002c0003t0002g0139 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(5801): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(6459): Show |
1 | a0002c0003t0002g0108 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(6472): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(6276): Show |
1 | a0002c0003t0002g0125 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(6289): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(5361): Show |
1 | a0002c0003t0002g0116 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(5374): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(6337): Show |
1 | a0002c0003t0002g0114 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(6350): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(5788): Show |
1 | a0002c0003t0002g0130 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(5801): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(5483): Show |
1 | a0002c0003t0002g0140 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2284-10370_2284-10 others(5496): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(5788): Show |
1 | a0002c0003t0002g0004 | 2 | HG00099.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2284-10370_2284-10 others(5801): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCCGGG others(5788): Show |
2 | a0002c0003t0002g0128a0002c0003t0002g0132 | 2 | HG01256.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.2284-10370_2284-10 others(5801): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCTGGG others(847): Show |
1 | a0001c0009t0017g0093 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2284-10363_2284-10 others(860): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | CGCCTGGG others(847): Show |
1 | a0001c0009t0018g0092 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2284-10363_2284-10 others(860): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170377914 | |||||
| chr6:170377914
|
C | T | 9 | a0001c0002t0001g0076a0001c0008t0001g0098a0001c0008t0001g0099others(6): Show | 9 | HG02056.hp2 HG02886.hp1 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.2284-10373C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377914 | ||||||
| chr6:170377931
|
T | C | 1 | a0001c0002t0004g0022 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2284-10356T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170377931 | ||||||
| chr6:170378116
|
C | T | 1 | a0001c0006t0001g0255 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2284-10171C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170378116 | ||||||
| chr6:170378246
|
C | A | 1 | a0001c0001t0025g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2284-10041C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170378246 | ||||||
| chr6:170378277
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2284-10010A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170378277 | ||||||
| chr6:170378387
|
G | A | 27 | a0001c0001t0001g0204a0001c0001t0001g0245a0001c0001t0001g0247others(24): Show | 27 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.2284-9900G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170378387 | ||||||
| chr6:170378387
|
G | T | 1 | a0002c0003t0021g0113 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2284-9900G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170378387 | ||||||
| chr6:170378472
|
C | A | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2284-9815C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170378472 | ||||||
| chr6:170378477
|
C | G | 3 | a0001c0002t0004g0104a0001c0008t0001g0098a0001c0008t0001g0099 | 3 | HG02055.hp2 HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2284-9810C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170378477 | ||||||
| chr6:170378488
|
G | A | 2 | a0001c0001t0001g0204a0002c0003t0002g0109 | 2 | HG01943.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2284-9799G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170378488 | ||||||
| chr6:170378583
|
G | A | 134 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(131): Show | 137 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.2284-9704G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170378583 | ||||||
| chr6:170378598
|
A | G | 133 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(130): Show | 136 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.2284-9689A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170378598 | ||||||
| chr6:170378598
|
A | T | 1 | a0001c0002t0004g0034 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2284-9689A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170378598 | ||||||
| chr6:170378599
|
G | T | 2 | a0005c0007t0012g0003a0005c0007t0028g0003 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2284-9688G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170378599 | ||||||
| chr6:170378798
|
G | T | 1 | a0002c0003t0002g0116 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2284-9489G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170378798 | ||||||
| chr6:170378949
|
C | T | 36 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(33): Show | 36 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.2284-9338C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170378949 | ||||||
| chr6:170379001
|
A | C | 1 | a0002c0003t0021g0113 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2284-9286A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170379001 | ||||||
| chr6:170379002
|
G | A | 1 | a0002c0003t0021g0113 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2284-9285G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170379002 | ||||||
| chr6:170379098
|
C | G | 36 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(33): Show | 36 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.2284-9189C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170379098 | ||||||
| chr6:170379755
|
C | T | 5 | a0001c0001t0001g0204a0001c0008t0001g0098a0001c0008t0001g0099others(2): Show | 5 | HG02738.hp2 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2284-8532C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170379755 | ||||||
| chr6:170379877
|
C | G | 1 | a0001c0001t0001g0262 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2284-8410C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170379877 | ||||||
| chr6:170379909
|
G | A | 6 | a0001c0002t0001g0102a0001c0002t0004g0104a0001c0008t0001g0098others(3): Show | 6 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2284-8378G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170379909 | ||||||
| chr6:170379932
|
G | A | 3 | a0001c0002t0010g0103a0001c0002t0013g0039a0001c0002t0013g0040 | 3 | HG01891.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2284-8355G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170379932 | ||||||
| chr6:170379950
|
C | T | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2284-8337C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170379950 | ||||||
| chr6:170380038
|
G | T | 46 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(43): Show | 48 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(45): Show |
intron_variant | MODIFIER | c.2284-8249G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170380038 | ||||||
| chr6:170380091
|
T | G | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2284-8196T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170380091 | ||||||
| chr6:170380516
|
C | G | 1 | a0001c0002t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2284-7771C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170380516 | ||||||
| chr6:170380532
|
C | T | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2284-7755C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170380532 | ||||||
| chr6:170380550
|
A | G | 156 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0013others(153): Show | 160 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.2284-7737A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170380550 | ||||||
| chr6:170380570
|
C | T | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2284-7717C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170380570 | ||||||
| chr6:170380594
|
G | C | 1 | a0001c0002t0004g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2284-7693G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170380594 | ||||||
| chr6:170380755
|
T | C | 46 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(43): Show | 47 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.2284-7532T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170380755 | ||||||
| chr6:170380871
|
A | T | 1 | a0002c0003t0021g0113 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2284-7416A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170380871 | ||||||
| chr6:170380913
|
A | G | 1 | a0001c0001t0008g0200 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2284-7374A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170380913 | ||||||
| chr6:170381027
|
T | A | 2 | a0006c0010t0010g0019a0006c0010t0010g0020 | 2 | HG01099.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2284-7260T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170381027 | ||||||
| chr6:170381055
|
A | T | 43 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(40): Show | 44 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(41): Show |
intron_variant | MODIFIER | c.2284-7232A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170381055 | ||||||
| chr6:170381094
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2284-7193G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170381094 | ||||||
| chr6:170381140
|
T | TTATGCTC others(23): Show |
1 | a0001c0002t0001g0053 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2284-7144_2284-711 others(34): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170381140 | |||||
| chr6:170381242
|
G | A | 3 | a0005c0007t0012g0002a0005c0007t0012g0003a0005c0007t0028g0003 | 4 | HG02055.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2284-7045G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170381242 | ||||||
| chr6:170381346
|
T | A | 2 | a0002c0003t0007g0112a0002c0003t0007g0145 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2284-6941T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170381346 | ||||||
| chr6:170381555
|
C | CA | 18 | a0001c0001t0001g0204a0001c0002t0001g0021a0001c0002t0001g0031others(15): Show | 18 | HG01069.hp2 HG01099.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.2284-6722dupA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170381555 | |||||
| chr6:170381600
|
T | C | 1 | a0002c0003t0021g0113 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2284-6687T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170381600 | ||||||
| chr6:170381608
|
G | A | 1 | a0001c0002t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2284-6679G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170381608 | ||||||
| chr6:170381795
|
C | T | 3 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014 | 3 | HG02280.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2284-6492C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170381795 | ||||||
| chr6:170381806
|
T | TA | 7 | a0001c0001t0005g0221a0001c0002t0001g0031a0001c0002t0001g0058others(4): Show | 7 | HG01069.hp2 HG01261.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.2284-6467dupA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170381806 | |||||
| chr6:170381820
|
A | G | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2284-6467A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170381820 | ||||||
| chr6:170381934
|
A | G | 45 | a0002c0003t0001g0134a0002c0003t0002g0004a0002c0003t0002g0106others(42): Show | 46 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.2284-6353A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170381934 | ||||||
| chr6:170381942
|
G | A | 10 | a0001c0001t0010g0083a0001c0001t0010g0095a0001c0001t0010g0096others(7): Show | 11 | HG02055.hp1 HG02717.hp1 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.2284-6345G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170381942 | ||||||
| chr6:170381984
|
A | G | 10 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0014others(7): Show | 10 | HG02280.hp1 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2284-6303A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170381984 | ||||||
| chr6:170381994
|
G | T | 16 | a0001c0001t0010g0095a0001c0001t0010g0096a0001c0002t0001g0024others(13): Show | 17 | HG00738.hp2 HG01081.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.2284-6293G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170381994 | ||||||
| chr6:170382354
|
T | C | 3 | a0001c0002t0013g0039a0001c0002t0013g0040a0009c0014t0009g0193 | 3 | HG01891.hp2 HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2284-5933T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170382354 | ||||||
| chr6:170382398
|
T | C | 8 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(5): Show | 8 | HG02572.hp2 HG02647.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.2284-5889T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170382398 | ||||||
| chr6:170382402
|
C | T | 166 | a0001c0001t0001g0207a0001c0001t0001g0272a0001c0001t0001g0273others(163): Show | 170 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(167): Show |
intron_variant | MODIFIER | c.2284-5885C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170382402 | ||||||
| chr6:170382634
|
TAAAAG | T | 41 | a0002c0003t0002g0004a0002c0003t0002g0106a0002c0003t0002g0108others(38): Show | 42 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.2284-5649_2284-564 others(9): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170382634 | |||||
| chr6:170382707
|
C | T | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2284-5580C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170382707 | ||||||
| chr6:170382836
|
C | A | 14 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0041others(11): Show | 14 | HG01069.hp2 HG01099.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2284-5451C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170382836 | ||||||
| chr6:170382844
|
A | G | 14 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0041others(11): Show | 14 | HG01069.hp2 HG01099.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2284-5443A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170382844 | ||||||
| chr6:170382902
|
A | G | 1 | a0001c0001t0010g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2284-5385A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170382902 | ||||||
| chr6:170382941
|
G | A | 18 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(15): Show | 19 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2284-5346G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170382941 | ||||||
| chr6:170382985
|
T | C | 2 | a0003c0004t0015g0151a0003c0004t0015g0155 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2284-5302T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170382985 | ||||||
| chr6:170382997
|
A | C | 2 | a0001c0008t0001g0098a0001c0008t0001g0099 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2284-5290A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170382997 | ||||||
| chr6:170383091
|
A | C | 1 | a0001c0001t0010g0096 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2284-5196A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170383091 | ||||||
| chr6:170383102
|
G | GA | 55 | a0001c0001t0010g0095a0001c0001t0010g0096a0001c0002t0001g0013others(52): Show | 56 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.2284-5170dupA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170383102 | |||||
| chr6:170383102
|
GA | G | 97 | a0001c0001t0001g0248a0001c0001t0009g0191a0001c0001t0009g0278others(94): Show | 99 | HG00099.hp1 HG00558.hp1 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.2284-5170delA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170383102 | |||||
| chr6:170383107
|
A | G | 18 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(15): Show | 19 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2284-5180A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170383107 | ||||||
| chr6:170383241
|
G | A | 1 | a0001c0002t0004g0179 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2284-5046G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170383241 | ||||||
| chr6:170383301
|
T | C | 4 | a0001c0002t0001g0013a0001c0002t0001g0102a0001c0009t0017g0093others(1): Show | 4 | HG02559.hp1 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2284-4986T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170383301 | ||||||
| chr6:170383419
|
A | C | 46 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(43): Show | 47 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(44): Show |
intron_variant | MODIFIER | c.2284-4868A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170383419 | ||||||
| chr6:170383419
|
A | G | 1 | a0004c0005t0001g0088 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2284-4868A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170383419 | ||||||
| chr6:170383440
|
T | C | 1 | a0001c0001t0006g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2284-4847T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170383440 | ||||||
| chr6:170383696
|
G | T | 1 | a0002c0003t0021g0113 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2284-4591G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170383696 | ||||||
| chr6:170383721
|
C | T | 46 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(43): Show | 47 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(44): Show |
intron_variant | MODIFIER | c.2284-4566C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170383721 | ||||||
| chr6:170383788
|
C | CATTTATC others(8): Show |
95 | a0001c0002t0001g0001a0001c0002t0001g0021a0001c0002t0001g0024others(92): Show | 97 | HG00099.hp1 HG00558.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.2284-4497_2284-449 others(19): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170383788 | |||||
| chr6:170383933
|
C | T | 6 | a0001c0001t0010g0095a0001c0001t0010g0096a0001c0002t0001g0067others(3): Show | 7 | HG02055.hp1 HG02451.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2284-4354C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170383933 | ||||||
| chr6:170384185
|
G | T | 1 | a0002c0003t0002g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2284-4102G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170384185 | ||||||
| chr6:170384238
|
G | A | 3 | a0001c0001t0005g0213a0001c0001t0005g0214a0001c0001t0005g0221 | 3 | HG00639.hp2 HG01109.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2284-4049G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170384238 | ||||||
| chr6:170384348
|
C | T | 268 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(265): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.2284-3939C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170384348 | ||||||
| chr6:170384434
|
G | T | 4 | a0001c0002t0001g0013a0001c0002t0001g0102a0001c0009t0017g0093others(1): Show | 4 | HG02559.hp1 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2284-3853G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170384434 | ||||||
| chr6:170384590
|
G | A | 7 | a0001c0001t0010g0083a0001c0002t0001g0012a0001c0002t0001g0014others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2284-3697G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170384590 | ||||||
| chr6:170384673
|
A | G | 10 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0041others(7): Show | 10 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2284-3614A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170384673 | ||||||
| chr6:170384775
|
A | G | 1 | a0001c0002t0004g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2284-3512A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170384775 | ||||||
| chr6:170384996
|
T | C | 110 | a0001c0001t0002g0244a0001c0001t0019g0211a0001c0002t0001g0001others(107): Show | 112 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.2284-3291T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170384996 | ||||||
| chr6:170385002
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2284-3285C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170385002 | ||||||
| chr6:170385036
|
A | G | 145 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(142): Show | 148 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.2284-3251A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170385036 | ||||||
| chr6:170385081
|
T | C | 1 | a0001c0002t0011g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2284-3206T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170385081 | ||||||
| chr6:170385214
|
A | G | 1 | a0001c0002t0011g0017 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2284-3073A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170385214 | ||||||
| chr6:170385319
|
G | T | 1 | a0001c0001t0005g0208 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2284-2968G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170385319 | ||||||
| chr6:170385369
|
TA | T | 48 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0014others(45): Show | 49 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(46): Show |
intron_variant | MODIFIER | c.2284-2910delA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 170385369 | |||||
| chr6:170385426
|
A | G | 2 | a0006c0010t0010g0019a0006c0010t0010g0020 | 2 | HG01099.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2284-2861A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170385426 | ||||||
| chr6:170385520
|
T | A | 17 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(14): Show | 17 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.2284-2767T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170385520 | ||||||
| chr6:170385572
|
A | C | 244 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(241): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.2284-2715A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170385572 | ||||||
| chr6:170385654
|
C | A | 11 | a0001c0001t0001g0011a0001c0001t0001g0229a0001c0001t0001g0239others(8): Show | 12 | HG02280.hp2 HG02572.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.2284-2633C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170385654 | ||||||
| chr6:170385675
|
T | C | 1 | a0003c0004t0003g0154 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2284-2612T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170385675 | ||||||
| chr6:170385715
|
C | T | 50 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0014others(47): Show | 51 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(48): Show |
intron_variant | MODIFIER | c.2284-2572C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170385715 | ||||||
| chr6:170385767
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0239a0001c0001t0001g0240others(1): Show | 5 | HG02280.hp2 HG02717.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2284-2520G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170385767 | ||||||
| chr6:170385956
|
A | C | 251 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(248): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.2284-2331A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170385956 | ||||||
| chr6:170386294
|
T | G | 1 | a0001c0002t0001g0097 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2284-1993T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170386294 | ||||||
| chr6:170386437
|
A | T | 1 | a0001c0001t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2284-1850A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170386437 | ||||||
| chr6:170386876
|
G | A | 1 | a0003c0004t0003g0159 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2284-1411G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170386876 | ||||||
| chr6:170387134
|
G | A | 128 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(125): Show | 130 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.2284-1153G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170387134 | ||||||
| chr6:170387284
|
G | T | 6 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(3): Show | 6 | HG00280.hp2 HG01074.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.2284-1003G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170387284 | ||||||
| chr6:170387297
|
A | G | 129 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(126): Show | 131 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.2284-990A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170387297 | ||||||
| chr6:170387442
|
C | T | 3 | a0002c0003t0002g0128a0002c0003t0002g0131a0002c0003t0002g0132 | 3 | HG01255.hp2 HG01256.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.2284-845C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170387442 | ||||||
| chr6:170387644
|
A | G | 2 | a0001c0002t0013g0039a0001c0002t0013g0040 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2284-643A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170387644 | ||||||
| chr6:170387677
|
A | T | 1 | a0001c0001t0001g0269 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2284-610A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170387677 | ||||||
| chr6:170387752
|
A | G | 2 | a0001c0001t0005g0208a0001c0001t0005g0224 | 2 | HG02004.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2284-535A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170387752 | ||||||
| chr6:170387937
|
A | G | 238 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(235): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.2284-350A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170387937 | ||||||
| chr6:170388056
|
A | G | 4 | a0001c0002t0001g0001a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 5 | NA18939.hp2 NA18942.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.2284-231A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170388056 | ||||||
| chr6:170388111
|
G | T | 244 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(241): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.2284-176G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | chr6 | 170388111 | ||||||
| chr6:170388941
|
A | T | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2490+448A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/10 | chr6 | 170388941 | ||||||
| chr6:170389026
|
A | G | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2490+533A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/10 | chr6 | 170389026 | ||||||
| chr6:170389171
|
A | G | 4 | a0003c0004t0003g0157a0003c0004t0003g0158a0003c0004t0003g0163others(1): Show | 4 | HG01978.hp2 NA18970.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.2490+678A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/10 | chr6 | 170389171 | ||||||
| chr6:170389207
|
A | G | 2 | a0001c0001t0002g0244a0001c0001t0019g0211 | 2 | HG02300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2490+714A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/10 | chr6 | 170389207 | ||||||
| chr6:170389396
|
T | C | 1 | a0001c0001t0010g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2490+903T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/10 | chr6 | 170389396 | ||||||
| chr6:170389425
|
A | G | 244 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(241): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.2490+932A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/10 | chr6 | 170389425 | ||||||
| chr6:170389579
|
A | G | 244 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(241): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.2490+1086A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/10 | chr6 | 170389579 | ||||||
| chr6:170389705
|
G | A | 1 | a0001c0001t0010g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2490+1212G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/10 | chr6 | 170389705 | ||||||
| chr6:170389906
|
G | A | 2 | a0001c0008t0001g0098a0001c0008t0001g0099 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2491-1107G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/10 | chr6 | 170389906 | ||||||
| chr6:170390175
|
C | A | 10 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0041others(7): Show | 10 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2491-838C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/10 | chr6 | 170390175 | ||||||
| chr6:170390276
|
G | A | 4 | a0001c0002t0001g0013a0001c0002t0001g0102a0001c0009t0017g0093others(1): Show | 4 | HG02559.hp1 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2491-737G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/10 | chr6 | 170390276 | ||||||
| chr6:170390479
|
A | G | 44 | a0001c0001t0002g0244a0001c0001t0019g0211a0002c0003t0002g0004others(41): Show | 45 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.2491-534A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/10 | chr6 | 170390479 | ||||||
| chr6:170390610
|
G | A | 5 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(2): Show | 6 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2491-403G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/10 | chr6 | 170390610 | ||||||
| chr6:170390624
|
T | G | 244 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(241): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.2491-389T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/10 | chr6 | 170390624 | ||||||
| chr6:170390648
|
G | A | 1 | a0002c0003t0002g0130 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2491-365G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/10 | chr6 | 170390648 | ||||||
| chr6:170390822
|
T | C | 1 | a0001c0001t0005g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2491-191T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/10 | chr6 | 170390822 | ||||||
| chr6:170390834
|
G | A | 17 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(14): Show | 17 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.2491-179G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 7/10 | chr6 | 170390834 | ||||||
| chr6:170391164
|
A | C | 1 | a0001c0001t0001g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2599+43A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170391164 | ||||||
| chr6:170391338
|
C | T | 3 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0001g0038 | 3 | HG02615.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2599+217C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170391338 | ||||||
| chr6:170391394
|
G | A | 8 | a0001c0008t0001g0098a0001c0008t0001g0099a0004c0005t0001g0084others(5): Show | 8 | HG02886.hp1 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.2599+273G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170391394 | ||||||
| chr6:170391408
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2599+287G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170391408 | ||||||
| chr6:170391510
|
A | G | 279 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(276): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.2599+389A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170391510 | ||||||
| chr6:170391546
|
A | G | 2 | a0001c0002t0001g0013a0001c0002t0001g0102 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2599+425A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170391546 | ||||||
| chr6:170391687
|
A | G | 244 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(241): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.2599+566A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170391687 | ||||||
| chr6:170391950
|
C | T | 4 | a0001c0002t0001g0046a0001c0002t0001g0047a0001c0002t0001g0049others(1): Show | 4 | NA19068.hp1 NA19074.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.2599+829C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170391950 | ||||||
| chr6:170392106
|
A | G | 245 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(242): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.2599+985A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170392106 | ||||||
| chr6:170392113
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2599+992A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170392113 | ||||||
| chr6:170392124
|
A | G | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2599+1003A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170392124 | ||||||
| chr6:170392293
|
C | T | 1 | a0001c0001t0008g0200 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2599+1172C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170392293 | ||||||
| chr6:170392294
|
G | A | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2599+1173G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170392294 | ||||||
| chr6:170392332
|
C | T | 10 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0041others(7): Show | 10 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2599+1211C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170392332 | ||||||
| chr6:170392352
|
C | T | 6 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(3): Show | 6 | HG00280.hp2 HG01074.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.2599+1231C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170392352 | ||||||
| chr6:170392364
|
C | T | 1 | a0001c0001t0025g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2599+1243C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170392364 | ||||||
| chr6:170392734
|
G | A | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2599+1613G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170392734 | ||||||
| chr6:170392743
|
G | C | 4 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0241others(1): Show | 4 | HG01243.hp1 HG01891.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2599+1622G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170392743 | ||||||
| chr6:170393032
|
C | T | 1 | a0001c0001t0009g0278 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2599+1911C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170393032 | ||||||
| chr6:170393072
|
C | G | 36 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(33): Show | 42 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.2599+1951C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170393072 | ||||||
| chr6:170393114
|
C | G | 2 | a0001c0001t0016g0198a0001c0001t0016g0199 | 2 | HG01123.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.2599+1993C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170393114 | ||||||
| chr6:170393148
|
C | CA | 55 | a0001c0002t0001g0021a0001c0002t0001g0024a0001c0002t0001g0031others(52): Show | 56 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.2599+2045dupA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170393148 | |||||
| chr6:170393148
|
C | CAA | 92 | a0001c0001t0001g0011a0001c0001t0001g0207a0001c0001t0001g0227others(89): Show | 93 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.2599+2044_2599+204 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170393148 | |||||
| chr6:170393148
|
C | CAAA | 6 | a0001c0001t0001g0204a0001c0001t0001g0245a0001c0001t0001g0250others(3): Show | 6 | HG01261.hp2 HG02738.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.2599+2043_2599+204 others(7): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170393148 | |||||
| chr6:170393148
|
CA | C | 34 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(31): Show | 39 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.2599+2045delA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170393148 | |||||
| chr6:170393292
|
C | T | 1 | a0001c0002t0010g0103 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2599+2171C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170393292 | ||||||
| chr6:170393362
|
T | G | 1 | a0001c0001t0008g0271 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2600-2125T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170393362 | ||||||
| chr6:170393414
|
A | G | 235 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(232): Show | 244 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.2600-2073A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170393414 | ||||||
| chr6:170393415
|
C | T | 233 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(230): Show | 242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.2600-2072C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170393415 | ||||||
| chr6:170393483
|
T | C | 1 | a0001c0002t0004g0022 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2600-2004T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170393483 | ||||||
| chr6:170393765
|
C | T | 1 | a0002c0003t0002g0140 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2600-1722C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170393765 | ||||||
| chr6:170393838
|
C | T | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2600-1649C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170393838 | ||||||
| chr6:170393916
|
A | ACT | 39 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(36): Show | 45 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.2600-1569_2600-156 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170393916 | |||||
| chr6:170394042
|
C | T | 21 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(18): Show | 21 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.2600-1445C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170394042 | ||||||
| chr6:170394417
|
G | GTGCCAGC others(107): Show |
1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2600-1053_2600-105 others(118): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394417 | |||||
| chr6:170394417
|
G | GTGCCAGC others(69): Show |
2 | a0005c0007t0012g0003a0005c0007t0028g0003 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2600-1053_2600-105 others(80): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394417 | |||||
| chr6:170394417
|
G | GTGCCAGC others(183): Show |
1 | a0001c0001t0010g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2600-1053_2600-105 others(194): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394417 | |||||
| chr6:170394417
|
G | GTGCCAGC others(221): Show |
1 | a0001c0002t0007g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2600-1053_2600-105 others(232): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394417 | |||||
| chr6:170394417
|
G | GTGCCAGC others(145): Show |
2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2600-1053_2600-105 others(156): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394417 | |||||
| chr6:170394417
|
G | GTGCCAGC others(183): Show |
1 | a0005c0007t0012g0002 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2600-1053_2600-105 others(194): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394417 | |||||
| chr6:170394417
|
G | GTGCCAGC others(221): Show |
12 | a0001c0001t0009g0009a0001c0001t0009g0189a0001c0001t0009g0190others(9): Show | 15 | HG00733.hp2 HG01109.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.2600-1053_2600-105 others(232): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394417 | |||||
| chr6:170394417
|
G | GTGCCAGC others(259): Show |
11 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(8): Show | 12 | HG01123.hp1 HG01243.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.2600-1053_2600-105 others(270): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394417 | |||||
| chr6:170394417
|
G | GTGCCAGC others(31): Show |
19 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(16): Show | 19 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.2600-908_2600-871d others(40): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394417 | |||||
| chr6:170394417
|
G | GTGCCAGC others(69): Show |
7 | a0001c0002t0010g0103a0004c0005t0001g0084a0004c0005t0001g0085others(4): Show | 7 | HG02809.hp1 HG02965.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2600-946_2600-871d others(78): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394417 | |||||
| chr6:170394417
|
G | GTGCCAGC others(107): Show |
30 | a0001c0001t0001g0204a0001c0001t0001g0245a0001c0001t0001g0247others(27): Show | 30 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.2600-984_2600-871d others(116): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394417 | |||||
| chr6:170394417
|
G | GTGCCAGC others(183): Show |
1 | a0001c0002t0029g0091 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2600-924_2600-923i others(192): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394417 | |||||
| chr6:170394417
|
G | GTGCCAGC others(145): Show |
2 | a0001c0008t0001g0098a0001c0008t0001g0099 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2600-1022_2600-871 others(155): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394417 | |||||
| chr6:170394434
|
C | CACCTCCG others(183): Show |
4 | a0001c0002t0007g0006a0001c0002t0007g0184a0001c0002t0007g0185others(1): Show | 5 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.2600-1053_2600-105 others(194): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170394434 | ||||||
| chr6:170394440
|
C | CGTGGACA others(31): Show |
2 | a0006c0010t0010g0019a0006c0010t0010g0020 | 2 | HG01099.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2600-1010_2600-100 others(42): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394440 | |||||
| chr6:170394465
|
A | AAGGCCAC others(31): Show |
2 | a0001c0002t0001g0057a0001c0002t0001g0058 | 2 | NA18970.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2600-985_2600-984i others(40): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394465 | |||||
| chr6:170394465
|
A | AAGGCCAC others(69): Show |
2 | a0001c0002t0011g0016a0001c0002t0011g0017 | 2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2600-985_2600-984i others(78): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394465 | |||||
| chr6:170394503
|
A | AAGGCCAC others(31): Show |
6 | a0003c0004t0003g0005a0003c0004t0003g0166a0003c0004t0003g0167others(3): Show | 7 | NA18942.hp1 NA18944.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.2600-947_2600-946i others(40): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394503 | |||||
| chr6:170394503
|
A | AAGGCCAC others(69): Show |
1 | a0001c0002t0011g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2600-947_2600-946i others(78): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394503 | |||||
| chr6:170394503
|
A | AAGGCCAC others(107): Show |
1 | a0011c0011t0001g0129 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2600-947_2600-946i others(116): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394503 | |||||
| chr6:170394503
|
A | G | 6 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0079others(3): Show | 6 | HG02615.hp1 HG02818.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.2600-984A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170394503 | ||||||
| chr6:170394511
|
G | GCCTCCGT others(107): Show |
1 | a0001c0001t0001g0261 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2600-871_2600-870i others(116): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394511 | |||||
| chr6:170394541
|
A | AAGGCCAC others(69): Show |
4 | a0001c0002t0001g0015a0001c0002t0001g0073a0001c0002t0001g0074others(1): Show | 4 | HG06807.hp1 NA18942.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.2600-909_2600-908i others(78): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394541 | |||||
| chr6:170394541
|
A | AAGGCCAC others(107): Show |
4 | a0001c0002t0001g0050a0001c0002t0001g0054a0001c0002t0001g0060others(1): Show | 4 | HG03927.hp1 NA18944.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2600-909_2600-908i others(116): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394541 | |||||
| chr6:170394541
|
A | G | 31 | a0001c0002t0001g0012a0001c0002t0001g0014a0001c0002t0001g0057others(28): Show | 32 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.2600-946A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170394541 | ||||||
| chr6:170394564
|
G | A | 1 | a0001c0002t0001g0063 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2600-923G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170394564 | ||||||
| chr6:170394579
|
A | AAGGCCAC others(31): Show |
3 | a0002c0003t0002g0137a0006c0010t0010g0019a0006c0010t0010g0020 | 3 | HG01099.hp1 HG02970.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.2600-839_2600-802d others(40): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394579 | |||||
| chr6:170394579
|
A | AAGGCCAC others(107): Show |
32 | a0001c0002t0001g0001a0001c0002t0001g0036a0001c0002t0001g0037others(29): Show | 33 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(30): Show |
intron_variant | MODIFIER | c.2600-802_2600-801i others(116): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394579 | |||||
| chr6:170394579
|
A | AAGGCCAC others(145): Show |
1 | a0001c0002t0001g0071 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2600-802_2600-801i others(154): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394579 | |||||
| chr6:170394579
|
A | G | 40 | a0001c0002t0001g0012a0001c0002t0001g0014a0001c0002t0001g0015others(37): Show | 41 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.2600-908A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170394579 | ||||||
| chr6:170394617
|
G | A | 160 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(157): Show | 167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.2600-870G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170394617 | ||||||
| chr6:170394624
|
C | CGCCTCCG others(69): Show |
2 | a0001c0002t0001g0012a0001c0002t0001g0014 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2600-802_2600-801i others(78): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394624 | |||||
| chr6:170394630
|
C | CGTGGACA others(145): Show |
53 | a0001c0001t0001g0207a0001c0001t0001g0227a0001c0001t0001g0228others(50): Show | 53 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.2600-833_2600-832i others(154): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394630 | |||||
| chr6:170394630
|
C | CGTGGACA others(69): Show |
4 | a0001c0001t0001g0011a0001c0001t0001g0239a0001c0001t0001g0240others(1): Show | 5 | HG02280.hp2 HG02717.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2600-833_2600-832i others(78): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394630 | |||||
| chr6:170394655
|
G | A | 143 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(140): Show | 150 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.2600-832G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170394655 | ||||||
| chr6:170394662
|
CGCCTCCG others(31): Show |
C | 1 | a0001c0002t0001g0079 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2600-799_2600-762d others(40): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr6 | 170394662 | |||||
| chr6:170394677
|
C | T | 1 | a0003c0004t0003g0164 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2600-810C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170394677 | ||||||
| chr6:170394686
|
T | C | 7 | a0001c0001t0010g0095a0001c0001t0010g0096a0001c0002t0001g0059others(4): Show | 8 | HG01433.hp2 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2600-801T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170394686 | ||||||
| chr6:170394693
|
A | G | 41 | a0001c0002t0001g0001a0001c0002t0001g0046a0001c0002t0001g0047others(38): Show | 42 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(39): Show |
intron_variant | MODIFIER | c.2600-794A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170394693 | ||||||
| chr6:170394700
|
T | C | 234 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(231): Show | 243 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.2600-787T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170394700 | ||||||
| chr6:170394726
|
C | T | 6 | a0004c0005t0001g0084a0004c0005t0001g0085a0004c0005t0001g0086others(3): Show | 6 | HG02965.hp2 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2600-761C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170394726 | ||||||
| chr6:170394752
|
C | T | 1 | a0001c0001t0005g0249 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2600-735C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170394752 | ||||||
| chr6:170394820
|
C | T | 21 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(18): Show | 21 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.2600-667C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170394820 | ||||||
| chr6:170394857
|
C | T | 88 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(85): Show | 89 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.2600-630C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170394857 | ||||||
| chr6:170394912
|
G | A | 3 | a0001c0001t0001g0231a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | HG01074.hp1 HG01255.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2600-575G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170394912 | ||||||
| chr6:170395007
|
A | G | 1 | a0011c0011t0001g0129 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2600-480A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170395007 | ||||||
| chr6:170395027
|
C | G | 10 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0041others(7): Show | 10 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2600-460C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170395027 | ||||||
| chr6:170395052
|
C | T | 266 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(263): Show | 275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.2600-435C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170395052 | ||||||
| chr6:170395108
|
C | G | 96 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(93): Show | 97 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.2600-379C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170395108 | ||||||
| chr6:170395131
|
A | C | 62 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(59): Show | 68 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.2600-356A>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170395131 | ||||||
| chr6:170395190
|
G | A | 1 | a0001c0001t0006g0220 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2600-297G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170395190 | ||||||
| chr6:170395268
|
C | A | 96 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(93): Show | 97 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.2600-219C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170395268 | ||||||
| chr6:170395290
|
G | T | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2600-197G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170395290 | ||||||
| chr6:170395356
|
C | A | 185 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(182): Show | 193 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.2600-131C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 8/10 | chr6 | 170395356 | ||||||
| chr6:170395858
|
G | C | 129 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(126): Show | 131 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.2692+279G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170395858 | ||||||
| chr6:170395913
|
G | T | 10 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0041others(7): Show | 10 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2692+334G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170395913 | ||||||
| chr6:170396020
|
C | T | 5 | a0001c0001t0010g0095a0001c0001t0010g0096a0005c0007t0012g0002others(2): Show | 6 | HG02055.hp1 HG02451.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2692+441C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170396020 | ||||||
| chr6:170396021
|
A | G | 34 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(31): Show | 40 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.2692+442A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170396021 | ||||||
| chr6:170396133
|
T | C | 2 | a0001c0001t0010g0095a0001c0001t0010g0096 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2692+554T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170396133 | ||||||
| chr6:170396199
|
A | G | 6 | a0004c0005t0001g0084a0004c0005t0001g0085a0004c0005t0001g0086others(3): Show | 6 | HG02965.hp2 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2692+620A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170396199 | ||||||
| chr6:170396230
|
T | C | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2692+651T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170396230 | ||||||
| chr6:170396294
|
C | T | 1 | a0001c0002t0030g0182 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2692+715C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170396294 | ||||||
| chr6:170396349
|
G | A | 1 | a0006c0010t0010g0019 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2692+770G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170396349 | ||||||
| chr6:170396431
|
A | G | 1 | a0001c0001t0010g0095 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2692+852A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170396431 | ||||||
| chr6:170396440
|
T | C | 2 | a0001c0001t0001g0245a0001c0001t0001g0250 | 2 | HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2692+861T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170396440 | ||||||
| chr6:170396581
|
A | G | 3 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0082 | 3 | NA18942.hp2 NA18964.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2692+1002A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170396581 | ||||||
| chr6:170396584
|
C | G | 1 | a0001c0002t0001g0035 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2692+1005C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170396584 | ||||||
| chr6:170396700
|
G | A | 1 | a0001c0001t0008g0200 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2692+1121G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170396700 | ||||||
| chr6:170396907
|
T | G | 1 | a0002c0003t0002g0108 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2692+1328T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170396907 | ||||||
| chr6:170397085
|
C | G | 1 | a0001c0001t0001g0204 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2692+1506C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170397085 | ||||||
| chr6:170397106
|
C | A | 84 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(81): Show | 85 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.2692+1527C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170397106 | ||||||
| chr6:170397507
|
G | C | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2692+1928G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170397507 | ||||||
| chr6:170397581
|
G | C | 1 | a0001c0001t0001g0251 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2692+2002G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170397581 | ||||||
| chr6:170397607
|
C | G | 1 | a0001c0002t0007g0007 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2692+2028C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170397607 | ||||||
| chr6:170397642
|
G | C | 21 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(18): Show | 21 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.2692+2063G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170397642 | ||||||
| chr6:170397686
|
T | G | 2 | a0001c0002t0001g0037a0001c0002t0001g0038 | 2 | HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2692+2107T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170397686 | ||||||
| chr6:170397841
|
C | T | 1 | a0001c0001t0008g0192 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2692+2262C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170397841 | ||||||
| chr6:170397850
|
G | A | 10 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(7): Show | 11 | HG01123.hp1 HG01243.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.2692+2271G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170397850 | ||||||
| chr6:170397937
|
C | T | 21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2692+2358C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170397937 | ||||||
| chr6:170397982
|
GC | G | 96 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(93): Show | 97 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.2692+2404delC | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170397982 | ||||||
| chr6:170398116
|
G | C | 6 | a0001c0002t0001g0012a0001c0002t0001g0014a0001c0002t0001g0015others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.2692+2537G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398116 | ||||||
| chr6:170398173
|
G | A | 1 | a0001c0002t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2692+2594G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398173 | ||||||
| chr6:170398207
|
G | A | 8 | a0001c0008t0001g0098a0001c0008t0001g0099a0004c0005t0001g0084others(5): Show | 8 | HG02886.hp1 HG02965.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.2692+2628G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398207 | ||||||
| chr6:170398265
|
T | C | 84 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(81): Show | 85 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.2692+2686T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398265 | ||||||
| chr6:170398292
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2692+2713A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398292 | ||||||
| chr6:170398336
|
A | G | 5 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(2): Show | 6 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2692+2757A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398336 | ||||||
| chr6:170398396
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2692+2817G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398396 | ||||||
| chr6:170398432
|
T | G | 3 | a0001c0001t0005g0205a0001c0001t0005g0258a0001c0001t0020g0206 | 3 | HG01192.hp2 HG01934.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2692+2853T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398432 | ||||||
| chr6:170398457
|
G | C | 1 | a0005c0007t0012g0002 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2692+2878G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398457 | ||||||
| chr6:170398507
|
G | A | 2 | a0004c0005t0001g0085a0004c0005t0001g0089 | 2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2692+2928G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398507 | ||||||
| chr6:170398514
|
G | A | 2 | a0001c0008t0001g0098a0001c0008t0001g0099 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2692+2935G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398514 | ||||||
| chr6:170398534
|
ACTCTTAG others(732): Show |
A | 1 | a0005c0007t0012g0002 | 2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2692+2958_2692+369 others(4): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398534 | |||||
| chr6:170398551
|
A | G | 21 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(18): Show | 21 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.2692+2972A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398551 | ||||||
| chr6:170398553
|
A | AAAGGTAG others(6710): Show |
1 | a0001c0001t0006g0201 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2692+3038_2692+303 others(6721): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398553 | |||||
| chr6:170398553
|
A | AAAGGTAG others(6480): Show |
1 | a0001c0001t0005g0214 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2692+3038_2692+303 others(6491): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398553 | |||||
| chr6:170398553
|
A | AAAGGTAG others(8344): Show |
1 | a0001c0001t0001g0277 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2692+3038_2692+303 others(8355): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398553 | |||||
| chr6:170398553
|
A | AAAGGTAG others(5004): Show |
1 | a0001c0001t0001g0240 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2692+3038_2692+303 others(5015): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398553 | |||||
| chr6:170398553
|
A | AAAGGTAG others(8344): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0239 | 3 | HG02280.hp2 HG02717.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2692+3038_2692+303 others(8355): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398553 | |||||
| chr6:170398553
|
A | AAAGGTAG others(10555): Show |
2 | a0001c0001t0001g0234a0001c0001t0001g0242 | 2 | HG01243.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2692+3038_2692+303 others(10566): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398553 | |||||
| chr6:170398553
|
A | AAAGGTAG others(11489): Show |
1 | a0001c0018t0006g0215 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2692+3038_2692+303 others(11500): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398553 | |||||
| chr6:170398553
|
A | AAAGGTAG others(8344): Show |
1 | a0001c0001t0005g0258 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2692+3038_2692+303 others(8355): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398553 | |||||
| chr6:170398553
|
A | AAAGGTAG others(5004): Show |
1 | a0001c0001t0006g0203 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2692+3038_2692+303 others(5015): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398553 | |||||
| chr6:170398553
|
A | AAAGGTAG others(6826): Show |
1 | a0001c0001t0014g0212 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2692+3038_2692+303 others(6837): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398553 | |||||
| chr6:170398553
|
A | AAAGGTAG others(3370): Show |
1 | a0001c0001t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2692+3038_2692+303 others(3381): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398553 | |||||
| chr6:170398553
|
A | AAAGGTAG others(10093): Show |
1 | a0001c0006t0001g0246 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2692+3038_2692+303 others(10104): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398553 | |||||
| chr6:170398553
|
A | AAAGGTAG others(9237): Show |
1 | a0001c0001t0001g0260 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2692+3038_2692+303 others(9248): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398553 | |||||
| chr6:170398559
|
A | G | 1 | a0001c0002t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2692+2980A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398559 | ||||||
| chr6:170398563
|
C | T | 2 | a0005c0007t0012g0003a0005c0007t0028g0003 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2692+2984C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398563 | ||||||
| chr6:170398574
|
G | C | 54 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(51): Show | 59 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.2692+2995G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398574 | ||||||
| chr6:170398575
|
C | CCTTAGGA others(11684): Show |
1 | a0001c0002t0001g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2692+3038_2692+303 others(11695): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398575 | |||||
| chr6:170398575
|
C | CCTTAGGA others(30): Show |
1 | a0001c0001t0010g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2692+3024_2692+302 others(41): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398575 | |||||
| chr6:170398575
|
C | T | 21 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(18): Show | 21 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.2692+2996C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398575 | ||||||
| chr6:170398589
|
G | GGGGAAGG others(5001): Show |
1 | a0001c0001t0005g0217 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2692+3038_2692+303 others(5012): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398589 | |||||
| chr6:170398609
|
T | A | 54 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(51): Show | 59 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.2692+3030T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398609 | ||||||
| chr6:170398614
|
T | TCTTAGGA others(30): Show |
30 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(27): Show | 35 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2692+3038_2692+303 others(41): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398614 | |||||
| chr6:170398617
|
T | TAG | 49 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0014others(46): Show | 50 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(47): Show |
intron_variant | MODIFIER | c.2692+3038_2692+303 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398617 | ||||||
| chr6:170398618
|
C | A | 185 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(182): Show | 192 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.2692+3039C>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398618 | ||||||
| chr6:170398618
|
C | G | 49 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0014others(46): Show | 50 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(47): Show |
intron_variant | MODIFIER | c.2692+3039C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398618 | ||||||
| chr6:170398620
|
GAGTGAGT others(340): Show |
G | 1 | a0001c0002t0001g0094 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2692+3042_2692+338 others(4): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398620 | ||||||
| chr6:170398631
|
A | G | 22 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(19): Show | 22 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2692+3052A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398631 | ||||||
| chr6:170398653
|
T | TCTTAGGA others(110): Show |
1 | a0001c0002t0001g0056 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2692+3158_2692+327 others(121): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398653 | |||||
| chr6:170398668
|
G | A | 51 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(48): Show | 56 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.2692+3089G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398668 | ||||||
| chr6:170398670
|
G | A | 52 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(49): Show | 57 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.2692+3091G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398670 | ||||||
| chr6:170398670
|
G | GAAGGTAG others(303): Show |
1 | a0001c0001t0001g0231 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2692+3127_2692+312 others(314): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398670 | |||||
| chr6:170398670
|
G | GAAGGTAG others(303): Show |
1 | a0001c0001t0005g0224 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2692+3127_2692+312 others(314): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398670 | |||||
| chr6:170398670
|
G | GAAGGTAG others(303): Show |
65 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0227others(62): Show | 65 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.2692+3127_2692+312 others(314): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398670 | |||||
| chr6:170398683
|
T | C | 20 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(17): Show | 20 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.2692+3104T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398683 | ||||||
| chr6:170398691
|
C | G | 20 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(17): Show | 20 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.2692+3112C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398691 | ||||||
| chr6:170398692
|
T | C | 20 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(17): Show | 20 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.2692+3113T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398692 | ||||||
| chr6:170398709
|
G | A | 2 | a0005c0007t0012g0003a0005c0007t0028g0003 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2692+3130G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398709 | ||||||
| chr6:170398746
|
A | G | 88 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0227others(85): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.2692+3167A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398746 | ||||||
| chr6:170398748
|
A | G | 88 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0227others(85): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.2692+3169A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398748 | ||||||
| chr6:170398761
|
C | T | 121 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0227others(118): Show | 126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.2692+3182C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398761 | ||||||
| chr6:170398769
|
G | C | 121 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0227others(118): Show | 126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.2692+3190G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398769 | ||||||
| chr6:170398770
|
C | T | 121 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0227others(118): Show | 126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.2692+3191C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398770 | ||||||
| chr6:170398776
|
G | A | 20 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(17): Show | 20 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.2692+3197G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398776 | ||||||
| chr6:170398784
|
G | T | 41 | a0001c0001t0001g0011a0001c0001t0001g0234a0001c0001t0001g0239others(38): Show | 42 | HG00323.hp2 HG00639.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.2692+3205G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398784 | ||||||
| chr6:170398785
|
G | A | 68 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0227others(65): Show | 68 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.2692+3206G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398785 | ||||||
| chr6:170398787
|
G | A | 88 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0227others(85): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.2692+3208G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398787 | ||||||
| chr6:170398807
|
ACT | A | 88 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0227others(85): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.2692+3231_2692+323 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398807 | |||||
| chr6:170398809
|
T | TCGTAGGA others(340): Show |
3 | a0001c0002t0013g0039a0001c0002t0013g0040a0001c0002t0029g0091 | 3 | HG01891.hp2 HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2692+3231_2692+323 others(351): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398809 | |||||
| chr6:170398809
|
T | TCTTAGGA others(340): Show |
1 | a0001c0001t0001g0277 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2692+3268_2692+326 others(351): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398809 | |||||
| chr6:170398809
|
T | TCTTAGGA others(379): Show |
1 | a0001c0001t0001g0260 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2692+3383_2692+338 others(390): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398809 | |||||
| chr6:170398809
|
T | TCTTAGGA others(301): Show |
4 | a0001c0001t0005g0258a0001c0001t0006g0201a0001c0001t0014g0212others(1): Show | 4 | HG00323.hp2 HG03710.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.2692+3515_2692+351 others(312): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398809 | |||||
| chr6:170398809
|
T | TCTTAGGA others(1469): Show |
2 | a0001c0001t0001g0234a0001c0001t0001g0242 | 2 | HG01243.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2692+3515_2692+351 others(1480): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398809 | |||||
| chr6:170398809
|
T | TCTTAGGA others(340): Show |
25 | a0001c0001t0001g0011a0001c0001t0001g0239a0001c0002t0001g0032others(22): Show | 27 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.2692+3309_2692+365 others(351): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398809 | |||||
| chr6:170398809
|
T | TCTTAGGA others(340): Show |
10 | a0001c0002t0001g0013a0001c0002t0001g0102a0001c0009t0017g0093others(7): Show | 10 | HG02559.hp1 HG02965.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.2692+3359_2692+336 others(351): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398809 | |||||
| chr6:170398811
|
T | G | 9 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0041others(6): Show | 9 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2692+3232T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398811 | ||||||
| chr6:170398824
|
G | A | 2 | a0005c0007t0012g0003a0005c0007t0028g0003 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2692+3245G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398824 | ||||||
| chr6:170398826
|
G | A | 22 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(19): Show | 22 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2692+3247G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398826 | ||||||
| chr6:170398848
|
T | C | 20 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(17): Show | 20 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.2692+3269T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398848 | ||||||
| chr6:170398854
|
A | G | 53 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(50): Show | 58 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.2692+3275A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398854 | ||||||
| chr6:170398863
|
G | A | 51 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(48): Show | 56 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.2692+3284G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398863 | ||||||
| chr6:170398865
|
A | G | 2 | a0005c0007t0012g0003a0005c0007t0028g0003 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2692+3286A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398865 | ||||||
| chr6:170398878
|
T | C | 31 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(28): Show | 36 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.2692+3299T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398878 | ||||||
| chr6:170398881
|
C | T | 9 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0041others(6): Show | 9 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2692+3302C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398881 | ||||||
| chr6:170398885
|
A | ACT | 23 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(20): Show | 23 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.2692+3307_2692+330 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398885 | |||||
| chr6:170398885
|
A | AGC | 31 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(28): Show | 36 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.2692+3306_2692+330 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398885 | ||||||
| chr6:170398900
|
G | A | 1 | a0001c0002t0004g0025 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2692+3321G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398900 | ||||||
| chr6:170398901
|
G | GAAAGGTA others(340): Show |
2 | a0001c0001t0001g0240a0001c0001t0005g0217 | 2 | HG01257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2692+3655_2692+365 others(351): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398901 | |||||
| chr6:170398901
|
G | GAAAGGTA others(340): Show |
1 | a0001c0001t0005g0214 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2692+3557_2692+355 others(351): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398901 | |||||
| chr6:170398902
|
A | G | 33 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(30): Show | 38 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.2692+3323A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398902 | ||||||
| chr6:170398923
|
C | CCCTTAGG others(340): Show |
2 | a0001c0008t0001g0098a0001c0008t0001g0099 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2692+3359_2692+336 others(351): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170398923 | |||||
| chr6:170398924
|
C | T | 54 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(51): Show | 59 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.2692+3345C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398924 | ||||||
| chr6:170398930
|
G | T | 1 | a0001c0002t0004g0025 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2692+3351G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398930 | ||||||
| chr6:170398939
|
A | G | 52 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(49): Show | 57 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.2692+3360A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398939 | ||||||
| chr6:170398941
|
A | G | 32 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(29): Show | 37 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.2692+3362A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398941 | ||||||
| chr6:170398954
|
T | C | 2 | a0005c0007t0012g0003a0005c0007t0028g0003 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2692+3375T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398954 | ||||||
| chr6:170398956
|
T | C | 1 | a0001c0002t0001g0082 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2692+3377T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398956 | ||||||
| chr6:170398962
|
C | G | 2 | a0005c0007t0012g0003a0005c0007t0028g0003 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2692+3383C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398962 | ||||||
| chr6:170398963
|
T | C | 2 | a0005c0007t0012g0003a0005c0007t0028g0003 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2692+3384T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398963 | ||||||
| chr6:170398969
|
G | A | 31 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(28): Show | 36 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.2692+3390G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398969 | ||||||
| chr6:170398973
|
G | T | 2 | a0001c0002t0001g0013a0001c0002t0001g0102 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2692+3394G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398973 | ||||||
| chr6:170398978
|
G | A | 1 | a0001c0002t0004g0025 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2692+3399G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398978 | ||||||
| chr6:170398980
|
A | G | 22 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(19): Show | 22 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2692+3401A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170398980 | ||||||
| chr6:170399000
|
ACT | A | 31 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(28): Show | 36 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.2692+3424_2692+342 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399000 | |||||
| chr6:170399002
|
T | C | 1 | a0001c0002t0004g0025 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2692+3423T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399002 | ||||||
| chr6:170399019
|
A | AAAGGTAG others(656): Show |
1 | a0001c0001t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2692+3515_2692+351 others(667): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399019 | |||||
| chr6:170399019
|
A | G | 23 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(20): Show | 23 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.2692+3440A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399019 | ||||||
| chr6:170399041
|
T | C | 31 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(28): Show | 36 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.2692+3462T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399041 | ||||||
| chr6:170399047
|
G | A | 2 | a0005c0007t0012g0003a0005c0007t0028g0003 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2692+3468G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399047 | ||||||
| chr6:170399047
|
G | GAGTGAGT others(2128): Show |
1 | a0001c0001t0006g0203 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2692+3655_2692+365 others(2139): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399047 | |||||
| chr6:170399056
|
G | A | 52 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(49): Show | 57 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.2692+3477G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399056 | ||||||
| chr6:170399058
|
G | A | 54 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(51): Show | 59 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.2692+3479G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399058 | ||||||
| chr6:170399078
|
ACT | A | 22 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(19): Show | 22 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2692+3502_2692+350 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399078 | |||||
| chr6:170399080
|
T | TCTTAGGA others(147): Show |
1 | a0001c0002t0001g0070 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2692+3515_2692+351 others(158): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399080 | |||||
| chr6:170399095
|
G | A | 48 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0014others(45): Show | 49 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(46): Show |
intron_variant | MODIFIER | c.2692+3516G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399095 | ||||||
| chr6:170399097
|
G | A | 81 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(78): Show | 87 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(84): Show |
intron_variant | MODIFIER | c.2692+3518G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399097 | ||||||
| chr6:170399119
|
T | C | 2 | a0005c0007t0012g0003a0005c0007t0028g0003 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2692+3540T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399119 | ||||||
| chr6:170399125
|
G | A | 21 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0001g0070others(18): Show | 21 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.2692+3546G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399125 | ||||||
| chr6:170399134
|
A | G | 52 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(49): Show | 57 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.2692+3555A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399134 | ||||||
| chr6:170399156
|
A | ACT | 53 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(50): Show | 58 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.2692+3578_2692+357 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399156 | |||||
| chr6:170399164
|
G | C | 1 | a0001c0002t0001g0102 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2692+3585G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399164 | ||||||
| chr6:170399171
|
G | A | 51 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(48): Show | 56 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.2692+3592G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399171 | ||||||
| chr6:170399173
|
G | A | 54 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(51): Show | 59 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.2692+3594G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399173 | ||||||
| chr6:170399195
|
T | C | 32 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(29): Show | 37 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.2692+3616T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399195 | ||||||
| chr6:170399201
|
A | G | 35 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(32): Show | 40 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.2692+3622A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399201 | ||||||
| chr6:170399201
|
A | T | 20 | a0001c0002t0001g0024a0001c0002t0001g0035a0001c0002t0004g0022others(17): Show | 20 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.2692+3622A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399201 | ||||||
| chr6:170399210
|
G | A | 32 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(29): Show | 37 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.2692+3631G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399210 | ||||||
| chr6:170399210
|
G | GGAAAGGT others(69): Show |
47 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0014others(44): Show | 48 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(45): Show |
intron_variant | MODIFIER | c.2692+3655_2692+365 others(80): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399210 | |||||
| chr6:170399210
|
G | GGAAAGGT others(418): Show |
1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2692+3655_2692+365 others(429): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399210 | |||||
| chr6:170399212
|
A | G | 52 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(49): Show | 57 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.2692+3633A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399212 | ||||||
| chr6:170399232
|
ACTCTTAG others(34): Show |
A | 1 | a0001c0002t0004g0025 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2692+3656_2692+369 others(45): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399232 | |||||
| chr6:170399234
|
T | TTAGGAGT others(30): Show |
9 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0041others(6): Show | 9 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2692+3655_2692+365 others(41): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399234 | ||||||
| chr6:170399249
|
A | G | 2 | a0001c0002t0001g0071a0001c0002t0001g0105 | 2 | HG00639.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2692+3670A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399249 | ||||||
| chr6:170399271
|
ACT | A | 9 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0041others(6): Show | 9 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2692+3695_2692+369 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399271 | |||||
| chr6:170399273
|
T | C | 54 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(51): Show | 59 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.2692+3694T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399273 | ||||||
| chr6:170399279
|
T | G | 67 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(64): Show | 73 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.2692+3700T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399279 | ||||||
| chr6:170399288
|
G | A | 3 | a0001c0002t0001g0071a0005c0007t0012g0003a0005c0007t0028g0003 | 3 | HG02451.hp1 HG03579.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2692+3709G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399288 | ||||||
| chr6:170399289
|
G | A | 1 | a0001c0002t0029g0091 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2692+3710G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399289 | ||||||
| chr6:170399290
|
G | A | 4 | a0001c0002t0001g0071a0001c0002t0001g0105a0001c0002t0004g0025others(1): Show | 5 | HG00639.hp1 HG02055.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.2692+3711G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399290 | ||||||
| chr6:170399318
|
G | A | 9 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0041others(6): Show | 9 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2692+3739G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399318 | ||||||
| chr6:170399322
|
G | C | 1 | a0001c0001t0006g0216 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2692+3743G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399322 | ||||||
| chr6:170399327
|
A | G | 53 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0014others(50): Show | 54 | HG00558.hp1 HG00639.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.2692+3748A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399327 | ||||||
| chr6:170399327
|
A | GGAAAGGT others(69): Show |
5 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0044others(2): Show | 5 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2692+3747_2692+374 others(80): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399327 | ||||||
| chr6:170399329
|
A | AAAGGTAG others(496): Show |
1 | a0001c0002t0001g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2692+3771_2692+377 others(507): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399329 | |||||
| chr6:170399329
|
A | G | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2692+3750A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399329 | ||||||
| chr6:170399339
|
C | CTATGTCA others(69): Show |
3 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0001g0043 | 3 | HG02965.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2692+3771_2692+377 others(80): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399339 | |||||
| chr6:170399351
|
C | T | 110 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(107): Show | 116 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.2692+3772C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399351 | ||||||
| chr6:170399354
|
T | C | 2 | a0001c0002t0001g0024a0001c0002t0001g0035 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2692+3775T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399354 | ||||||
| chr6:170399357
|
G | GAGTGAGT others(71): Show |
21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2692+3786_2692+378 others(82): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399357 | |||||
| chr6:170399357
|
G | T | 1 | a0001c0002t0001g0071 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2692+3778G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399357 | ||||||
| chr6:170399366
|
G | A | 2 | a0001c0002t0010g0103a0004c0005t0009g0090 | 2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2692+3787G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399366 | ||||||
| chr6:170399368
|
G | A | 51 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0014others(48): Show | 53 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(50): Show |
intron_variant | MODIFIER | c.2692+3789G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399368 | ||||||
| chr6:170399368
|
G | GAAGGTAG others(342): Show |
1 | a0001c0001t0006g0220 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2692+3826_2692+382 others(353): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399368 | |||||
| chr6:170399368
|
G | GAAGGTAG others(342): Show |
59 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0227others(56): Show | 59 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.2692+3927_2692+392 others(353): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399368 | |||||
| chr6:170399368
|
G | GAAGGTAG others(342): Show |
1 | a0001c0001t0005g0205 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2692+3927_2692+392 others(353): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399368 | |||||
| chr6:170399368
|
G | GAAGGTAG others(225): Show |
7 | a0001c0008t0001g0098a0001c0008t0001g0099a0004c0005t0001g0085others(4): Show | 7 | HG02886.hp1 HG02965.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2692+3927_2692+392 others(236): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399368 | |||||
| chr6:170399390
|
T | TCTTAGGA others(32): Show |
1 | a0001c0001t0010g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2692+3849_2692+385 others(43): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399390 | |||||
| chr6:170399396
|
G | A | 8 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0041others(5): Show | 8 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.2692+3817G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399396 | ||||||
| chr6:170399402
|
G | C | 2 | a0001c0002t0004g0028a0001c0002t0004g0029 | 2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.2692+3823G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399402 | ||||||
| chr6:170399405
|
A | G | 58 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0014others(55): Show | 59 | HG00558.hp1 HG00673.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.2692+3826A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399405 | ||||||
| chr6:170399407
|
A | G | 49 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0014others(46): Show | 50 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(47): Show |
intron_variant | MODIFIER | c.2692+3828A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399407 | ||||||
| chr6:170399429
|
T | C | 71 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(68): Show | 77 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.2692+3850T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399429 | ||||||
| chr6:170399429
|
T | TCTTAGGA others(225): Show |
4 | a0001c0002t0001g0013a0001c0002t0001g0102a0001c0009t0017g0093others(1): Show | 4 | HG02559.hp1 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2692+3927_2692+392 others(236): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399429 | |||||
| chr6:170399446
|
G | A | 1 | a0001c0002t0001g0071 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2692+3867G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399446 | ||||||
| chr6:170399446
|
G | GAAGGTAG others(108): Show |
6 | a0001c0002t0001g0001a0001c0002t0001g0048a0001c0002t0001g0056others(3): Show | 6 | HG00673.hp1 HG02129.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.2692+3928_2692+392 others(119): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399446 | |||||
| chr6:170399467
|
C | G | 1 | a0001c0002t0001g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2692+3888C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399467 | ||||||
| chr6:170399468
|
T | C | 9 | a0001c0002t0001g0021a0001c0002t0001g0031a0001c0002t0001g0041others(6): Show | 9 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2692+3889T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399468 | ||||||
| chr6:170399468
|
T | TCTTAGGA others(2711): Show |
1 | a0004c0005t0001g0084 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2692+3927_2692+392 others(2722): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399468 | |||||
| chr6:170399474
|
G | A | 3 | a0001c0002t0001g0105a0001c0002t0004g0025a0005c0007t0012g0002 | 4 | HG00639.hp1 HG02055.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.2692+3895G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399474 | ||||||
| chr6:170399480
|
G | GTGAGAAA others(342): Show |
1 | a0001c0001t0005g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2692+3927_2692+392 others(353): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399480 | |||||
| chr6:170399483
|
A | AGAAAGGT others(1935): Show |
4 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG02572.hp2 HG03130.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2692+3927_2692+392 others(1946): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399483 | |||||
| chr6:170399483
|
A | AGAAAGGT others(9859): Show |
1 | a0001c0006t0001g0255 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2692+3927_2692+392 others(9870): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399483 | |||||
| chr6:170399483
|
A | AGAAAGGT others(3682): Show |
1 | a0001c0001t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2692+3927_2692+392 others(3693): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399483 | |||||
| chr6:170399483
|
A | AGAAAGGT others(303): Show |
2 | a0001c0002t0013g0039a0001c0002t0013g0040 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2692+3927_2692+392 others(314): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399483 | |||||
| chr6:170399483
|
A | AGAAAGGT others(303): Show |
11 | a0001c0001t0001g0011a0001c0001t0001g0234a0001c0001t0001g0239others(8): Show | 12 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2692+3927_2692+392 others(314): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399483 | |||||
| chr6:170399483
|
A | AGAAAGGT others(1352): Show |
1 | a0001c0001t0005g0258 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2692+3927_2692+392 others(1363): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399483 | |||||
| chr6:170399483
|
A | AGAAAGGT others(303): Show |
1 | a0001c0001t0005g0217 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2692+3927_2692+392 others(314): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399483 | |||||
| chr6:170399483
|
A | AGAAAGGT others(303): Show |
2 | a0001c0001t0001g0260a0001c0006t0001g0246 | 2 | HG01167.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.2692+3927_2692+392 others(314): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399483 | |||||
| chr6:170399483
|
A | G | 55 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(52): Show | 61 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.2692+3904A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399483 | ||||||
| chr6:170399485
|
A | AAAGGTAG others(147): Show |
1 | a0001c0002t0001g0097 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2692+3919_2692+392 others(158): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399485 | |||||
| chr6:170399485
|
A | AAAGGTAG others(147): Show |
40 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0014others(37): Show | 40 | HG00558.hp1 HG01981.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.2692+3928_2692+392 others(158): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399485 | |||||
| chr6:170399485
|
A | G | 51 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(48): Show | 56 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.2692+3906A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399485 | ||||||
| chr6:170399505
|
ACT | A | 52 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(49): Show | 57 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.2692+3929_2692+393 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399505 | |||||
| chr6:170399507
|
T | C | 4 | a0001c0001t0006g0203a0001c0002t0029g0091a0005c0007t0012g0003others(1): Show | 4 | HG02451.hp1 HG03139.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.2692+3928T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399507 | ||||||
| chr6:170399513
|
G | T | 7 | a0001c0002t0001g0001a0001c0002t0001g0048a0001c0002t0001g0056others(4): Show | 7 | HG00673.hp1 HG02129.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.2692+3934G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399513 | ||||||
| chr6:170399522
|
G | A | 42 | a0001c0001t0010g0083a0001c0002t0001g0001a0001c0002t0001g0012others(39): Show | 42 | HG00558.hp1 HG01981.hp1 HG02015.hp2 others(39): Show |
intron_variant | MODIFIER | c.2692+3943G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399522 | ||||||
| chr6:170399524
|
G | A | 93 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(90): Show | 98 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.2692+3945G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399524 | ||||||
| chr6:170399524
|
G | GAAGGTAG others(108): Show |
3 | a0001c0002t0029g0091a0005c0007t0012g0003a0005c0007t0028g0003 | 3 | HG02451.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2692+3966_2692+396 others(119): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399524 | |||||
| chr6:170399546
|
C | T | 81 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(78): Show | 87 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.2692+3967C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399546 | ||||||
| chr6:170399552
|
G | A | 1 | a0001c0002t0001g0060 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2692+3973G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399552 | ||||||
| chr6:170399561
|
A | G | 47 | a0001c0001t0010g0083a0001c0002t0001g0001a0001c0002t0001g0012others(44): Show | 47 | HG00558.hp1 HG01981.hp1 HG02015.hp2 others(44): Show |
intron_variant | MODIFIER | c.2692+3982A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399561 | ||||||
| chr6:170399563
|
A | AAAGGTAG others(225): Show |
1 | a0001c0002t0001g0071 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2692+4005_2692+400 others(236): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399563 | |||||
| chr6:170399563
|
A | G | 42 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0014others(39): Show | 42 | HG00558.hp1 HG01981.hp1 HG02015.hp2 others(39): Show |
intron_variant | MODIFIER | c.2692+3984A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399563 | ||||||
| chr6:170399570
|
G | T | 23 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(20): Show | 27 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.2692+3991G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399570 | ||||||
| chr6:170399585
|
C | T | 69 | a0001c0001t0010g0083a0001c0002t0001g0001a0001c0002t0001g0012others(66): Show | 69 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.2692+4006C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399585 | ||||||
| chr6:170399600
|
A | G | 79 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(76): Show | 85 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2692+4021A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399600 | ||||||
| chr6:170399602
|
G | A | 79 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(76): Show | 84 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.2692+4023G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399602 | ||||||
| chr6:170399606
|
G | T | 1 | a0001c0001t0005g0221 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2692+4027G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399606 | ||||||
| chr6:170399623
|
G | C | 125 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(122): Show | 132 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.2692+4044G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399623 | ||||||
| chr6:170399624
|
C | T | 125 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(122): Show | 132 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.2692+4045C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399624 | ||||||
| chr6:170399639
|
G | A | 56 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(53): Show | 61 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.2692+4060G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399639 | ||||||
| chr6:170399641
|
G | A | 57 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(54): Show | 62 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.2692+4062G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399641 | ||||||
| chr6:170399661
|
A | ACT | 104 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(101): Show | 110 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.2692+4083_2692+408 others(6): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399661 | |||||
| chr6:170399667
|
G | A | 4 | a0001c0001t0010g0083a0001c0002t0029g0091a0005c0007t0012g0003others(1): Show | 4 | HG02451.hp1 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2692+4088G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399667 | ||||||
| chr6:170399676
|
G | A | 43 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0014others(40): Show | 43 | HG00558.hp1 HG01981.hp1 HG02015.hp2 others(40): Show |
intron_variant | MODIFIER | c.2692+4097G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399676 | ||||||
| chr6:170399678
|
G | A | 68 | a0001c0001t0010g0083a0001c0002t0001g0001a0001c0002t0001g0012others(65): Show | 69 | HG00558.hp1 HG00735.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.2692+4099G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399678 | ||||||
| chr6:170399682
|
G | A | 2 | a0005c0007t0012g0003a0005c0007t0028g0003 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2692+4103G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399682 | ||||||
| chr6:170399706
|
A | G | 74 | a0001c0001t0010g0083a0001c0002t0001g0001a0001c0002t0001g0012others(71): Show | 76 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.2692+4127A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399706 | ||||||
| chr6:170399715
|
G | A | 28 | a0001c0002t0001g0001a0001c0002t0001g0048a0001c0002t0001g0056others(25): Show | 29 | HG00673.hp1 HG00735.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.2692+4136G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399715 | ||||||
| chr6:170399717
|
A | G | 47 | a0001c0001t0010g0083a0001c0002t0001g0001a0001c0002t0001g0012others(44): Show | 47 | HG00558.hp1 HG01981.hp1 HG02015.hp2 others(44): Show |
intron_variant | MODIFIER | c.2692+4138A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399717 | ||||||
| chr6:170399739
|
T | C | 47 | a0001c0001t0010g0083a0001c0002t0001g0001a0001c0002t0001g0012others(44): Show | 47 | HG00558.hp1 HG01981.hp1 HG02015.hp2 others(44): Show |
intron_variant | MODIFIER | c.2692+4160T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399739 | ||||||
| chr6:170399739
|
T | TCTTAGGA others(617): Show |
1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2692+4176_2692+417 others(628): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399739 | |||||
| chr6:170399739
|
T | TCTTAGGA others(32): Show |
56 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(53): Show | 61 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.2692+4174_2692+417 others(43): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399739 | |||||
| chr6:170399739
|
T | TCTTAGGA others(188): Show |
21 | a0003c0004t0003g0005a0003c0004t0003g0152a0003c0004t0003g0153others(18): Show | 22 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2692+4174_2692+417 others(199): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399739 | |||||
| chr6:170399739
|
T | TTAGGAGT others(381): Show |
1 | a0011c0011t0001g0129 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2692+4160_2692+416 others(392): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399739 | ||||||
| chr6:170399756
|
G | A | 125 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(122): Show | 132 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.2692+4177G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399756 | ||||||
| chr6:170399756
|
G | GAAGGTAG others(6478): Show |
1 | a0001c0001t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2692+4220_2692+422 others(6489): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(2945): Show |
1 | a0001c0001t0005g0214 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(2956): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(1272): Show |
2 | a0001c0001t0001g0261a0001c0001t0005g0263 | 2 | HG00323.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.2692+4236_2692+423 others(1283): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3140): Show |
1 | a0001c0001t0001g0277 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(3151): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(966): Show |
1 | a0001c0001t0001g0204 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(977): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(1432): Show |
1 | a0001c0001t0001g0228 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(1443): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(1198): Show |
1 | a0001c0001t0005g0205 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(1209): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3140): Show |
2 | a0001c0002t0013g0039a0001c0002t0013g0040 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2692+4236_2692+423 others(3151): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(966): Show |
1 | a0001c0001t0001g0248 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(977): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3529): Show |
1 | a0001c0001t0001g0242 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(3540): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3179): Show |
2 | a0001c0008t0001g0098a0001c0008t0001g0099 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2692+4236_2692+423 others(3190): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3140): Show |
1 | a0001c0002t0001g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(3151): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3179): Show |
2 | a0001c0002t0001g0013a0001c0002t0001g0102 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2692+4236_2692+423 others(3190): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3526): Show |
1 | a0001c0001t0001g0234 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(3537): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3140): Show |
1 | a0001c0001t0001g0239 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(3151): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3140): Show |
6 | a0001c0001t0001g0011a0001c0001t0001g0272a0001c0001t0001g0273others(3): Show | 7 | HG00323.hp2 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2692+4236_2692+423 others(3151): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3140): Show |
1 | a0001c0002t0001g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(3151): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3101): Show |
3 | a0001c0001t0001g0260a0001c0006t0001g0246a0001c0006t0001g0255 | 3 | HG01167.hp2 NA18949.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2692+4236_2692+423 others(3112): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3179): Show |
2 | a0001c0009t0017g0093a0001c0009t0018g0092 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2692+4236_2692+423 others(3190): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(2011): Show |
1 | a0001c0001t0001g0230 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(2022): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3140): Show |
1 | a0001c0001t0005g0258 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(3151): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(2711): Show |
1 | a0001c0001t0001g0276 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(2722): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3140): Show |
4 | a0004c0005t0001g0085a0004c0005t0001g0086a0004c0005t0001g0087others(1): Show | 4 | HG02965.hp2 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2692+4236_2692+423 others(3151): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(4575): Show |
1 | a0004c0005t0001g0088 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(4586): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3140): Show |
1 | a0004c0005t0001g0084 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(3151): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(10091): Show |
1 | a0010c0013t0001g0237 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(10102): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(18561): Show |
1 | a0001c0001t0001g0229 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(18572): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(966): Show |
15 | a0001c0001t0001g0245a0001c0001t0001g0250a0001c0001t0001g0251others(12): Show | 15 | HG00738.hp1 HG00741.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2692+4236_2692+423 others(977): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(966): Show |
1 | a0001c0001t0001g0265 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(977): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(6441): Show |
1 | a0001c0001t0006g0203 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(6452): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3101): Show |
1 | a0001c0001t0005g0217 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(3112): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3606): Show |
7 | a0001c0002t0001g0031a0001c0002t0001g0041a0001c0002t0001g0042others(4): Show | 7 | HG01069.hp2 HG02145.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2692+4236_2692+423 others(3617): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(3606): Show |
1 | a0001c0002t0001g0021 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(3617): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(2945): Show |
1 | a0001c0018t0006g0215 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2692+4213_2692+421 others(2956): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399756
|
G | GAAGGTAG others(576): Show |
1 | a0001c0001t0001g0227 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2692+4213_2692+421 others(587): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399756 | |||||
| chr6:170399793
|
A | AGGAAGGT others(305): Show |
1 | a0001c0001t0006g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2692+4236_2692+423 others(316): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399793 | |||||
| chr6:170399816
|
G | C | 39 | a0001c0001t0001g0207a0001c0001t0001g0231a0001c0001t0001g0232others(36): Show | 40 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.2692+4237G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399816 | ||||||
| chr6:170399824
|
AGTGAGTG others(148): Show |
A | 1 | a0001c0002t0001g0094 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2692+4246_2692+440 others(4): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399824 | ||||||
| chr6:170399832
|
GGGAAGGT others(147): Show |
G | 2 | a0001c0002t0004g0025a0005c0007t0012g0002 | 3 | HG02055.hp1 HG03017.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2692+4278_2692+443 others(4): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399832 | |||||
| chr6:170399851
|
A | T | 1 | a0001c0001t0006g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2692+4272A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399851 | ||||||
| chr6:170399854
|
A | ACTCTTAG others(190): Show |
5 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0005g0208others(2): Show | 5 | HG00735.hp2 HG01496.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2692+4277_2692+427 others(201): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399854 | |||||
| chr6:170399854
|
A | ACTCTTAG others(268): Show |
24 | a0001c0001t0001g0207a0001c0001t0001g0231a0001c0001t0001g0232others(21): Show | 24 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.2692+4277_2692+427 others(279): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399854 | |||||
| chr6:170399854
|
A | ACTCTTAG others(734): Show |
1 | a0001c0001t0014g0226 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2692+4277_2692+427 others(745): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399854 | |||||
| chr6:170399854
|
A | ACTCTTAG others(656): Show |
1 | a0001c0001t0025g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2692+4277_2692+427 others(667): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399854 | |||||
| chr6:170399854
|
A | ACTCTTAG others(773): Show |
2 | a0001c0001t0005g0224a0001c0001t0006g0216 | 2 | HG02004.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2692+4277_2692+427 others(784): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399854 | |||||
| chr6:170399854
|
A | ACTCTTAG others(12852): Show |
1 | a0001c0001t0005g0221 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2692+4277_2692+427 others(12863): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399854 | |||||
| chr6:170399854
|
A | ACTCTTAG others(773): Show |
1 | a0001c0001t0020g0206 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2692+4277_2692+427 others(784): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399854 | |||||
| chr6:170399871
|
G | A | 3 | a0001c0001t0006g0222a0001c0001t0025g0187a0001c0002t0004g0027 | 3 | HG02109.hp1 HG03209.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.2692+4292G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399871 | ||||||
| chr6:170399888
|
A | T | 24 | a0001c0001t0001g0207a0001c0001t0001g0231a0001c0001t0001g0232others(21): Show | 24 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.2692+4309A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399888 | ||||||
| chr6:170399899
|
A | G | 35 | a0001c0001t0001g0207a0001c0001t0001g0231a0001c0001t0001g0232others(32): Show | 35 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.2692+4320A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399899 | ||||||
| chr6:170399908
|
G | A | 4 | a0001c0001t0005g0224a0001c0001t0006g0216a0001c0001t0014g0226others(1): Show | 4 | HG01934.hp2 HG02004.hp1 NA20905.hp2 others(1): Show |
intron_variant | MODIFIER | c.2692+4329G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399908 | ||||||
| chr6:170399910
|
A | G | 6 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0005g0208others(3): Show | 6 | HG00735.hp2 HG01496.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.2692+4331A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399910 | ||||||
| chr6:170399931
|
C | G | 5 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0005g0208others(2): Show | 5 | HG00735.hp2 HG01496.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2692+4352C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399931 | ||||||
| chr6:170399932
|
T | C | 6 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0265others(3): Show | 6 | HG00735.hp2 HG01496.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.2692+4353T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399932 | ||||||
| chr6:170399932
|
T | TCTTAGGA others(71): Show |
2 | a0001c0002t0013g0039a0001c0002t0013g0040 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2692+4367_2692+436 others(82): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399932 | |||||
| chr6:170399932
|
T | TTAGGAGT others(6010): Show |
1 | a0001c0001t0001g0240 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2692+4353_2692+435 others(6021): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399932 | ||||||
| chr6:170399947
|
G | A | 194 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0227others(191): Show | 202 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.2692+4368G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399947 | ||||||
| chr6:170399966
|
A | T | 5 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0005g0208others(2): Show | 5 | HG00735.hp2 HG01496.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2692+4387A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399966 | ||||||
| chr6:170399971
|
T | C | 195 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0227others(192): Show | 203 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.2692+4392T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399971 | ||||||
| chr6:170399971
|
T | TCTTAGGA others(11333): Show |
1 | a0001c0001t0001g0243 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(11344): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(11216): Show |
1 | a0001c0001t0005g0225 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(11227): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(15063): Show |
1 | a0001c0001t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(15074): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(11255): Show |
1 | a0001c0001t0006g0172 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(11266): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(11294): Show |
1 | a0001c0001t0005g0208 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(11305): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(16645): Show |
1 | a0001c0001t0001g0235 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(16656): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(16615): Show |
1 | a0001c0001t0001g0236 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(16626): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(16693): Show |
1 | a0001c0001t0001g0238 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(16704): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(10442): Show |
1 | a0001c0001t0001g0232 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(10453): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(16612): Show |
1 | a0001c0001t0001g0231 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(16623): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(16692): Show |
1 | a0001c0001t0001g0233 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(16703): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(7876): Show |
1 | a0001c0001t0005g0218 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(7887): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(11216): Show |
1 | a0001c0001t0005g0202 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(11227): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(11216): Show |
1 | a0001c0001t0005g0249 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(11227): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(11216): Show |
4 | a0001c0001t0005g0171a0001c0001t0006g0173a0001c0001t0006g0175others(1): Show | 4 | HG01175.hp1 HG01361.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.2692+4406_2692+440 others(11227): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(7876): Show |
1 | a0001c0001t0026g0223 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(7887): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(7876): Show |
1 | a0001c0001t0005g0219 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(7887): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(7837): Show |
1 | a0001c0001t0001g0207 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(7848): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(11216): Show |
1 | a0001c0001t0006g0220 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(11227): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(11682): Show |
1 | a0001c0001t0005g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(11693): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399971
|
T | TCTTAGGA others(11216): Show |
1 | a0001c0001t0006g0176 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(11227): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399971 | |||||
| chr6:170399985
|
G | GGGGAAGG others(11216): Show |
1 | a0001c0001t0006g0209 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(11227): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399985 | ||||||
| chr6:170399985
|
G | GGGGAAGG others(11216): Show |
1 | a0001c0001t0027g0210 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(11227): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399985 | ||||||
| chr6:170399985
|
G | GGGGAAGG others(11021): Show |
1 | a0001c0001t0006g0256 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(11032): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399985 | ||||||
| chr6:170399985
|
G | GGGGAAGG others(11177): Show |
1 | a0001c0001t0006g0174 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2692+4406_2692+440 others(11188): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399985 | ||||||
| chr6:170399986
|
A | AGAAAGGT others(12655): Show |
1 | a0001c0001t0006g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2692+4408_2692+440 others(12666): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGAAAGGT others(264): Show |
1 | a0001c0001t0005g0221 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2692+4408_2692+440 others(275): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(344): Show |
1 | a0001c0001t0025g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2692+4430_2692+443 others(355): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(32): Show |
114 | a0001c0001t0001g0011a0001c0001t0001g0229a0001c0001t0001g0230others(111): Show | 121 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.2692+4430_2692+443 others(43): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(12616): Show |
1 | a0001c0001t0001g0265 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2692+4430_2692+443 others(12627): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(12267): Show |
2 | a0001c0006t0001g0253a0001c0006t0001g0254 | 2 | NA18968.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2692+4430_2692+443 others(12278): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(15022): Show |
1 | a0001c0001t0001g0264 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2692+4430_2692+443 others(15033): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(12618): Show |
1 | a0001c0001t0001g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2692+4430_2692+443 others(12629): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(12616): Show |
1 | a0001c0001t0001g0248 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2692+4430_2692+443 others(12627): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(12614): Show |
2 | a0001c0001t0001g0266a0001c0001t0001g0270 | 2 | HG00738.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.2692+4430_2692+443 others(12625): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(12616): Show |
3 | a0001c0001t0001g0204a0001c0001t0001g0245a0001c0001t0001g0259 | 3 | HG02738.hp2 HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2692+4430_2692+443 others(12627): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(12618): Show |
1 | a0001c0015t0001g0252 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2692+4430_2692+443 others(12629): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(9237): Show |
1 | a0001c0001t0001g0269 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2692+4430_2692+443 others(9248): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(12614): Show |
1 | a0001c0001t0001g0267 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2692+4430_2692+443 others(12625): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(17428): Show |
1 | a0001c0001t0001g0251 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2692+4430_2692+443 others(17439): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(12616): Show |
1 | a0001c0001t0001g0262 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2692+4430_2692+443 others(12627): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(13820): Show |
1 | a0001c0001t0001g0228 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2692+4430_2692+443 others(13831): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(10052): Show |
1 | a0001c0001t0005g0205 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2692+4430_2692+443 others(10063): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(2984): Show |
1 | a0001c0001t0005g0214 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2692+4430_2692+443 others(2995): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(15683): Show |
1 | a0001c0001t0001g0250 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2692+4430_2692+443 others(15694): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(13782): Show |
1 | a0001c0001t0001g0261 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2692+4430_2692+443 others(13793): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(10366): Show |
1 | a0001c0001t0005g0263 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2692+4430_2692+443 others(10377): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | AGGAAGGT others(31): Show |
49 | a0001c0002t0001g0001a0001c0002t0001g0012a0001c0002t0001g0014others(46): Show | 50 | HG00558.hp1 HG00673.hp1 HG01981.hp1 others(47): Show |
intron_variant | MODIFIER | c.2692+4430_2692+443 others(42): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399986 | |||||
| chr6:170399986
|
A | G | 32 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(29): Show | 32 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.2692+4407A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399986 | ||||||
| chr6:170399988
|
G | A | 4 | a0001c0001t0005g0224a0001c0001t0006g0216a0001c0001t0014g0226others(1): Show | 4 | HG01934.hp2 HG02004.hp1 NA20905.hp2 others(1): Show |
intron_variant | MODIFIER | c.2692+4409G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170399988 | ||||||
| chr6:170399997
|
A | ACTATGTC others(32): Show |
5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(2): Show | 5 | HG02572.hp2 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2692+4430_2692+443 others(43): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399997 | |||||
| chr6:170399997
|
A | ACTATGTC others(9469): Show |
1 | a0001c0001t0001g0275 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2692+4445_2692+444 others(9480): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170399997 | |||||
| chr6:170400005
|
A | ATAACCCT others(344): Show |
1 | a0001c0001t0001g0227 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2692+4430_2692+443 others(355): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170400005 | |||||
| chr6:170400010
|
T | C | 7 | a0001c0001t0001g0207a0001c0001t0001g0234a0001c0001t0005g0224others(4): Show | 7 | HG00741.hp2 HG01934.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.2692+4431T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400010 | ||||||
| chr6:170400025
|
G | A | 4 | a0001c0001t0005g0224a0001c0001t0006g0216a0001c0001t0014g0226others(1): Show | 4 | HG01934.hp2 HG02004.hp1 NA20905.hp2 others(1): Show |
intron_variant | MODIFIER | c.2692+4446G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400025 | ||||||
| chr6:170400027
|
G | AAAGGTAG others(10711): Show |
1 | a0001c0001t0014g0226 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2692+4447_2692+444 others(10722): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400027 | ||||||
| chr6:170400027
|
G | AAAGGTAG others(10711): Show |
1 | a0001c0001t0020g0206 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2692+4447_2692+444 others(10722): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400027 | ||||||
| chr6:170400027
|
G | AAAGGTAG others(10711): Show |
1 | a0001c0001t0006g0216 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2692+4447_2692+444 others(10722): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400027 | ||||||
| chr6:170400027
|
G | AAAGGTAG others(10711): Show |
1 | a0001c0001t0005g0224 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2692+4447_2692+444 others(10722): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400027 | ||||||
| chr6:170400027
|
G | AAAGGTAG others(11372): Show |
1 | a0001c0001t0001g0227 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2692+4447_2692+444 others(11383): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400027 | ||||||
| chr6:170400057
|
G | GTGAGTGG others(9389): Show |
1 | a0001c0001t0025g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2693-4234_2693-423 others(9400): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170400057 | |||||
| chr6:170400063
|
G | GGGGAAGG others(31): Show |
1 | a0001c0001t0001g0234 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2693-4464_2693-446 others(42): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170400063 | |||||
| chr6:170400087
|
G | C | 1 | a0001c0001t0009g0278 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2693-4463G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400087 | ||||||
| chr6:170400087
|
G | GCCTTAGG others(12226): Show |
1 | a0001c0001t0001g0268 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2693-4234_2693-423 others(12237): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170400087 | |||||
| chr6:170400088
|
C | T | 1 | a0001c0001t0009g0278 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2693-4462C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400088 | ||||||
| chr6:170400103
|
A | G | 1 | a0001c0001t0009g0278 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2693-4447A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400103 | ||||||
| chr6:170400105
|
A | G | 1 | a0001c0001t0009g0278 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2693-4445A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400105 | ||||||
| chr6:170400126
|
C | G | 1 | a0001c0001t0009g0278 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2693-4424C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400126 | ||||||
| chr6:170400129
|
T | G | 1 | a0001c0001t0005g0258 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2693-4421T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400129 | ||||||
| chr6:170400142
|
G | A | 36 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(33): Show | 42 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2693-4408G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400142 | ||||||
| chr6:170400144
|
G | A | 1 | a0001c0001t0009g0278 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2693-4406G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400144 | ||||||
| chr6:170400149
|
T | C | 5 | a0001c0001t0009g0009a0001c0001t0009g0188a0001c0001t0009g0189others(2): Show | 6 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2693-4401T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400149 | ||||||
| chr6:170400205
|
C | CCTTAGGA others(32): Show |
1 | a0001c0001t0005g0221 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2693-4307_2693-426 others(43): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170400205 | |||||
| chr6:170400213
|
G | T | 1 | a0001c0001t0008g0192 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2693-4337G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400213 | ||||||
| chr6:170400300
|
G | A | 1 | a0001c0002t0013g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2693-4250G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400300 | ||||||
| chr6:170400311
|
T | G | 5 | a0001c0001t0010g0095a0001c0001t0010g0096a0005c0007t0012g0002others(2): Show | 6 | HG02055.hp1 HG02451.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2693-4239T>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400311 | ||||||
| chr6:170400402
|
C | T | 1 | a0001c0001t0025g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2693-4148C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400402 | ||||||
| chr6:170400460
|
C | T | 83 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(80): Show | 84 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.2693-4090C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400460 | ||||||
| chr6:170400731
|
A | G | 1 | a0001c0001t0010g0083 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2693-3819A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400731 | ||||||
| chr6:170400843
|
G | T | 1 | a0001c0001t0005g0221 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2693-3707G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400843 | ||||||
| chr6:170400937
|
C | G | 5 | a0001c0001t0010g0095a0001c0001t0010g0096a0005c0007t0012g0002others(2): Show | 6 | HG02055.hp1 HG02451.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2693-3613C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170400937 | ||||||
| chr6:170401081
|
G | A | 2 | a0003c0004t0015g0151a0003c0004t0015g0155 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2693-3469G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170401081 | ||||||
| chr6:170401082
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2693-3468C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170401082 | ||||||
| chr6:170401088
|
G | C | 3 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0242 | 3 | HG01243.hp1 HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2693-3462G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170401088 | ||||||
| chr6:170401097
|
T | C | 2 | a0001c0002t0010g0103a0004c0005t0009g0090 | 2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2693-3453T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170401097 | ||||||
| chr6:170401123
|
C | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0250 | 2 | HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2693-3427C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170401123 | ||||||
| chr6:170401304
|
G | A | 4 | a0001c0002t0001g0013a0001c0002t0001g0102a0001c0009t0017g0093others(1): Show | 4 | HG02559.hp1 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2693-3246G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170401304 | ||||||
| chr6:170401340
|
G | A | 24 | a0001c0001t0001g0204a0001c0001t0001g0245a0001c0001t0001g0247others(21): Show | 24 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.2693-3210G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170401340 | ||||||
| chr6:170401458
|
G | A | 3 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0001g0043 | 3 | HG02965.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2693-3092G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170401458 | ||||||
| chr6:170401542
|
C | T | 1 | a0001c0002t0001g0082 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2693-3008C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170401542 | ||||||
| chr6:170401543
|
G | A | 6 | a0004c0005t0001g0084a0004c0005t0001g0085a0004c0005t0001g0086others(3): Show | 6 | HG02965.hp2 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2693-3007G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170401543 | ||||||
| chr6:170401566
|
C | G | 23 | a0002c0003t0002g0106a0002c0003t0002g0108a0002c0003t0002g0114others(20): Show | 23 | HG00558.hp2 HG00673.hp2 HG02155.hp1 others(20): Show |
intron_variant | MODIFIER | c.2693-2984C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170401566 | ||||||
| chr6:170401603
|
A | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0240 | 2 | HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2693-2947A>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170401603 | ||||||
| chr6:170401945
|
AG | A | 109 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0207others(106): Show | 110 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.2693-2604delG | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170401945 | ||||||
| chr6:170402001
|
C | T | 2 | a0001c0002t0001g0054a0002c0003t0022g0144 | 2 | HG02004.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2693-2549C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170402001 | ||||||
| chr6:170402045
|
C | T | 1 | a0001c0001t0008g0200 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2693-2505C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170402045 | ||||||
| chr6:170402108
|
C | G | 1 | a0001c0001t0005g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2693-2442C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170402108 | ||||||
| chr6:170402348
|
T | A | 1 | a0002c0003t0002g0136 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2693-2202T>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170402348 | ||||||
| chr6:170402473
|
C | T | 1 | a0001c0001t0005g0258 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2693-2077C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170402473 | ||||||
| chr6:170402538
|
G | A | 1 | a0002c0003t0023g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2693-2012G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170402538 | ||||||
| chr6:170402638
|
C | T | 1 | a0001c0002t0010g0103 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2693-1912C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170402638 | ||||||
| chr6:170402740
|
T | C | 137 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0227others(134): Show | 141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.2693-1810T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170402740 | ||||||
| chr6:170402748
|
G | A | 2 | a0001c0008t0001g0098a0001c0008t0001g0099 | 2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2693-1802G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170402748 | ||||||
| chr6:170403091
|
C | T | 36 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(33): Show | 42 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.2693-1459C>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170403091 | ||||||
| chr6:170403168
|
A | G | 48 | a0001c0001t0001g0207a0001c0002t0001g0001a0001c0002t0001g0036others(45): Show | 49 | HG00558.hp1 HG00673.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.2693-1382A>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170403168 | ||||||
| chr6:170403432
|
TG | T | 38 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(35): Show | 44 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.2693-1117delG | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170403432 | ||||||
| chr6:170403530
|
G | A | 1 | a0001c0002t0004g0027 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2693-1020G>A | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170403530 | ||||||
| chr6:170403631
|
G | T | 1 | a0001c0001t0001g0262 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2693-919G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170403631 | ||||||
| chr6:170403681
|
G | T | 2 | a0001c0002t0013g0039a0001c0002t0013g0040 | 2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2693-869G>T | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170403681 | ||||||
| chr6:170404061
|
GA | G | 3 | a0001c0006t0001g0253a0001c0006t0001g0254a0001c0006t0001g0255 | 3 | NA18968.hp1 NA19085.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2693-484delA | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr6 | 170404061 | |||||
| chr6:170404311
|
G | C | 38 | a0001c0001t0008g0010a0001c0001t0008g0192a0001c0001t0008g0194others(35): Show | 44 | HG00280.hp1 HG00733.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.2693-239G>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170404311 | ||||||
| chr6:170404415
|
C | G | 48 | a0001c0001t0001g0207a0001c0002t0001g0001a0001c0002t0001g0036others(45): Show | 49 | HG00558.hp1 HG00673.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.2693-135C>G | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170404415 | ||||||
| chr6:170404534
|
T | C | 1 | a0001c0002t0001g0013 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2693-16T>C | FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 9/10 | chr6 | 170404534 |