Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23201 |
|---|---|
| ensemblid | ENSG00000054965.11 |
| hgncid | 28999 |
| symbol | FAM168A |
| name | family with sequence similarity 168 member A |
| refseq_nuc | NM_015159.3 |
| refseq_prot | NP_055974.1 |
| ensembl_nuc | ENST00000356467.5 |
| ensembl_prot | ENSP00000348852.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 73400487 |
| end | 73598112 |
| strand | - |
| ver | v1.2 |
| region | chr11:73400487-73598112 |
| region5000 | chr11:73395487-73603112 |
| regionname0 | FAM168A_chr11_73400487_73598112 |
| regionname5000 | FAM168A_chr11_73395487_73603112 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 235 | 179 | 86 | 25 | 44 | 10 | 12 | 34 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0002 | 0/0 | 235 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 708 | 90 | 55 | 9 | 16 | 4 | 6 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| c0002 | 1/1 | 708 | 85 | 28 | 16 | 27 | 6 | 6 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| c0003 | 0/0 | 708 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| c0004 | 0/0 | 708 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| c0005 | 0/0 | 708 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| c0006 | 0/0 | 708 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 6485 | 52 | 16 | 8 | 19 | 3 | 4 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0002 | 0/0 | 6484 | 15 | 15 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0003 | 0/0 | 6488 | 14 | 0 | 1 | 13 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0004 | 0/0 | 6491 | 11 | 11 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0005 | 0/0 | 6488 | 8 | 1 | 3 | 2 | 1 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0006 | 0/0 | 6481 | 6 | 4 | 0 | 0 | 1 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0007 | 0/0 | 6482 | 5 | 0 | 3 | 0 | 0 | 2 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0008 | 0/0 | 6488 | 4 | 0 | 2 | 0 | 2 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0009 | 0/0 | 6485 | 4 | 3 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0010 | 0/0 | 6487 | 3 | 1 | 0 | 2 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0011 | 0/0 | 6491 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0012 | 0/0 | 6485 | 3 | 0 | 0 | 3 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0013 | 0/0 | 6485 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0014 | 0/0 | 6485 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0015 | 0/0 | 6485 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0016 | 0/0 | 6491 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0017 | 0/0 | 6482 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0018 | 0/0 | 6494 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0019 | 0/0 | 6499 | 2 | 1 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0020 | 0/0 | 6488 | 2 | 0 | 2 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0021 | 0/0 | 6485 | 2 | 0 | 0 | 2 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0022 | 0/0 | 6491 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0023 | 0/0 | 6485 | 2 | 0 | 2 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0024 | 0/0 | 6487 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0025 | 0/0 | 6494 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0026 | 0/0 | 6482 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0027 | 0/0 | 6485 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0028 | 0/0 | 6487 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0029 | 0/0 | 6494 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0030 | 0/0 | 6488 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0031 | 0/0 | 6485 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0032 | 0/0 | 6485 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0033 | 0/0 | 6482 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0034 | 0/0 | 6488 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0035 | 0/0 | 6482 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0036 | 0/0 | 6488 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0037 | 0/0 | 6491 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0038 | 0/0 | 6488 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0039 | 0/0 | 6488 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0040 | 0/0 | 6491 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0041 | 0/0 | 6491 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0042 | 0/0 | 6490 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0043 | 0/0 | 6496 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0044 | 0/0 | 6485 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0045 | 0/0 | 6485 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0046 | 0/0 | 6485 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0047 | 0/0 | 6488 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0048 | 0/0 | 6484 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0049 | 0/0 | 6488 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0050 | 0/0 | 6485 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0051 | 0/0 | 6485 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| t0052 | 0/0 | 6488 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0031 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 708 | 90 | 55 | 9 | 16 | 4 | 6 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002 | 1/1 | 708 | 85 | 28 | 16 | 27 | 6 | 6 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0003 | 0/0 | 708 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0004 | 0/0 | 708 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0006 | 0/0 | 708 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0002c0005 | 0/0 | 708 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 7191 | 15 | 15 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0003 | 0/0 | 7195 | 14 | 0 | 1 | 13 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0004 | 0/0 | 7198 | 10 | 10 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0006 | 0/0 | 7188 | 6 | 4 | 0 | 0 | 1 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0007 | 0/0 | 7189 | 5 | 0 | 3 | 0 | 0 | 2 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0008 | 0/0 | 7195 | 4 | 0 | 2 | 0 | 2 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0010 | 0/0 | 7194 | 3 | 1 | 0 | 2 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0011 | 0/0 | 7198 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0014 | 0/0 | 7192 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0015 | 0/0 | 7192 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0016 | 0/0 | 7198 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0017 | 0/0 | 7189 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0018 | 0/0 | 7201 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0019 | 0/0 | 7206 | 2 | 1 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0022 | 0/0 | 7198 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0024 | 0/0 | 7194 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0025 | 0/0 | 7201 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0026 | 0/0 | 7189 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0027 | 0/0 | 7192 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0029 | 0/0 | 7201 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0030 | 0/0 | 7195 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0034 | 0/0 | 7195 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0035 | 0/0 | 7189 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0036 | 0/0 | 7195 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0037 | 0/0 | 7198 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0039 | 0/0 | 7195 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0040 | 0/0 | 7198 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0041 | 0/0 | 7198 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0042 | 0/0 | 7197 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0043 | 0/0 | 7203 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0001t0052 | 0/0 | 7195 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0001 | 1/1 | 7192 | 50 | 16 | 7 | 18 | 3 | 4 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0005 | 0/0 | 7195 | 8 | 1 | 3 | 2 | 1 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0009 | 0/0 | 7192 | 3 | 2 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0012 | 0/0 | 7192 | 3 | 0 | 0 | 3 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0013 | 0/0 | 7192 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0020 | 0/0 | 7195 | 2 | 0 | 2 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0021 | 0/0 | 7192 | 2 | 0 | 0 | 2 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0023 | 0/0 | 7192 | 2 | 0 | 2 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0031 | 0/0 | 7192 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0032 | 0/0 | 7192 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0033 | 0/0 | 7189 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0038 | 0/0 | 7195 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0044 | 0/0 | 7192 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0045 | 0/0 | 7192 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0046 | 0/0 | 7192 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0047 | 0/0 | 7195 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0048 | 0/0 | 7191 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0049 | 0/0 | 7195 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0050 | 0/0 | 7192 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0002t0051 | 0/0 | 7192 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0003t0004 | 0/0 | 7198 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0003t0028 | 0/0 | 7194 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0004t0009 | 0/0 | 7192 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0001c0006t0001 | 0/0 | 7192 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| a0002c0005t0001 | 0/0 | 7192 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | copy fasta | chr11 | 73395487 | 73603112 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0006g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0007g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0007g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0007g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0007g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0007g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0008g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0008g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0008g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0008g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0010g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0010g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0014g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0014g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0015g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0015g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0016g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0016g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0017g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0017g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0018g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0018g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0019g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0019g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0022g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0022g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0024g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0025g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0026g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0027g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0029g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0030g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0034g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0035g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0036g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0037g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0039g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0040g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0041g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0042g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0043g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0001t0052g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0031 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0005g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0009g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0009g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0012g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0012g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0012g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0013g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0013g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0013g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0020g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0020g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0021g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0021g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0023g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0023g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0031g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0032g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0033g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0038g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0044g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0045g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0046g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0047g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0048g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0049g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0050g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0002t0051g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0003t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0003t0028g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0004t0009g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0001c0006t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| a0002c0005t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0117 | EUR | GBR | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0024 | EUR | GBR | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG00323 | hp1 | a0001 | c0001 | t0035 | g0179 | EUR | FIN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG00323 | hp2 | a0001 | c0002 | t0051 | g0108 | EUR | FIN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | CHS | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | CHS | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | CHS | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | CHS | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01069 | hp1 | a0001 | c0002 | t0005 | g0085 | AMR | PUR | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PUR | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01106 | hp2 | a0001 | c0001 | t0019 | g0069 | AMR | PUR | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01109 | hp2 | a0002 | c0005 | t0001 | g0055 | AMR | PUR | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01167 | hp1 | a0001 | c0002 | t0020 | g0040 | AMR | PUR | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0023 | AMR | PUR | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01168 | hp1 | a0001 | c0002 | t0023 | g0107 | AMR | PUR | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01168 | hp2 | a0001 | c0001 | t0008 | g0159 | AMR | PUR | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01169 | hp1 | a0001 | c0002 | t0020 | g0109 | AMR | PUR | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01169 | hp2 | a0001 | c0002 | t0023 | g0051 | AMR | PUR | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | CLM | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0025 | AMR | CLM | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | CLM | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01257 | hp2 | a0001 | c0002 | t0009 | g0076 | AMR | CLM | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | CLM | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01261 | hp2 | a0001 | c0001 | t0008 | g0175 | AMR | CLM | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | CLM | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01433 | hp2 | a0001 | c0001 | t0037 | g0177 | AMR | CLM | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01515 | hp1 | a0001 | c0002 | t0048 | g0043 | EUR | IBS | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01515 | hp2 | a0001 | c0001 | t0008 | g0172 | EUR | IBS | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0038 | EUR | IBS | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01517 | hp2 | a0001 | c0001 | t0008 | g0173 | EUR | IBS | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0139 | AFR | ACB | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01884 | hp2 | a0001 | c0001 | t0019 | g0070 | AFR | ACB | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01928 | hp1 | a0001 | c0002 | t0005 | g0047 | AMR | PEL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01928 | hp2 | a0001 | c0001 | t0034 | g0174 | AMR | PEL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01934 | hp1 | a0001 | c0002 | t0005 | g0048 | AMR | PEL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01934 | hp2 | a0001 | c0001 | t0007 | g0022 | AMR | PEL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0162 | AMR | PEL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG01978 | hp2 | a0001 | c0002 | t0038 | g0041 | AMR | PEL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | KHV | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | KHV | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02040 | hp1 | a0001 | c0002 | t0045 | g0112 | EAS | KHV | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | KHV | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02055 | hp1 | a0001 | c0001 | t0017 | g0032 | AFR | ACB | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02055 | hp2 | a0001 | c0001 | t0039 | g0125 | AFR | ACB | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | KHV | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02083 | hp2 | a0001 | c0002 | t0021 | g0104 | EAS | KHV | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | ACB | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | ACB | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02258 | hp1 | a0001 | c0002 | t0013 | g0102 | AFR | ACB | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02258 | hp2 | a0001 | c0001 | t0015 | g0133 | AFR | ACB | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | ACB | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02572 | hp1 | a0001 | c0001 | t0018 | g0128 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02615 | hp1 | a0001 | c0001 | t0016 | g0136 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02615 | hp2 | a0001 | c0003 | t0028 | g0064 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02622 | hp2 | a0001 | c0001 | t0022 | g0062 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02630 | hp1 | a0001 | c0004 | t0009 | g0074 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02647 | hp1 | a0001 | c0002 | t0013 | g0101 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02647 | hp2 | a0001 | c0001 | t0040 | g0126 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02683 | hp1 | a0001 | c0001 | t0007 | g0026 | SAS | PJL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | PJL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0142 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02723 | hp1 | a0001 | c0002 | t0013 | g0103 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0121 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02818 | hp1 | a0001 | c0002 | t0005 | g0110 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02818 | hp2 | a0001 | c0001 | t0022 | g0061 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02895 | hp2 | a0001 | c0001 | t0011 | g0150 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02897 | hp2 | a0001 | c0001 | t0011 | g0149 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02922 | hp2 | a0001 | c0002 | t0009 | g0105 | AFR | ESN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | ESN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | ESN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02970 | hp1 | a0001 | c0001 | t0027 | g0146 | AFR | ESN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02970 | hp2 | a0001 | c0001 | t0029 | g0141 | AFR | ESN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | ESN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03041 | hp1 | a0001 | c0001 | t0026 | g0144 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0123 | AFR | MSL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0067 | AFR | MSL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | ESN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03130 | hp2 | a0001 | c0002 | t0033 | g0077 | AFR | ESN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03139 | hp1 | a0001 | c0001 | t0041 | g0134 | AFR | ESN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03195 | hp2 | a0001 | c0001 | t0015 | g0132 | AFR | ESN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0081 | AFR | MSL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0153 | AFR | MSL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03225 | hp1 | a0001 | c0001 | t0014 | g0154 | AFR | MSL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03225 | hp2 | a0001 | c0002 | t0049 | g0072 | AFR | MSL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03239 | hp1 | a0001 | c0001 | t0007 | g0027 | SAS | PJL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03453 | hp1 | a0001 | c0001 | t0043 | g0068 | AFR | MSL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03490 | hp1 | a0001 | c0001 | t0030 | g0156 | SAS | PJL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0089 | AFR | ESN | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0095 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | GWD | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | MSL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | MSL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03710 | hp1 | a0001 | c0001 | t0052 | g0157 | SAS | PJL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03710 | hp2 | a0001 | c0002 | t0050 | g0131 | SAS | PJL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03831 | hp1 | a0001 | c0001 | t0036 | g0178 | SAS | BEB | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0106 | SAS | BEB | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | YRI | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18522 | hp2 | a0001 | c0001 | t0011 | g0148 | AFR | YRI | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0135 | AFR | YRI | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18906 | hp2 | a0001 | c0002 | t0047 | g0114 | AFR | YRI | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18965 | hp1 | a0001 | c0001 | t0024 | g0003 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18968 | hp1 | a0001 | c0006 | t0001 | g0083 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18981 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18981 | hp2 | a0001 | c0002 | t0005 | g0059 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18984 | hp1 | a0001 | c0002 | t0031 | g0111 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA18984 | hp2 | a0001 | c0002 | t0012 | g0084 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19030 | hp1 | a0001 | c0002 | t0046 | g0100 | AFR | LWK | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19030 | hp2 | a0001 | c0001 | t0042 | g0060 | AFR | LWK | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | LWK | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19043 | hp2 | a0001 | c0001 | t0018 | g0130 | AFR | LWK | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19056 | hp1 | a0001 | c0002 | t0012 | g0082 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19060 | hp1 | a0001 | c0002 | t0005 | g0050 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19060 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19077 | hp2 | a0001 | c0002 | t0021 | g0054 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19083 | hp1 | a0001 | c0002 | t0012 | g0113 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | YRI | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA19240 | hp2 | a0001 | c0002 | t0009 | g0073 | AFR | YRI | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | ASW | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0140 | AFR | ASW | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA20805 | hp1 | a0001 | c0002 | t0005 | g0155 | EUR | TSI | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0037 | EUR | TSI | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA20905 | hp1 | a0001 | c0002 | t0005 | g0092 | SAS | GIH | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0180 | SAS | GIH | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02109 | hp1 | a0001 | c0002 | t0032 | g0116 | AFR | ACB | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02109 | hp2 | a0001 | c0003 | t0004 | g0063 | AFR | ACB | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02559 | hp1 | a0001 | c0002 | t0044 | g0049 | AFR | ACB | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG02559 | hp2 | a0001 | c0001 | t0017 | g0078 | AFR | ACB | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | MSL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA20300 | hp1 | a0001 | c0001 | t0025 | g0120 | AFR | USA | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | USA | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | LWK | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0004 | AFR | LWK | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0031 | REF | REF | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0030 | REF | REF | FAM168A_chr11_73395487_73603112 | FAM168A | chr11 | 73395487 | 73603112 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:73430743
|
G | A | 1 | a0002 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.98C>T | p.Ala33Val | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/8 | 306/7192 | 98/708 | 33/235 | chr11 | 73430743 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:73407558
|
C | T | 1 | a0001c0003 | 2 | HG02109.hp2 HG02615.hp2 |
synonymous_variant | LOW | c.681G>A | p.Ala227Ala | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 7/8 | 889/7192 | 681/708 | 227/235 | chr11 | 73407558 | ||
| chr11:73409608
|
A | G | 2 | a0001c0001a0001c0003 | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
synonymous_variant | LOW | c.474T>C | p.His158His | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 6/8 | 682/7192 | 474/708 | 158/235 | chr11 | 73409608 | ||
| chr11:73430718
|
G | A | 1 | a0001c0004 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.123C>T | p.Tyr41Tyr | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/8 | 331/7192 | 123/708 | 41/235 | chr11 | 73430718 | ||
| chr11:73468406
|
C | A | 1 | a0001c0006 | 1 | NA18968.hp1 | splice_region_variant&synonymous_variant | LOW | c.69G>T | p.Thr23Thr | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/8 | 277/7192 | 69/708 | 23/235 | chr11 | 73468406 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:73400513
|
G | A | 1 | a0001c0001t0024 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6250C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 7018 | chr11 | 73400513 | |||||
| chr11:73400572
|
T | G | 12 | a0001c0001t0003a0001c0001t0008a0001c0001t0016others(9): Show | 30 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*6191A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6959 | chr11 | 73400572 | |||||
| chr11:73400574
|
A | T | 1 | a0001c0002t0012 | 3 | NA18984.hp2 NA19056.hp1 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6189T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6957 | chr11 | 73400574 | |||||
| chr11:73400732
|
G | T | 1 | a0001c0001t0036 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6031C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6799 | chr11 | 73400732 | |||||
| chr11:73400808
|
AT | A | 4 | a0001c0001t0006a0001c0001t0007a0001c0002t0048others(1): Show | 13 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5954delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6722 | chr11 | 73400808 | |||||
| chr11:73400897
|
ACTGT | A | 1 | a0001c0001t0002 | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5862_*5865delACAG | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6630 | chr11 | 73400897 | |||||
| chr11:73401009
|
C | T | 1 | a0001c0001t0011 | 3 | HG02895.hp2 HG02897.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5754G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6522 | chr11 | 73401009 | |||||
| chr11:73401046
|
T | C | 7 | a0001c0001t0003a0001c0001t0008a0001c0001t0034others(4): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*5717A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6485 | chr11 | 73401046 | |||||
| chr11:73401080
|
T | TTTA | 14 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(11): Show | 52 | HG00438.hp1 HG00544.hp2 HG01069.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*5680_*5682dupTAA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6450 | chr11 | 73401080 | |||||
| chr11:73401080
|
T | TTTATTA | 11 | a0001c0001t0004a0001c0001t0010a0001c0001t0011others(8): Show | 26 | HG01433.hp2 HG01884.hp1 HG02109.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*5677_*5682dupTAAT others(2): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6450 | chr11 | 73401080 | |||||
| chr11:73401080
|
T | TTTATTAT others(2): Show |
3 | a0001c0001t0018a0001c0001t0025a0001c0001t0029 | 4 | HG02572.hp1 HG02970.hp2 NA19043.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5674_*5682dupTAAT others(5): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6450 | chr11 | 73401080 | |||||
| chr11:73401080
|
T | TTTATTAT others(5): Show |
1 | a0001c0001t0043 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5671_*5682dupTAAT others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6450 | chr11 | 73401080 | |||||
| chr11:73401080
|
T | TTTATTAT others(8): Show |
1 | a0001c0001t0019 | 2 | HG01106.hp2 HG01884.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5668_*5682dupTAAT others(11): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6450 | chr11 | 73401080 | |||||
| chr11:73401080
|
TTTA | T | 6 | a0001c0001t0006a0001c0001t0007a0001c0001t0017others(3): Show | 16 | HG00140.hp2 HG00323.hp1 HG01167.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5680_*5682delTAA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6448 | chr11 | 73401080 | |||||
| chr11:73401260
|
T | C | 2 | a0001c0001t0006a0001c0001t0007 | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5503A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6271 | chr11 | 73401260 | |||||
| chr11:73401375
|
C | T | 1 | a0001c0002t0013 | 3 | HG02258.hp1 HG02647.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5388G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6156 | chr11 | 73401375 | |||||
| chr11:73401376
|
C | A | 2 | a0001c0001t0006a0001c0001t0007 | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5387G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6155 | chr11 | 73401376 | |||||
| chr11:73401376
|
C | G | 2 | a0001c0001t0017a0001c0001t0018 | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5387G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6155 | chr11 | 73401376 | |||||
| chr11:73401378
|
C | G | 1 | a0001c0001t0034 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5385G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6153 | chr11 | 73401378 | |||||
| chr11:73401403
|
C | T | 1 | a0001c0001t0030 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5360G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 6128 | chr11 | 73401403 | |||||
| chr11:73401545
|
C | T | 1 | a0001c0001t0024 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5218G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 5986 | chr11 | 73401545 | |||||
| chr11:73401631
|
G | A | 11 | a0001c0001t0004a0001c0001t0011a0001c0001t0014others(8): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5132C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 5900 | chr11 | 73401631 | |||||
| chr11:73401852
|
G | A | 2 | a0001c0001t0010a0001c0001t0024 | 4 | NA18965.hp1 NA18981.hp1 NA19060.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4911C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 5679 | chr11 | 73401852 | |||||
| chr11:73402072
|
T | C | 6 | a0001c0002t0009a0001c0002t0013a0001c0002t0046others(3): Show | 10 | HG01257.hp2 HG02258.hp1 HG02630.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4691A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 5459 | chr11 | 73402072 | |||||
| chr11:73402493
|
T | C | 1 | a0001c0001t0030 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4270A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 5038 | chr11 | 73402493 | |||||
| chr11:73402717
|
G | A | 1 | a0001c0001t0030 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4046C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 4814 | chr11 | 73402717 | |||||
| chr11:73402758
|
C | T | 2 | a0001c0002t0046a0001c0002t0047 | 2 | NA18906.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4005G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 4773 | chr11 | 73402758 | |||||
| chr11:73402801
|
C | T | 1 | a0001c0002t0045 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3962G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 4730 | chr11 | 73402801 | |||||
| chr11:73402914
|
C | T | 1 | a0001c0001t0030 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3849G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 4617 | chr11 | 73402914 | |||||
| chr11:73403124
|
T | C | 1 | a0001c0002t0031 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3639A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 4407 | chr11 | 73403124 | |||||
| chr11:73403299
|
A | G | 1 | a0001c0001t0030 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3464T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 4232 | chr11 | 73403299 | |||||
| chr11:73403379
|
G | T | 1 | a0001c0002t0044 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3384C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 4152 | chr11 | 73403379 | |||||
| chr11:73403407
|
CT | C | 3 | a0001c0001t0019a0001c0001t0042a0001c0001t0043 | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3355delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 4123 | chr11 | 73403407 | |||||
| chr11:73403448
|
G | T | 1 | a0001c0002t0020 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3315C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 4083 | chr11 | 73403448 | |||||
| chr11:73403564
|
TCTGA | T | 2 | a0001c0001t0010a0001c0001t0024 | 4 | NA18965.hp1 NA18981.hp1 NA19060.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3195_*3198delTCAG | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 3963 | chr11 | 73403564 | |||||
| chr11:73403678
|
A | G | 33 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(30): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*3085T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 3853 | chr11 | 73403678 | |||||
| chr11:73403967
|
G | A | 1 | a0001c0001t0016 | 2 | HG02615.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2796C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 3564 | chr11 | 73403967 | |||||
| chr11:73404159
|
T | C | 1 | a0001c0002t0050 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2604A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 3372 | chr11 | 73404159 | |||||
| chr11:73404220
|
T | C | 11 | a0001c0001t0004a0001c0001t0011a0001c0001t0014others(8): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2543A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 3311 | chr11 | 73404220 | |||||
| chr11:73404269
|
A | G | 25 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(22): Show | 67 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2494T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 3262 | chr11 | 73404269 | |||||
| chr11:73404271
|
C | T | 1 | a0001c0001t0025 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2492G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 3260 | chr11 | 73404271 | |||||
| chr11:73404634
|
A | T | 1 | a0001c0002t0038 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2129T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 2897 | chr11 | 73404634 | |||||
| chr11:73404736
|
G | A | 1 | a0001c0001t0030 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2027C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 2795 | chr11 | 73404736 | |||||
| chr11:73404751
|
T | C | 1 | a0001c0002t0021 | 2 | HG02083.hp2 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2012A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 2780 | chr11 | 73404751 | |||||
| chr11:73404901
|
T | C | 2 | a0001c0001t0006a0001c0001t0007 | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1862A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 2630 | chr11 | 73404901 | |||||
| chr11:73404953
|
C | T | 7 | a0001c0001t0008a0001c0001t0016a0001c0001t0034others(4): Show | 11 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1810G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 2578 | chr11 | 73404953 | |||||
| chr11:73405057
|
C | T | 1 | a0001c0002t0033 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1706G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 2474 | chr11 | 73405057 | |||||
| chr11:73405087
|
T | A | 4 | a0001c0001t0002a0001c0001t0010a0001c0001t0022others(1): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1676A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 2444 | chr11 | 73405087 | |||||
| chr11:73405131
|
G | A | 1 | a0001c0001t0015 | 2 | HG02258.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1632C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 2400 | chr11 | 73405131 | |||||
| chr11:73405251
|
A | G | 1 | a0001c0002t0032 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1512T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 2280 | chr11 | 73405251 | |||||
| chr11:73405316
|
C | T | 4 | a0001c0001t0002a0001c0001t0010a0001c0001t0022others(1): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1447G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 2215 | chr11 | 73405316 | |||||
| chr11:73405403
|
T | TA | 1 | a0001c0001t0007 | 5 | HG01167.hp2 HG01255.hp2 HG01934.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1359dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 2127 | chr11 | 73405403 | |||||
| chr11:73405459
|
C | T | 1 | a0001c0002t0031 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1304G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 2072 | chr11 | 73405459 | |||||
| chr11:73405468
|
T | C | 3 | a0001c0001t0010a0001c0001t0022a0001c0001t0024 | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1295A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 2063 | chr11 | 73405468 | |||||
| chr11:73405502
|
G | C | 1 | a0001c0001t0002 | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1261C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 2029 | chr11 | 73405502 | |||||
| chr11:73405681
|
T | A | 1 | a0001c0002t0023 | 2 | HG01168.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1082A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 1850 | chr11 | 73405681 | |||||
| chr11:73406422
|
C | T | 2 | a0001c0001t0014a0001c0001t0015 | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*341G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 1109 | chr11 | 73406422 | |||||
| chr11:73406516
|
A | G | 11 | a0001c0001t0004a0001c0001t0011a0001c0001t0014others(8): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*247T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 1015 | chr11 | 73406516 | |||||
| chr11:73406543
|
G | C | 1 | a0001c0002t0051 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*220C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 988 | chr11 | 73406543 | |||||
| chr11:73406702
|
G | A | 1 | a0001c0001t0052 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*61C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 8/8 | 829 | chr11 | 73406702 | |||||
| chr11:73597933
|
C | T | 1 | a0001c0001t0002 | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-29G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/8 | 129459 | chr11 | 73597933 | |||||
| chr11:73598069
|
G | T | 2 | a0001c0001t0010a0001c0001t0024 | 4 | NA18965.hp1 NA18981.hp1 NA19060.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-165C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/8 | 129595 | chr11 | 73598069 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:73406749
|
A | G | 1 | a0001c0001t0002g0006 | 1 | HG02922.hp1 | splice_region_variant&intron_variant | LOW | c.*19-5T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 7/7 | chr11 | 73406749 | ||||||
| chr11:73407017
|
A | G | 16 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(13): Show | 16 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.*19-273T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 7/7 | chr11 | 73407017 | ||||||
| chr11:73407279
|
G | A | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.*18+234C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 7/7 | chr11 | 73407279 | ||||||
| chr11:73407316
|
G | A | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.*18+197C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 7/7 | chr11 | 73407316 | ||||||
| chr11:73407376
|
G | A | 1 | a0001c0001t0037g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.*18+137C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 7/7 | chr11 | 73407376 | ||||||
| chr11:73407447
|
C | T | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.*18+66G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 7/7 | chr11 | 73407447 | ||||||
| chr11:73407821
|
G | A | 1 | a0001c0002t0001g0099 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.596-178C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 6/7 | chr11 | 73407821 | ||||||
| chr11:73407825
|
A | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.596-182T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 6/7 | chr11 | 73407825 | ||||||
| chr11:73407895
|
G | A | 2 | a0001c0002t0001g0029a0002c0005t0001g0055 | 2 | HG01069.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.596-252C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 6/7 | chr11 | 73407895 | ||||||
| chr11:73407974
|
C | T | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.596-331G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 6/7 | chr11 | 73407974 | ||||||
| chr11:73408362
|
A | G | 1 | a0001c0001t0024g0003 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.596-719T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 6/7 | chr11 | 73408362 | ||||||
| chr11:73408490
|
G | A | 1 | a0001c0002t0047g0114 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.596-847C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 6/7 | chr11 | 73408490 | ||||||
| chr11:73408780
|
C | CA | 10 | a0001c0001t0003g0162a0001c0001t0003g0166a0001c0001t0010g0001others(7): Show | 10 | HG01106.hp1 HG01978.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.595+706dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 6/7 | chr11 | 73408780 | ||||||
| chr11:73408780
|
C | CAA | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.595+705_595+706dup others(2): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 6/7 | chr11 | 73408780 | ||||||
| chr11:73408834
|
C | A | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.595+653G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 6/7 | chr11 | 73408834 | ||||||
| chr11:73408935
|
T | G | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.595+552A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 6/7 | chr11 | 73408935 | ||||||
| chr11:73409031
|
A | G | 12 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(9): Show | 12 | HG01884.hp1 HG02717.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.595+456T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 6/7 | chr11 | 73409031 | ||||||
| chr11:73409387
|
C | A | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.595+100G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 6/7 | chr11 | 73409387 | ||||||
| chr11:73409433
|
C | T | 4 | a0001c0002t0001g0071a0001c0002t0001g0121a0001c0002t0001g0122others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.595+54G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 6/7 | chr11 | 73409433 | ||||||
| chr11:73410007
|
C | A | 1 | a0001c0001t0041g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.421-346G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 5/7 | chr11 | 73410007 | ||||||
| chr11:73410374
|
C | T | 1 | a0001c0002t0046g0100 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.421-713G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 5/7 | chr11 | 73410374 | ||||||
| chr11:73410827
|
C | G | 63 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(60): Show | 63 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.420+567G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 5/7 | chr11 | 73410827 | ||||||
| chr11:73411295
|
A | G | 58 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(55): Show | 58 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(55): Show |
intron_variant | MODIFIER | c.420+99T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 5/7 | chr11 | 73411295 | ||||||
| chr11:73411857
|
G | A | 1 | a0001c0003t0004g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.278-321C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73411857 | ||||||
| chr11:73411883
|
T | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.278-347A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73411883 | ||||||
| chr11:73411913
|
G | T | 2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.278-377C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73411913 | ||||||
| chr11:73412164
|
CTCATCTT others(38): Show |
C | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.278-673_278-629del others(45): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73412164 | ||||||
| chr11:73412194
|
C | T | 2 | a0001c0001t0003g0158a0001c0001t0003g0165 | 2 | NA18968.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.278-658G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73412194 | ||||||
| chr11:73412467
|
C | T | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.278-931G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73412467 | ||||||
| chr11:73412468
|
G | A | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.278-932C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73412468 | ||||||
| chr11:73412478
|
G | A | 2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.278-942C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73412478 | ||||||
| chr11:73412768
|
A | G | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.278-1232T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73412768 | ||||||
| chr11:73412857
|
C | T | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.278-1321G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73412857 | ||||||
| chr11:73412989
|
G | A | 2 | a0001c0001t0006g0024a0001c0001t0006g0180 | 2 | HG00140.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.278-1453C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73412989 | ||||||
| chr11:73413163
|
C | A | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.278-1627G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73413163 | ||||||
| chr11:73413183
|
CAGG | C | 3 | a0001c0001t0011g0148a0001c0001t0011g0149a0001c0001t0011g0150 | 3 | HG02895.hp2 HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.278-1650_278-1648d others(5): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73413183 | ||||||
| chr11:73413218
|
A | G | 21 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(18): Show | 21 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.278-1682T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73413218 | ||||||
| chr11:73413231
|
T | TC | 179 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.278-1696dupG | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73413231 | ||||||
| chr11:73413386
|
C | T | 1 | a0001c0002t0001g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.278-1850G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73413386 | ||||||
| chr11:73413396
|
A | G | 64 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(61): Show | 64 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.278-1860T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73413396 | ||||||
| chr11:73413514
|
T | A | 1 | a0001c0002t0046g0100 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.278-1978A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73413514 | ||||||
| chr11:73413781
|
A | G | 91 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(88): Show | 91 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.278-2245T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73413781 | ||||||
| chr11:73413850
|
G | A | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-2314C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73413850 | ||||||
| chr11:73413883
|
C | T | 77 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.278-2347G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73413883 | ||||||
| chr11:73413885
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.278-2349C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73413885 | ||||||
| chr11:73414065
|
A | G | 4 | a0001c0002t0001g0071a0001c0002t0001g0121a0001c0002t0001g0122others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-2529T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73414065 | ||||||
| chr11:73414203
|
G | A | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.278-2667C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73414203 | ||||||
| chr11:73414412
|
G | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.278-2876C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73414412 | ||||||
| chr11:73414592
|
G | A | 23 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(20): Show | 23 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.278-3056C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73414592 | ||||||
| chr11:73415505
|
A | G | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.278-3969T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73415505 | ||||||
| chr11:73415688
|
G | A | 1 | a0001c0002t0001g0086 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.278-4152C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73415688 | ||||||
| chr11:73416123
|
T | G | 78 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(75): Show | 78 | HG00140.hp2 HG00323.hp1 HG01106.hp2 others(75): Show |
intron_variant | MODIFIER | c.277+3751A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73416123 | ||||||
| chr11:73416426
|
A | G | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.277+3448T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73416426 | ||||||
| chr11:73416481
|
G | C | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.277+3393C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73416481 | ||||||
| chr11:73417193
|
T | C | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.277+2681A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73417193 | ||||||
| chr11:73417350
|
A | C | 5 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0041g0134others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.277+2524T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73417350 | ||||||
| chr11:73417458
|
C | T | 79 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(76): Show | 79 | HG00140.hp2 HG00323.hp1 HG01106.hp2 others(76): Show |
intron_variant | MODIFIER | c.277+2416G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73417458 | ||||||
| chr11:73417557
|
C | T | 2 | a0001c0001t0017g0032a0001c0001t0017g0078 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.277+2317G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73417557 | ||||||
| chr11:73417559
|
CT | C | 70 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(67): Show | 70 | HG00140.hp2 HG00323.hp1 HG01106.hp2 others(67): Show |
intron_variant | MODIFIER | c.277+2314delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73417559 | ||||||
| chr11:73417802
|
G | A | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.277+2072C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73417802 | ||||||
| chr11:73417940
|
C | T | 2 | a0001c0001t0014g0153a0001c0001t0014g0154 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.277+1934G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73417940 | ||||||
| chr11:73418473
|
G | A | 2 | a0001c0002t0001g0106a0001c0002t0032g0116 | 2 | HG02109.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.277+1401C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73418473 | ||||||
| chr11:73418559
|
C | T | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+1315G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73418559 | ||||||
| chr11:73418585
|
A | G | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.277+1289T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73418585 | ||||||
| chr11:73418589
|
C | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.277+1285G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73418589 | ||||||
| chr11:73418669
|
C | G | 3 | a0001c0001t0025g0120a0001c0001t0039g0125a0001c0001t0040g0126 | 3 | HG02055.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.277+1205G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73418669 | ||||||
| chr11:73418701
|
A | G | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.277+1173T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73418701 | ||||||
| chr11:73418809
|
A | AT | 8 | a0001c0001t0003g0169a0001c0001t0003g0171a0001c0001t0008g0172others(5): Show | 8 | HG01515.hp2 HG02615.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.277+1064dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73418809 | ||||||
| chr11:73418809
|
AT | A | 61 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(58): Show | 61 | HG00140.hp2 HG00323.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.277+1064delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73418809 | ||||||
| chr11:73418815
|
T | A | 1 | a0001c0002t0001g0046 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.277+1059A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73418815 | ||||||
| chr11:73418847
|
C | T | 24 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(21): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.277+1027G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73418847 | ||||||
| chr11:73418861
|
T | G | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.277+1013A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73418861 | ||||||
| chr11:73418957
|
C | T | 3 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0091 | 3 | HG02622.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.277+917G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73418957 | ||||||
| chr11:73418958
|
A | G | 3 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0091 | 3 | HG02622.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.277+916T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73418958 | ||||||
| chr11:73419014
|
G | A | 3 | a0001c0002t0009g0073a0001c0002t0049g0072a0001c0004t0009g0074 | 3 | HG02630.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.277+860C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73419014 | ||||||
| chr11:73419046
|
G | A | 2 | a0001c0001t0017g0032a0001c0001t0017g0078 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.277+828C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73419046 | ||||||
| chr11:73419090
|
A | G | 16 | a0001c0002t0001g0053a0001c0002t0001g0094a0001c0002t0001g0106others(13): Show | 16 | HG00140.hp1 HG00323.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.277+784T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73419090 | ||||||
| chr11:73419102
|
G | A | 1 | a0001c0002t0001g0042 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.277+772C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73419102 | ||||||
| chr11:73419105
|
C | T | 23 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(20): Show | 23 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.277+769G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73419105 | ||||||
| chr11:73419195
|
C | A | 1 | a0001c0002t0001g0097 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.277+679G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73419195 | ||||||
| chr11:73419355
|
C | T | 23 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(20): Show | 23 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.277+519G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73419355 | ||||||
| chr11:73419390
|
A | G | 1 | a0001c0001t0037g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.277+484T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73419390 | ||||||
| chr11:73419393
|
A | C | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.277+481T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 4/7 | chr11 | 73419393 | ||||||
| chr11:73420150
|
T | C | 7 | a0001c0001t0008g0159a0001c0001t0008g0172a0001c0001t0008g0173others(4): Show | 7 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.152-151A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73420150 | ||||||
| chr11:73420553
|
A | G | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-554T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73420553 | ||||||
| chr11:73420745
|
GA | G | 2 | a0001c0002t0001g0095a0001c0002t0001g0122 | 2 | HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.152-747delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73420745 | ||||||
| chr11:73420809
|
C | T | 1 | a0001c0002t0001g0115 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.152-810G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73420809 | ||||||
| chr11:73420934
|
A | T | 1 | a0001c0002t0001g0089 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.152-935T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73420934 | ||||||
| chr11:73421071
|
T | TG | 30 | a0001c0001t0004g0142a0001c0001t0004g0143a0001c0001t0004g0145others(27): Show | 30 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.152-1073dupC | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73421071 | ||||||
| chr11:73421072
|
G | GC | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-1074_152-1073i others(3): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73421072 | ||||||
| chr11:73421075
|
G | GGC | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.152-1077_152-1076i others(4): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73421075 | ||||||
| chr11:73421266
|
T | C | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.152-1267A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73421266 | ||||||
| chr11:73421403
|
G | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.152-1404C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73421403 | ||||||
| chr11:73421564
|
T | A | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.152-1565A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73421564 | ||||||
| chr11:73421615
|
TG | T | 79 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(76): Show | 79 | HG00140.hp2 HG00323.hp1 HG01106.hp2 others(76): Show |
intron_variant | MODIFIER | c.152-1617delC | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73421615 | ||||||
| chr11:73421728
|
C | A | 1 | a0001c0001t0039g0125 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.152-1729G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73421728 | ||||||
| chr11:73421985
|
T | C | 58 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(55): Show | 58 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(55): Show |
intron_variant | MODIFIER | c.152-1986A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73421985 | ||||||
| chr11:73422259
|
C | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.152-2260G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73422259 | ||||||
| chr11:73422260
|
T | G | 2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.152-2261A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73422260 | ||||||
| chr11:73422314
|
T | G | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-2315A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73422314 | ||||||
| chr11:73422369
|
G | A | 1 | a0001c0002t0009g0076 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.152-2370C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73422369 | ||||||
| chr11:73422378
|
T | C | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-2379A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73422378 | ||||||
| chr11:73422536
|
C | G | 3 | a0001c0001t0025g0120a0001c0001t0039g0125a0001c0001t0040g0126 | 3 | HG02055.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.152-2537G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73422536 | ||||||
| chr11:73422605
|
G | C | 9 | a0001c0001t0008g0159a0001c0001t0008g0172a0001c0001t0008g0173others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-2606C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73422605 | ||||||
| chr11:73422787
|
CGA | C | 58 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(55): Show | 58 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(55): Show |
intron_variant | MODIFIER | c.152-2790_152-2789d others(4): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73422787 | ||||||
| chr11:73423195
|
C | T | 23 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(20): Show | 23 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.152-3196G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73423195 | ||||||
| chr11:73423353
|
C | T | 10 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-3354G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73423353 | ||||||
| chr11:73423633
|
A | G | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.152-3634T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73423633 | ||||||
| chr11:73423964
|
G | T | 1 | a0001c0002t0001g0096 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.152-3965C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73423964 | ||||||
| chr11:73424186
|
A | G | 15 | a0001c0002t0001g0053a0001c0002t0001g0094a0001c0002t0001g0106others(12): Show | 15 | HG00140.hp1 HG00323.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.152-4187T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73424186 | ||||||
| chr11:73424290
|
A | T | 2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.152-4291T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73424290 | ||||||
| chr11:73424490
|
C | T | 4 | a0001c0001t0004g0143a0001c0001t0004g0145a0001c0001t0026g0144others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-4491G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73424490 | ||||||
| chr11:73424502
|
C | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.152-4503G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73424502 | ||||||
| chr11:73424643
|
T | G | 1 | a0001c0002t0001g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.152-4644A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73424643 | ||||||
| chr11:73424663
|
A | T | 1 | a0001c0002t0001g0065 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.152-4664T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73424663 | ||||||
| chr11:73424969
|
G | A | 1 | a0001c0002t0001g0046 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.152-4970C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73424969 | ||||||
| chr11:73425216
|
A | T | 55 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(52): Show | 55 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(52): Show |
intron_variant | MODIFIER | c.152-5217T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73425216 | ||||||
| chr11:73425300
|
G | A | 1 | a0001c0001t0022g0062 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.152-5301C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73425300 | ||||||
| chr11:73425437
|
T | C | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+5253A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73425437 | ||||||
| chr11:73425460
|
T | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+5230A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73425460 | ||||||
| chr11:73425486
|
G | C | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+5204C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73425486 | ||||||
| chr11:73425896
|
T | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.151+4794A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73425896 | ||||||
| chr11:73425950
|
A | G | 2 | a0001c0002t0001g0065a0001c0002t0001g0066 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.151+4740T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73425950 | ||||||
| chr11:73426019
|
C | A | 1 | a0001c0002t0001g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.151+4671G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73426019 | ||||||
| chr11:73426256
|
C | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+4434G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73426256 | ||||||
| chr11:73426317
|
A | G | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.151+4373T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73426317 | ||||||
| chr11:73426338
|
T | A | 1 | a0001c0002t0005g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.151+4352A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73426338 | ||||||
| chr11:73426703
|
C | CTG | 12 | a0001c0001t0039g0125a0001c0001t0040g0126a0001c0002t0001g0052others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.151+3985_151+3986d others(4): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73426703 | ||||||
| chr11:73426703
|
C | CTGTG | 19 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(16): Show | 19 | HG00438.hp1 HG00544.hp2 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.151+3983_151+3986d others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73426703 | ||||||
| chr11:73426703
|
C | CTGTGTG | 12 | a0001c0001t0004g0143a0001c0001t0004g0145a0001c0001t0011g0148others(9): Show | 12 | HG01106.hp2 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+3981_151+3986d others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73426703 | ||||||
| chr11:73426703
|
C | CTGTGTGT others(1): Show |
7 | a0001c0001t0002g0008a0001c0001t0004g0137a0001c0001t0004g0138others(4): Show | 7 | HG01884.hp1 HG02965.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+3979_151+3986d others(10): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73426703 | ||||||
| chr11:73426703
|
C | CTGTGTGT others(5): Show |
14 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(11): Show | 14 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+3975_151+3986d others(14): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73426703 | ||||||
| chr11:73426703
|
C | CTGTGTGT others(7): Show |
7 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(4): Show | 7 | HG00140.hp2 HG01255.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+3973_151+3986d others(16): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73426703 | ||||||
| chr11:73426703
|
C | CTGTGTGT others(9): Show |
2 | a0001c0001t0010g0002a0001c0001t0022g0061 | 2 | HG02818.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.151+3971_151+3986d others(18): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73426703 | ||||||
| chr11:73426703
|
C | CTGTGTGT others(11): Show |
5 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0007g0026others(2): Show | 5 | HG01167.hp2 HG01934.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.151+3969_151+3986d others(20): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73426703 | ||||||
| chr11:73426703
|
C | CTGTGTGT others(13): Show |
2 | a0001c0001t0010g0001a0001c0001t0022g0062 | 2 | HG02622.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.151+3967_151+3986d others(22): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73426703 | ||||||
| chr11:73426703
|
C | CTGTGTGT others(15): Show |
1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.151+3965_151+3986d others(24): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73426703 | ||||||
| chr11:73426703
|
C | CTGTGTGT others(21): Show |
1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.151+3959_151+3986d others(30): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73426703 | ||||||
| chr11:73426703
|
CTG | C | 3 | a0001c0001t0016g0136a0001c0002t0001g0080a0001c0002t0045g0112 | 3 | HG02040.hp1 HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.151+3985_151+3986d others(4): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73426703 | ||||||
| chr11:73426703
|
CTGTG | C | 13 | a0001c0001t0008g0159a0001c0001t0008g0172a0001c0001t0008g0173others(10): Show | 13 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.151+3983_151+3986d others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73426703 | ||||||
| chr11:73427281
|
G | A | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.151+3409C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73427281 | ||||||
| chr11:73427282
|
C | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+3408G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73427282 | ||||||
| chr11:73427349
|
AC | A | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+3340delG | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73427349 | ||||||
| chr11:73427351
|
T | A | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+3339A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73427351 | ||||||
| chr11:73427381
|
A | AT | 55 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(52): Show | 55 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(52): Show |
intron_variant | MODIFIER | c.151+3308_151+3309i others(3): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73427381 | ||||||
| chr11:73427830
|
G | A | 1 | a0001c0002t0001g0046 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.151+2860C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73427830 | ||||||
| chr11:73427887
|
A | G | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.151+2803T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73427887 | ||||||
| chr11:73428071
|
T | C | 55 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(52): Show | 55 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(52): Show |
intron_variant | MODIFIER | c.151+2619A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73428071 | ||||||
| chr11:73428331
|
A | T | 10 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+2359T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73428331 | ||||||
| chr11:73428540
|
T | C | 3 | a0001c0001t0025g0120a0001c0001t0039g0125a0001c0001t0040g0126 | 3 | HG02055.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.151+2150A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73428540 | ||||||
| chr11:73428604
|
A | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.151+2086T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73428604 | ||||||
| chr11:73428737
|
G | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.151+1953C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73428737 | ||||||
| chr11:73429093
|
T | A | 93 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(90): Show | 93 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.151+1597A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73429093 | ||||||
| chr11:73429288
|
A | G | 1 | a0001c0002t0005g0155 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.151+1402T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73429288 | ||||||
| chr11:73429438
|
G | A | 1 | a0001c0002t0001g0039 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.151+1252C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73429438 | ||||||
| chr11:73429658
|
T | C | 1 | a0001c0002t0033g0077 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.151+1032A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73429658 | ||||||
| chr11:73429849
|
T | C | 1 | a0001c0001t0003g0171 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.151+841A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73429849 | ||||||
| chr11:73430246
|
A | ATG | 15 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(12): Show | 15 | HG01069.hp1 HG01069.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.151+442_151+443dup others(2): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73430246 | ||||||
| chr11:73430246
|
A | ATGTG | 27 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(24): Show | 27 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.151+440_151+443dup others(4): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73430246 | ||||||
| chr11:73430246
|
A | ATGTGTG | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+438_151+443dup others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73430246 | ||||||
| chr11:73430246
|
ATG | A | 45 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(42): Show | 45 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.151+442_151+443del others(2): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73430246 | ||||||
| chr11:73430246
|
ATGTGTGT others(25): Show |
A | 1 | a0001c0002t0001g0042 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.151+412_151+443del others(32): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73430246 | ||||||
| chr11:73430277
|
G | GGT | 19 | a0001c0001t0002g0017a0001c0001t0004g0143a0001c0001t0004g0145others(16): Show | 19 | HG02258.hp2 HG02451.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.151+411_151+412dup others(2): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73430277 | ||||||
| chr11:73430277
|
G | GGTGT | 27 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(24): Show | 27 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(24): Show |
intron_variant | MODIFIER | c.151+409_151+412dup others(4): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73430277 | ||||||
| chr11:73430277
|
GGT | G | 16 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(13): Show | 16 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.151+411_151+412del others(2): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73430277 | ||||||
| chr11:73430277
|
GGTGT | G | 3 | a0001c0002t0032g0116a0001c0003t0004g0063a0001c0003t0028g0064 | 3 | HG02109.hp1 HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.151+409_151+412del others(4): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73430277 | ||||||
| chr11:73430277
|
GGTGTGTG others(3): Show |
G | 1 | a0001c0002t0005g0155 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.151+403_151+412del others(10): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73430277 | ||||||
| chr11:73430312
|
G | T | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.151+378C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73430312 | ||||||
| chr11:73430325
|
T | G | 9 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(6): Show | 9 | HG01884.hp1 HG02717.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+365A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73430325 | ||||||
| chr11:73430390
|
T | C | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.151+300A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73430390 | ||||||
| chr11:73430581
|
G | A | 4 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(1): Show | 4 | HG01884.hp1 HG03130.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+109C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73430581 | ||||||
| chr11:73430582
|
C | G | 58 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(55): Show | 58 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(55): Show |
intron_variant | MODIFIER | c.151+108G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73430582 | ||||||
| chr11:73430663
|
G | A | 1 | a0001c0002t0009g0076 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.151+27C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | 73430663 | ||||||
| chr11:73430810
|
A | C | 1 | a0001c0003t0004g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.71-40T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73430810 | ||||||
| chr11:73430810
|
AAAAACAA others(3): Show |
A | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.71-50_71-41delGTTT others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73430810 | ||||||
| chr11:73430814
|
A | C | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-44T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73430814 | ||||||
| chr11:73431387
|
A | G | 1 | a0001c0002t0009g0073 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.71-617T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73431387 | ||||||
| chr11:73431420
|
C | T | 1 | a0001c0002t0001g0096 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.71-650G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73431420 | ||||||
| chr11:73431512
|
CAT | C | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-744_71-743delAT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73431512 | ||||||
| chr11:73431514
|
T | C | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-744A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73431514 | ||||||
| chr11:73431612
|
G | A | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-842C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73431612 | ||||||
| chr11:73431630
|
T | C | 25 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(22): Show | 25 | HG01884.hp1 HG02109.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.71-860A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73431630 | ||||||
| chr11:73431669
|
A | G | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-899T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73431669 | ||||||
| chr11:73431679
|
A | G | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.71-909T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73431679 | ||||||
| chr11:73431756
|
A | AT | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.71-987dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73431756 | ||||||
| chr11:73431929
|
A | G | 2 | a0001c0001t0006g0024a0001c0001t0006g0180 | 2 | HG00140.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.71-1159T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73431929 | ||||||
| chr11:73432092
|
A | G | 23 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(20): Show | 23 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.71-1322T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73432092 | ||||||
| chr11:73432112
|
C | T | 7 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(4): Show | 7 | HG01255.hp1 HG01257.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.71-1342G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73432112 | ||||||
| chr11:73432439
|
T | TTTA | 5 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(2): Show | 5 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-1672_71-1670dup others(3): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73432439 | ||||||
| chr11:73432439
|
TTTA | T | 5 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0041g0134others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-1672_71-1670del others(3): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73432439 | ||||||
| chr11:73432717
|
G | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.71-1947C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73432717 | ||||||
| chr11:73432740
|
C | T | 1 | a0001c0002t0001g0065 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.71-1970G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73432740 | ||||||
| chr11:73432839
|
C | T | 1 | a0001c0001t0022g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.71-2069G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73432839 | ||||||
| chr11:73432986
|
A | T | 1 | a0001c0002t0033g0077 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.71-2216T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73432986 | ||||||
| chr11:73433049
|
C | T | 23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.71-2279G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433049 | ||||||
| chr11:73433068
|
C | CA | 2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.71-2299_71-2298ins others(1): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433068 | ||||||
| chr11:73433069
|
G | A | 2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.71-2299C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433069 | ||||||
| chr11:73433076
|
C | CT | 32 | a0001c0001t0003g0165a0001c0001t0003g0166a0001c0001t0003g0169others(29): Show | 32 | HG00438.hp2 HG00544.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.71-2307dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433076 | ||||||
| chr11:73433076
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0004g0138a0001c0001t0004g0139 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.71-2316_71-2307dup others(10): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433076 | ||||||
| chr11:73433076
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0004g0137a0001c0001t0004g0143a0001c0001t0004g0145others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-2317_71-2307dup others(11): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433076 | ||||||
| chr11:73433076
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0029g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.71-2319_71-2307dup others(13): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433076 | ||||||
| chr11:73433076
|
C | CTTTTTTT others(15): Show |
3 | a0001c0001t0004g0142a0001c0001t0004g0147a0001c0001t0027g0146 | 3 | HG02717.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.71-2328_71-2307dup others(22): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433076 | ||||||
| chr11:73433076
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0014g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.71-2332_71-2307dup others(26): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433076 | ||||||
| chr11:73433076
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0004g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.71-2333_71-2307dup others(27): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433076 | ||||||
| chr11:73433076
|
CT | C | 24 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(21): Show | 24 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.71-2307delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433076 | ||||||
| chr11:73433076
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.71-2316_71-2307del others(10): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433076 | ||||||
| chr11:73433359
|
C | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-2589G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433359 | ||||||
| chr11:73433367
|
C | CA | 7 | a0001c0001t0015g0132a0001c0001t0015g0133a0001c0001t0025g0120others(4): Show | 7 | HG02258.hp2 HG03195.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.71-2598dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433367 | ||||||
| chr11:73433367
|
CA | C | 65 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(62): Show | 65 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.71-2598delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433367 | ||||||
| chr11:73433664
|
A | G | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.71-2894T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433664 | ||||||
| chr11:73433779
|
G | C | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-3009C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433779 | ||||||
| chr11:73433840
|
CT | C | 63 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(60): Show | 63 | HG00140.hp1 HG00323.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.71-3071delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433840 | ||||||
| chr11:73433840
|
CTT | C | 44 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(41): Show | 44 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.71-3072_71-3071del others(2): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433840 | ||||||
| chr11:73433840
|
CTTT | C | 23 | a0001c0001t0003g0166a0001c0001t0004g0137a0001c0001t0004g0138others(20): Show | 23 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.71-3073_71-3071del others(3): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433840 | ||||||
| chr11:73433939
|
G | A | 1 | a0001c0002t0033g0077 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.71-3169C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433939 | ||||||
| chr11:73433994
|
T | C | 1 | a0001c0002t0033g0077 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.71-3224A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73433994 | ||||||
| chr11:73434134
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.71-3364C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73434134 | ||||||
| chr11:73434386
|
G | GT | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-3617dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73434386 | ||||||
| chr11:73434553
|
G | A | 1 | a0001c0001t0003g0162 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.71-3783C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73434553 | ||||||
| chr11:73435077
|
TC | T | 3 | a0001c0001t0004g0142a0001c0001t0004g0147a0001c0001t0027g0146 | 3 | HG02717.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.71-4308delG | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73435077 | ||||||
| chr11:73435891
|
T | C | 3 | a0001c0001t0004g0142a0001c0001t0004g0147a0001c0001t0027g0146 | 3 | HG02717.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.71-5121A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73435891 | ||||||
| chr11:73436015
|
T | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.71-5245A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73436015 | ||||||
| chr11:73436051
|
A | T | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.71-5281T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73436051 | ||||||
| chr11:73436103
|
C | CT | 24 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(21): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.71-5334dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73436103 | ||||||
| chr11:73436428
|
A | G | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-5658T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73436428 | ||||||
| chr11:73436517
|
AT | A | 179 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.71-5748delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73436517 | ||||||
| chr11:73436522
|
C | CA | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.71-5753dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73436522 | ||||||
| chr11:73436534
|
C | A | 2 | a0001c0001t0017g0032a0001c0001t0017g0078 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.71-5764G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73436534 | ||||||
| chr11:73436541
|
C | T | 4 | a0001c0002t0001g0071a0001c0002t0001g0121a0001c0002t0001g0122others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-5771G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73436541 | ||||||
| chr11:73436895
|
T | C | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-6125A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73436895 | ||||||
| chr11:73436929
|
T | C | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-6159A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73436929 | ||||||
| chr11:73436999
|
T | C | 1 | a0001c0001t0041g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.71-6229A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73436999 | ||||||
| chr11:73437101
|
C | CT | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.71-6332dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73437101 | ||||||
| chr11:73437101
|
CTT | C | 23 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(20): Show | 23 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.71-6333_71-6332del others(2): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73437101 | ||||||
| chr11:73437345
|
C | G | 1 | a0001c0002t0032g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.71-6575G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73437345 | ||||||
| chr11:73437400
|
C | CT | 19 | a0001c0001t0006g0067a0001c0001t0007g0027a0001c0001t0022g0061others(16): Show | 19 | HG00140.hp1 HG00323.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.71-6631dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73437400 | ||||||
| chr11:73437400
|
C | CTT | 8 | a0001c0001t0006g0024a0001c0001t0006g0180a0001c0001t0007g0026others(5): Show | 8 | HG00140.hp2 HG02622.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-6632_71-6631dup others(2): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73437400 | ||||||
| chr11:73437400
|
C | CTTT | 6 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0028others(3): Show | 6 | HG01167.hp2 HG01255.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-6633_71-6631dup others(3): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73437400 | ||||||
| chr11:73437400
|
CT | C | 53 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(50): Show | 53 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.71-6631delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73437400 | ||||||
| chr11:73437453
|
A | G | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.71-6683T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73437453 | ||||||
| chr11:73437497
|
C | A | 1 | a0001c0001t0002g0011 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.71-6727G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73437497 | ||||||
| chr11:73437589
|
T | A | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-6819A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73437589 | ||||||
| chr11:73437739
|
G | A | 1 | a0001c0002t0050g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.71-6969C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73437739 | ||||||
| chr11:73437744
|
C | T | 1 | a0001c0001t0014g0154 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.71-6974G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73437744 | ||||||
| chr11:73437759
|
T | TAG | 10 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.71-6991_71-6990dup others(2): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73437759 | ||||||
| chr11:73437826
|
G | T | 23 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(20): Show | 23 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.71-7056C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73437826 | ||||||
| chr11:73438038
|
G | A | 1 | a0001c0002t0001g0099 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.71-7268C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73438038 | ||||||
| chr11:73438053
|
T | C | 3 | a0001c0002t0005g0047a0001c0002t0005g0048a0001c0002t0038g0041 | 3 | HG01928.hp1 HG01934.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.71-7283A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73438053 | ||||||
| chr11:73438245
|
C | A | 2 | a0001c0001t0014g0153a0001c0001t0014g0154 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.71-7475G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73438245 | ||||||
| chr11:73438745
|
T | C | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.71-7975A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73438745 | ||||||
| chr11:73438896
|
CAAAGAAT others(1): Show |
C | 8 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-8134_71-8127del others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73438896 | ||||||
| chr11:73438907
|
G | A | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.71-8137C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73438907 | ||||||
| chr11:73438958
|
C | G | 4 | a0001c0001t0011g0148a0001c0001t0011g0149a0001c0001t0011g0150others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-8188G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73438958 | ||||||
| chr11:73438994
|
T | C | 1 | a0001c0002t0001g0046 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.71-8224A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73438994 | ||||||
| chr11:73439435
|
G | C | 1 | a0001c0002t0049g0072 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71-8665C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73439435 | ||||||
| chr11:73439579
|
T | G | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.71-8809A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73439579 | ||||||
| chr11:73439788
|
T | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.71-9018A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73439788 | ||||||
| chr11:73439879
|
C | CT | 52 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(49): Show | 52 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.71-9110dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73439879 | ||||||
| chr11:73439879
|
C | CTT | 14 | a0001c0001t0003g0171a0001c0001t0006g0020a0001c0001t0006g0021others(11): Show | 14 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.71-9111_71-9110dup others(2): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73439879 | ||||||
| chr11:73439879
|
CT | C | 16 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(13): Show | 16 | HG01106.hp2 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.71-9110delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73439879 | ||||||
| chr11:73439907
|
C | T | 3 | a0001c0001t0025g0120a0001c0001t0039g0125a0001c0001t0040g0126 | 3 | HG02055.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.71-9137G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73439907 | ||||||
| chr11:73440082
|
C | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.71-9312G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73440082 | ||||||
| chr11:73440290
|
T | G | 23 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(20): Show | 23 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.71-9520A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73440290 | ||||||
| chr11:73440302
|
C | A | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.71-9532G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73440302 | ||||||
| chr11:73440729
|
T | C | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-9959A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73440729 | ||||||
| chr11:73441062
|
C | CT | 69 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(66): Show | 69 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.71-10293dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73441062 | ||||||
| chr11:73441062
|
C | CTT | 22 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(19): Show | 22 | HG02055.hp2 HG02258.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.71-10294_71-10293d others(4): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73441062 | ||||||
| chr11:73441471
|
T | C | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.71-10701A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73441471 | ||||||
| chr11:73441610
|
A | G | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.71-10840T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73441610 | ||||||
| chr11:73441669
|
T | G | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.71-10899A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73441669 | ||||||
| chr11:73442125
|
CT | C | 54 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(51): Show | 54 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.71-11356delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442125 | ||||||
| chr11:73442215
|
T | C | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-11445A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442215 | ||||||
| chr11:73442348
|
G | A | 4 | a0001c0002t0001g0094a0001c0002t0001g0118a0001c0002t0012g0082others(1): Show | 4 | HG02040.hp2 NA18984.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-11578C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442348 | ||||||
| chr11:73442360
|
T | C | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-11590A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442360 | ||||||
| chr11:73442689
|
T | C | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-11919A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442689 | ||||||
| chr11:73442838
|
C | CT | 8 | a0001c0001t0004g0142a0001c0001t0004g0143a0001c0001t0004g0145others(5): Show | 8 | HG02027.hp1 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-12069dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442838 | ||||||
| chr11:73442838
|
C | CTT | 21 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(18): Show | 21 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.71-12070_71-12069d others(4): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442838 | ||||||
| chr11:73442838
|
CT | C | 14 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(11): Show | 14 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.71-12069delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442838 | ||||||
| chr11:73442842
|
T | C | 1 | a0001c0001t0036g0178 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.71-12072A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442842 | ||||||
| chr11:73442955
|
G | GAT | 26 | a0001c0001t0003g0167a0001c0001t0004g0138a0001c0001t0004g0142others(23): Show | 26 | HG00544.hp1 HG00544.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.71-12187_71-12186d others(4): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
G | GATAT | 32 | a0001c0001t0003g0176a0001c0001t0006g0020a0001c0001t0006g0028others(29): Show | 32 | HG00140.hp1 HG00438.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.71-12189_71-12186d others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
G | GATATAT | 19 | a0001c0001t0003g0161a0001c0001t0003g0162a0001c0001t0003g0169others(16): Show | 19 | HG01257.hp2 HG01517.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.71-12191_71-12186d others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
G | GATATATA others(1): Show |
19 | a0001c0001t0003g0164a0001c0001t0003g0168a0001c0001t0004g0140others(16): Show | 19 | HG00323.hp1 HG00438.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.71-12193_71-12186d others(10): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
G | GATATATA others(3): Show |
6 | a0001c0001t0003g0158a0001c0001t0003g0165a0001c0001t0004g0139others(3): Show | 6 | HG01884.hp1 HG02895.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-12195_71-12186d others(12): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
G | GATATATA others(5): Show |
11 | a0001c0001t0003g0160a0001c0001t0003g0166a0001c0001t0003g0170others(8): Show | 11 | HG01168.hp2 HG01433.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.71-12197_71-12186d others(14): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
G | GATATATA others(7): Show |
3 | a0001c0001t0003g0171a0001c0002t0001g0097a0001c0002t0005g0048 | 3 | HG01934.hp1 NA18977.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.71-12199_71-12186d others(16): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
G | GATATATA others(9): Show |
2 | a0001c0002t0001g0035a0001c0002t0001g0127 | 2 | HG02976.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.71-12201_71-12186d others(18): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
G | GATATATA others(11): Show |
1 | a0001c0001t0003g0163 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.71-12203_71-12186d others(20): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
G | GATATATA others(13): Show |
1 | a0001c0002t0001g0058 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.71-12205_71-12186d others(22): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
GAT | G | 7 | a0001c0001t0006g0024a0001c0001t0006g0067a0001c0001t0039g0125others(4): Show | 7 | HG00140.hp2 HG02055.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.71-12187_71-12186d others(4): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
GATAT | G | 4 | a0001c0001t0004g0145a0001c0001t0017g0032a0001c0001t0024g0003others(1): Show | 4 | HG02055.hp1 HG02717.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-12189_71-12186d others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
GATATAT | G | 5 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0016g0136others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-12191_71-12186d others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
GATATATA others(1): Show |
G | 7 | a0001c0001t0004g0143a0001c0001t0017g0078a0001c0001t0026g0144others(4): Show | 7 | HG02559.hp2 HG02572.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-12193_71-12186d others(10): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
GATATATA others(3): Show |
G | 1 | a0001c0002t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.71-12195_71-12186d others(12): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
GATATATA others(5): Show |
G | 2 | a0001c0001t0014g0153a0001c0001t0014g0154 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.71-12197_71-12186d others(14): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
GATATATA others(7): Show |
G | 2 | a0001c0001t0010g0004a0001c0002t0032g0116 | 2 | HG02109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.71-12199_71-12186d others(16): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
GATATATA others(9): Show |
G | 3 | a0001c0001t0015g0132a0001c0001t0015g0133a0001c0002t0005g0085 | 3 | HG01069.hp1 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.71-12201_71-12186d others(18): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
GATATATA others(11): Show |
G | 1 | a0001c0002t0051g0108 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.71-12203_71-12186d others(20): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
GATATATA others(15): Show |
G | 1 | a0001c0001t0041g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.71-12207_71-12186d others(24): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
GATATATA others(17): Show |
G | 1 | a0001c0002t0001g0033 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.71-12209_71-12186d others(26): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442955
|
GATATATA others(21): Show |
G | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.71-12213_71-12186d others(30): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442955 | ||||||
| chr11:73442995
|
T | C | 1 | a0001c0001t0024g0003 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.71-12225A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73442995 | ||||||
| chr11:73443083
|
G | A | 1 | a0001c0003t0004g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.71-12313C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73443083 | ||||||
| chr11:73443143
|
T | C | 1 | a0001c0002t0001g0089 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.71-12373A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73443143 | ||||||
| chr11:73443237
|
C | T | 1 | a0001c0001t0002g0017 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.71-12467G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73443237 | ||||||
| chr11:73443528
|
G | A | 3 | a0001c0001t0025g0120a0001c0001t0039g0125a0001c0001t0040g0126 | 3 | HG02055.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.71-12758C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73443528 | ||||||
| chr11:73443605
|
C | T | 27 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(24): Show | 27 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.71-12835G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73443605 | ||||||
| chr11:73443653
|
G | C | 2 | a0001c0001t0004g0151a0001c0001t0004g0152 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.71-12883C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73443653 | ||||||
| chr11:73443684
|
G | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-12914C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73443684 | ||||||
| chr11:73443932
|
A | C | 1 | a0001c0001t0003g0167 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.71-13162T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73443932 | ||||||
| chr11:73444027
|
T | C | 27 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(24): Show | 27 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.71-13257A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73444027 | ||||||
| chr11:73444779
|
G | A | 1 | a0001c0002t0033g0077 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.71-14009C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73444779 | ||||||
| chr11:73445176
|
T | C | 1 | a0001c0001t0034g0174 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.71-14406A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445176 | ||||||
| chr11:73445196
|
T | A | 1 | a0001c0001t0022g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.71-14426A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445196 | ||||||
| chr11:73445259
|
C | CA | 20 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(17): Show | 20 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(17): Show |
intron_variant | MODIFIER | c.71-14490dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445259 | ||||||
| chr11:73445419
|
C | CT | 14 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0065others(11): Show | 14 | HG01106.hp1 HG01109.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.71-14650dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
C | CTCTCTCT others(2): Show |
5 | a0001c0001t0010g0002a0001c0001t0010g0004a0001c0001t0022g0061others(2): Show | 5 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-14650_71-14649i others(11): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
C | CTCTCTCT others(3): Show |
1 | a0001c0001t0010g0001 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.71-14650_71-14649i others(12): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0003g0161a0001c0001t0003g0168a0001c0001t0003g0176others(3): Show | 6 | HG00438.hp1 HG01261.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-14659_71-14650d others(12): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0003g0169a0001c0001t0003g0171a0001c0001t0008g0159others(1): Show | 4 | HG01168.hp2 HG03831.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-14660_71-14650d others(13): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
C | CTTTTTTT others(5): Show |
5 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0001t0003g0164others(2): Show | 5 | HG01928.hp2 HG01978.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-14661_71-14650d others(14): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0003g0160a0001c0001t0052g0157 | 2 | HG03710.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.71-14662_71-14650d others(15): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0035g0179 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.71-14663_71-14650d others(16): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0043g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.71-14664_71-14650d others(17): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
C | CTTTTTTT others(10): Show |
3 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060 | 3 | HG01106.hp2 HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.71-14666_71-14650d others(19): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0003g0170a0001c0001t0016g0136 | 2 | HG02615.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.71-14667_71-14650d others(20): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.71-14668_71-14650d others(21): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
C | CTTTTTTT others(13): Show |
5 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0015others(2): Show | 5 | HG02451.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-14669_71-14650d others(22): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
C | CTTTTTTT others(14): Show |
5 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0012others(2): Show | 5 | HG01433.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-14670_71-14650d others(23): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
C | CTTTTTTT others(15): Show |
2 | a0001c0001t0002g0009a0001c0001t0002g0014 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.71-14671_71-14650d others(24): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0002g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.71-14675_71-14650d others(28): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
CT | C | 32 | a0001c0001t0039g0125a0001c0002t0001g0031a0001c0002t0001g0042others(29): Show | 32 | HG00140.hp1 HG00323.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.71-14650delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
CTTTT | C | 5 | a0001c0001t0006g0020a0001c0001t0007g0022a0001c0001t0007g0023others(2): Show | 5 | HG01167.hp2 HG01934.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-14653_71-14650d others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
CTTTTT | C | 7 | a0001c0001t0003g0167a0001c0001t0006g0021a0001c0001t0006g0024others(4): Show | 7 | HG00140.hp2 HG00544.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-14654_71-14650d others(7): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
CTTTTTTT others(1): Show |
C | 22 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0004g0137others(19): Show | 22 | HG01884.hp1 HG02258.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.71-14657_71-14650d others(10): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445419
|
CTTTTTTT others(7): Show |
C | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-14663_71-14650d others(16): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445419 | ||||||
| chr11:73445421
|
T | C | 1 | a0001c0002t0048g0043 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.71-14651A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445421 | ||||||
| chr11:73445451
|
G | A | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.71-14681C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445451 | ||||||
| chr11:73445461
|
G | A | 1 | a0001c0002t0005g0059 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.71-14691C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445461 | ||||||
| chr11:73445891
|
C | T | 3 | a0001c0001t0025g0120a0001c0001t0039g0125a0001c0001t0040g0126 | 3 | HG02055.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.71-15121G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73445891 | ||||||
| chr11:73446192
|
ATCT | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.71-15425_71-15423d others(5): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73446192 | ||||||
| chr11:73446564
|
G | A | 1 | a0001c0001t0003g0167 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.71-15794C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73446564 | ||||||
| chr11:73446565
|
C | A | 1 | a0001c0001t0003g0167 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.71-15795G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73446565 | ||||||
| chr11:73447074
|
T | C | 63 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(60): Show | 63 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.71-16304A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73447074 | ||||||
| chr11:73447112
|
T | C | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.71-16342A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73447112 | ||||||
| chr11:73447245
|
C | A | 3 | a0001c0002t0001g0052a0001c0002t0020g0040a0001c0002t0020g0109 | 3 | HG01167.hp1 HG01169.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.71-16475G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73447245 | ||||||
| chr11:73447256
|
T | C | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.71-16486A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73447256 | ||||||
| chr11:73447423
|
C | T | 16 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(13): Show | 16 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.71-16653G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73447423 | ||||||
| chr11:73447557
|
CA | C | 7 | a0001c0001t0015g0132a0001c0001t0015g0133a0001c0001t0016g0135others(4): Show | 7 | HG01168.hp1 HG01261.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-16788delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73447557 | ||||||
| chr11:73447557
|
CAA | C | 19 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(16): Show | 19 | HG01884.hp1 HG02109.hp2 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.71-16789_71-16788d others(4): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73447557 | ||||||
| chr11:73447589
|
A | G | 3 | a0001c0001t0011g0148a0001c0001t0011g0149a0001c0001t0011g0150 | 3 | HG02895.hp2 HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.71-16819T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73447589 | ||||||
| chr11:73447725
|
T | C | 23 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(20): Show | 23 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.71-16955A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73447725 | ||||||
| chr11:73448043
|
T | TTTTG | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-17277_71-17274d others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73448043 | ||||||
| chr11:73448043
|
TTTTG | T | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-17277_71-17274d others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73448043 | ||||||
| chr11:73448243
|
T | C | 5 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0041g0134others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-17473A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73448243 | ||||||
| chr11:73448267
|
T | C | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.71-17497A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73448267 | ||||||
| chr11:73448465
|
G | C | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.71-17695C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73448465 | ||||||
| chr11:73448711
|
C | A | 1 | a0001c0002t0005g0110 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.71-17941G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73448711 | ||||||
| chr11:73448799
|
C | T | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.71-18029G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73448799 | ||||||
| chr11:73448827
|
T | C | 1 | a0001c0002t0001g0079 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.71-18057A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73448827 | ||||||
| chr11:73448846
|
T | A | 2 | a0001c0002t0005g0085a0002c0005t0001g0055 | 2 | HG01069.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.71-18076A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73448846 | ||||||
| chr11:73448873
|
A | T | 5 | a0001c0002t0001g0044a0001c0002t0001g0058a0001c0002t0005g0059others(2): Show | 5 | HG02083.hp2 NA18979.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-18103T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73448873 | ||||||
| chr11:73448937
|
T | C | 5 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0041g0134others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-18167A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73448937 | ||||||
| chr11:73449049
|
C | A | 1 | a0001c0004t0009g0074 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.71-18279G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73449049 | ||||||
| chr11:73449140
|
A | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.71-18370T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73449140 | ||||||
| chr11:73449260
|
G | A | 1 | a0001c0002t0001g0065 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.71-18490C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73449260 | ||||||
| chr11:73449263
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.71-18493G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73449263 | ||||||
| chr11:73449317
|
A | G | 1 | a0001c0002t0005g0155 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.71-18547T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73449317 | ||||||
| chr11:73449323
|
T | C | 1 | a0001c0002t0001g0057 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.71-18553A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73449323 | ||||||
| chr11:73449337
|
T | C | 25 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(22): Show | 25 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.71-18567A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73449337 | ||||||
| chr11:73449433
|
C | T | 3 | a0001c0001t0025g0120a0001c0001t0039g0125a0001c0001t0040g0126 | 3 | HG02055.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.71-18663G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73449433 | ||||||
| chr11:73449544
|
A | G | 55 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(52): Show | 55 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(52): Show |
intron_variant | MODIFIER | c.71-18774T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73449544 | ||||||
| chr11:73449620
|
G | C | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.70+18785C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73449620 | ||||||
| chr11:73449901
|
C | A | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+18504G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73449901 | ||||||
| chr11:73450033
|
C | G | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+18372G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73450033 | ||||||
| chr11:73450351
|
G | A | 1 | a0001c0002t0001g0036 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.70+18054C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73450351 | ||||||
| chr11:73450363
|
G | A | 2 | a0001c0002t0023g0051a0001c0002t0023g0107 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.70+18042C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73450363 | ||||||
| chr11:73450380
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.70+18025C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73450380 | ||||||
| chr11:73450637
|
C | T | 25 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(22): Show | 25 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.70+17768G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73450637 | ||||||
| chr11:73450715
|
G | A | 6 | a0001c0001t0008g0159a0001c0001t0008g0172a0001c0001t0008g0173others(3): Show | 6 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.70+17690C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73450715 | ||||||
| chr11:73450872
|
A | G | 1 | a0001c0001t0006g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.70+17533T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73450872 | ||||||
| chr11:73450894
|
A | C | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.70+17511T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73450894 | ||||||
| chr11:73450959
|
T | C | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70+17446A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73450959 | ||||||
| chr11:73451027
|
G | A | 23 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(20): Show | 23 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.70+17378C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73451027 | ||||||
| chr11:73451228
|
A | G | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+17177T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73451228 | ||||||
| chr11:73451266
|
C | A | 1 | a0001c0001t0003g0162 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.70+17139G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73451266 | ||||||
| chr11:73451566
|
A | ATTTCAGT others(8): Show |
92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.70+16838_70+16839i others(17): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73451566 | ||||||
| chr11:73451630
|
T | C | 5 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+16775A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73451630 | ||||||
| chr11:73451684
|
C | G | 23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.70+16721G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73451684 | ||||||
| chr11:73451754
|
G | A | 1 | a0001c0002t0001g0119 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.70+16651C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73451754 | ||||||
| chr11:73451896
|
G | A | 1 | a0001c0002t0001g0119 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.70+16509C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73451896 | ||||||
| chr11:73452385
|
T | C | 1 | a0001c0002t0001g0122 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.70+16020A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73452385 | ||||||
| chr11:73452386
|
T | A | 1 | a0001c0002t0001g0115 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.70+16019A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73452386 | ||||||
| chr11:73452448
|
G | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.70+15957C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73452448 | ||||||
| chr11:73452475
|
T | C | 2 | a0001c0001t0014g0153a0001c0001t0014g0154 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.70+15930A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73452475 | ||||||
| chr11:73452534
|
G | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+15871C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73452534 | ||||||
| chr11:73452803
|
C | CA | 5 | a0001c0002t0001g0087a0001c0002t0001g0098a0001c0003t0004g0063others(2): Show | 5 | HG02027.hp1 HG02109.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+15601dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73452803 | ||||||
| chr11:73452812
|
AAT | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.70+15591_70+15592d others(4): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73452812 | ||||||
| chr11:73452813
|
AT | A | 22 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(19): Show | 22 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.70+15591delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73452813 | ||||||
| chr11:73452814
|
T | A | 26 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(23): Show | 26 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.70+15591A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73452814 | ||||||
| chr11:73452817
|
T | A | 56 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(53): Show | 56 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(53): Show |
intron_variant | MODIFIER | c.70+15588A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73452817 | ||||||
| chr11:73452819
|
AT | A | 2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.70+15585delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73452819 | ||||||
| chr11:73452820
|
T | A | 53 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(50): Show | 53 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(50): Show |
intron_variant | MODIFIER | c.70+15585A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73452820 | ||||||
| chr11:73452823
|
T | A | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+15582A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73452823 | ||||||
| chr11:73452843
|
T | C | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.70+15562A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73452843 | ||||||
| chr11:73452869
|
A | G | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.70+15536T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73452869 | ||||||
| chr11:73453086
|
G | T | 2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.70+15319C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73453086 | ||||||
| chr11:73453334
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.70+15071C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73453334 | ||||||
| chr11:73453440
|
C | G | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+14965G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73453440 | ||||||
| chr11:73453446
|
AAGTTACT | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+14952_70+14958d others(9): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73453446 | ||||||
| chr11:73453668
|
T | C | 23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.70+14737A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73453668 | ||||||
| chr11:73453747
|
C | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.70+14658G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73453747 | ||||||
| chr11:73453764
|
C | T | 1 | a0001c0001t0041g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.70+14641G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73453764 | ||||||
| chr11:73453825
|
T | A | 10 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.70+14580A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73453825 | ||||||
| chr11:73454005
|
A | G | 2 | a0001c0001t0002g0007a0001c0001t0002g0018 | 2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.70+14400T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73454005 | ||||||
| chr11:73454209
|
A | G | 1 | a0001c0001t0041g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.70+14196T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73454209 | ||||||
| chr11:73454246
|
T | A | 1 | a0001c0002t0001g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.70+14159A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73454246 | ||||||
| chr11:73454284
|
T | C | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.70+14121A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73454284 | ||||||
| chr11:73454463
|
G | A | 23 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(20): Show | 23 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.70+13942C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73454463 | ||||||
| chr11:73454609
|
T | C | 1 | a0001c0001t0041g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.70+13796A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73454609 | ||||||
| chr11:73454610
|
ATC | A | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.70+13793_70+13794d others(4): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73454610 | ||||||
| chr11:73454877
|
A | C | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+13528T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73454877 | ||||||
| chr11:73455047
|
C | T | 1 | a0001c0001t0010g0002 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.70+13358G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73455047 | ||||||
| chr11:73455296
|
T | G | 1 | a0001c0002t0001g0096 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.70+13109A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73455296 | ||||||
| chr11:73455337
|
C | T | 30 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(27): Show | 30 | HG00544.hp1 HG01069.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.70+13068G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73455337 | ||||||
| chr11:73455422
|
G | A | 1 | a0001c0002t0001g0119 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.70+12983C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73455422 | ||||||
| chr11:73455649
|
C | T | 1 | a0001c0002t0005g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.70+12756G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73455649 | ||||||
| chr11:73455701
|
G | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.70+12704C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73455701 | ||||||
| chr11:73455701
|
G | C | 5 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0041g0134others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+12704C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73455701 | ||||||
| chr11:73455788
|
G | A | 23 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(20): Show | 23 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.70+12617C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73455788 | ||||||
| chr11:73455789
|
C | T | 23 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(20): Show | 23 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.70+12616G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73455789 | ||||||
| chr11:73455848
|
G | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.70+12557C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73455848 | ||||||
| chr11:73456133
|
T | C | 1 | a0001c0002t0001g0056 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.70+12272A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73456133 | ||||||
| chr11:73456270
|
C | T | 1 | a0001c0001t0037g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.70+12135G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73456270 | ||||||
| chr11:73456586
|
A | G | 1 | a0001c0002t0031g0111 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.70+11819T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73456586 | ||||||
| chr11:73456694
|
A | C | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.70+11711T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73456694 | ||||||
| chr11:73457042
|
T | C | 1 | a0001c0002t0001g0119 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.70+11363A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73457042 | ||||||
| chr11:73457184
|
T | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.70+11221A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73457184 | ||||||
| chr11:73457224
|
A | AT | 58 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(55): Show | 58 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.70+11180dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73457224 | ||||||
| chr11:73457224
|
A | T | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.70+11181T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73457224 | ||||||
| chr11:73457592
|
T | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.70+10813A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73457592 | ||||||
| chr11:73457703
|
C | T | 22 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(19): Show | 22 | HG00544.hp1 HG01069.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.70+10702G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73457703 | ||||||
| chr11:73457704
|
G | C | 8 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.70+10701C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73457704 | ||||||
| chr11:73457723
|
C | CA | 33 | a0001c0001t0003g0158a0001c0001t0003g0161a0001c0001t0003g0163others(30): Show | 33 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.70+10681dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73457723 | ||||||
| chr11:73457723
|
CA | C | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+10681delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73457723 | ||||||
| chr11:73457723
|
CAAAAAAA | C | 19 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(16): Show | 19 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.70+10675_70+10681d others(9): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73457723 | ||||||
| chr11:73457723
|
CAAAAAAA others(1): Show |
C | 22 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(19): Show | 22 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(19): Show |
intron_variant | MODIFIER | c.70+10674_70+10681d others(10): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73457723 | ||||||
| chr11:73457723
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0050g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.70+10671_70+10681d others(13): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73457723 | ||||||
| chr11:73457723
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0041g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.70+10667_70+10681d others(17): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73457723 | ||||||
| chr11:73457723
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0014g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.70+10666_70+10681d others(18): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73457723 | ||||||
| chr11:73457746
|
A | G | 18 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(15): Show | 18 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.70+10659T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73457746 | ||||||
| chr11:73457765
|
G | C | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+10640C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73457765 | ||||||
| chr11:73457770
|
G | GA | 91 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(88): Show | 91 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.70+10634dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73457770 | ||||||
| chr11:73458361
|
A | G | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.70+10044T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73458361 | ||||||
| chr11:73458401
|
C | T | 3 | a0001c0001t0025g0120a0001c0001t0039g0125a0001c0001t0040g0126 | 3 | HG02055.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.70+10004G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73458401 | ||||||
| chr11:73458428
|
C | A | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.70+9977G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73458428 | ||||||
| chr11:73458471
|
T | A | 1 | a0001c0002t0001g0098 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.70+9934A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73458471 | ||||||
| chr11:73458587
|
A | G | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.70+9818T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73458587 | ||||||
| chr11:73458617
|
C | CT | 8 | a0001c0001t0006g0024a0001c0001t0006g0067a0001c0001t0006g0180others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.70+9787dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73458617 | ||||||
| chr11:73458889
|
C | T | 1 | a0001c0001t0003g0176 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.70+9516G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73458889 | ||||||
| chr11:73459016
|
C | T | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+9389G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73459016 | ||||||
| chr11:73459027
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.70+9378C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73459027 | ||||||
| chr11:73459321
|
T | C | 1 | a0001c0002t0005g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.70+9084A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73459321 | ||||||
| chr11:73459621
|
A | G | 3 | a0001c0001t0025g0120a0001c0001t0039g0125a0001c0001t0040g0126 | 3 | HG02055.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.70+8784T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73459621 | ||||||
| chr11:73459641
|
A | G | 1 | a0001c0001t0022g0062 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.70+8764T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73459641 | ||||||
| chr11:73459879
|
A | AT | 58 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(55): Show | 58 | HG00438.hp2 HG00544.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.70+8525dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73459879 | ||||||
| chr11:73459879
|
A | ATT | 34 | a0001c0001t0002g0013a0001c0001t0002g0018a0001c0001t0004g0137others(31): Show | 34 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.70+8524_70+8525dup others(2): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73459879 | ||||||
| chr11:73460170
|
G | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.70+8235C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73460170 | ||||||
| chr11:73460212
|
G | GA | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+8192dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73460212 | ||||||
| chr11:73460261
|
T | C | 23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.70+8144A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73460261 | ||||||
| chr11:73460326
|
A | G | 1 | a0001c0001t0039g0125 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.70+8079T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73460326 | ||||||
| chr11:73460447
|
G | A | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+7958C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73460447 | ||||||
| chr11:73460465
|
A | C | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+7940T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73460465 | ||||||
| chr11:73460498
|
G | GT | 5 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(2): Show | 5 | HG02622.hp2 HG02818.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+7906_70+7907ins others(1): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73460498 | ||||||
| chr11:73460499
|
C | CT | 36 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0003g0158others(33): Show | 36 | HG00544.hp2 HG01168.hp2 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.70+7905dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73460499 | ||||||
| chr11:73460499
|
C | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+7906G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73460499 | ||||||
| chr11:73460499
|
CT | C | 18 | a0001c0001t0002g0017a0001c0001t0004g0137a0001c0001t0004g0138others(15): Show | 18 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.70+7905delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73460499 | ||||||
| chr11:73460642
|
T | C | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70+7763A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73460642 | ||||||
| chr11:73461083
|
A | C | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+7322T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73461083 | ||||||
| chr11:73461195
|
A | C | 27 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(24): Show | 27 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.70+7210T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73461195 | ||||||
| chr11:73461273
|
C | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.70+7132G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73461273 | ||||||
| chr11:73461509
|
C | T | 1 | a0001c0001t0041g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.70+6896G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73461509 | ||||||
| chr11:73461543
|
C | T | 1 | a0001c0001t0014g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.70+6862G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73461543 | ||||||
| chr11:73461581
|
G | A | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.70+6824C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73461581 | ||||||
| chr11:73461594
|
G | A | 2 | a0001c0001t0016g0135a0001c0001t0016g0136 | 2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.70+6811C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73461594 | ||||||
| chr11:73461736
|
T | C | 1 | a0001c0002t0047g0114 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.70+6669A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73461736 | ||||||
| chr11:73462136
|
A | G | 1 | a0001c0002t0050g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.70+6269T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73462136 | ||||||
| chr11:73462202
|
G | A | 1 | a0001c0002t0001g0117 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.70+6203C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73462202 | ||||||
| chr11:73462239
|
G | A | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.70+6166C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73462239 | ||||||
| chr11:73462248
|
A | G | 27 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(24): Show | 27 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.70+6157T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73462248 | ||||||
| chr11:73462451
|
A | G | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+5954T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73462451 | ||||||
| chr11:73462499
|
C | T | 27 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(24): Show | 27 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.70+5906G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73462499 | ||||||
| chr11:73462572
|
T | C | 1 | a0001c0002t0001g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.70+5833A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73462572 | ||||||
| chr11:73462604
|
G | A | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+5801C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73462604 | ||||||
| chr11:73462713
|
C | CA | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.70+5691dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73462713 | ||||||
| chr11:73462857
|
A | T | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.70+5548T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73462857 | ||||||
| chr11:73462914
|
G | GGAGAA | 23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.70+5486_70+5490dup others(5): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73462914 | ||||||
| chr11:73463023
|
C | T | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.70+5382G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73463023 | ||||||
| chr11:73463294
|
C | A | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.70+5111G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73463294 | ||||||
| chr11:73463597
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.70+4808G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73463597 | ||||||
| chr11:73463725
|
T | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.70+4680A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73463725 | ||||||
| chr11:73463900
|
C | T | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.70+4505G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73463900 | ||||||
| chr11:73464028
|
G | A | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+4377C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73464028 | ||||||
| chr11:73464092
|
T | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.70+4313A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73464092 | ||||||
| chr11:73464187
|
T | TA | 12 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(9): Show | 12 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.70+4217dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73464187 | ||||||
| chr11:73464187
|
TA | T | 17 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(14): Show | 17 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(14): Show |
intron_variant | MODIFIER | c.70+4217delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73464187 | ||||||
| chr11:73464336
|
A | G | 2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.70+4069T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73464336 | ||||||
| chr11:73464352
|
TA | T | 61 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(58): Show | 61 | HG00140.hp2 HG00544.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.70+4052delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73464352 | ||||||
| chr11:73464353
|
A | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+4052T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73464353 | ||||||
| chr11:73464354
|
A | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.70+4051T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73464354 | ||||||
| chr11:73464453
|
C | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.70+3952G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73464453 | ||||||
| chr11:73464533
|
T | A | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.70+3872A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73464533 | ||||||
| chr11:73464832
|
G | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+3573C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73464832 | ||||||
| chr11:73464864
|
C | CT | 41 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(38): Show | 41 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.70+3540_70+3541ins others(1): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73464864 | ||||||
| chr11:73464865
|
A | AT | 27 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(24): Show | 27 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.70+3539dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73464865 | ||||||
| chr11:73464865
|
A | T | 63 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(60): Show | 63 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.70+3540T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73464865 | ||||||
| chr11:73464878
|
A | T | 10 | a0001c0001t0003g0160a0001c0001t0003g0170a0001c0001t0010g0001others(7): Show | 10 | HG02109.hp2 HG02615.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.70+3527T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73464878 | ||||||
| chr11:73465077
|
A | G | 1 | a0001c0002t0001g0057 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.70+3328T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73465077 | ||||||
| chr11:73465097
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.70+3308G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73465097 | ||||||
| chr11:73465176
|
C | A | 1 | a0001c0002t0001g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.70+3229G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73465176 | ||||||
| chr11:73465272
|
G | A | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+3133C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73465272 | ||||||
| chr11:73465338
|
A | T | 1 | a0001c0002t0001g0124 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.70+3067T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73465338 | ||||||
| chr11:73465583
|
A | AGGTTCTA others(39): Show |
92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.70+2821_70+2822ins others(46): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73465583 | ||||||
| chr11:73465688
|
G | A | 1 | a0001c0001t0004g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.70+2717C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73465688 | ||||||
| chr11:73465964
|
G | GGAGA | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+2437_70+2440dup others(4): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73465964 | ||||||
| chr11:73465987
|
A | G | 1 | a0001c0001t0022g0062 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.70+2418T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73465987 | ||||||
| chr11:73466016
|
C | G | 1 | a0001c0002t0044g0049 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.70+2389G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73466016 | ||||||
| chr11:73466140
|
G | A | 12 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(9): Show | 12 | HG01106.hp2 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.70+2265C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73466140 | ||||||
| chr11:73466148
|
T | C | 3 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0043g0068 | 3 | HG01106.hp2 HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.70+2257A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73466148 | ||||||
| chr11:73466422
|
G | T | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.70+1983C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73466422 | ||||||
| chr11:73466742
|
A | G | 3 | a0001c0002t0001g0075a0001c0002t0001g0124a0001c0002t0012g0113 | 3 | HG00544.hp1 NA19056.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.70+1663T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73466742 | ||||||
| chr11:73466750
|
G | C | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.70+1655C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73466750 | ||||||
| chr11:73466794
|
G | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.70+1611C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73466794 | ||||||
| chr11:73466959
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.70+1446C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73466959 | ||||||
| chr11:73467281
|
T | G | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.70+1124A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73467281 | ||||||
| chr11:73467333
|
T | C | 1 | a0001c0002t0001g0065 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.70+1072A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73467333 | ||||||
| chr11:73467400
|
A | G | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.70+1005T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73467400 | ||||||
| chr11:73467477
|
T | C | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+928A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73467477 | ||||||
| chr11:73467558
|
T | A | 1 | a0001c0001t0041g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.70+847A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73467558 | ||||||
| chr11:73467627
|
G | C | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70+778C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73467627 | ||||||
| chr11:73467985
|
T | C | 1 | a0001c0001t0003g0176 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.70+420A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73467985 | ||||||
| chr11:73468166
|
C | G | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+239G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73468166 | ||||||
| chr11:73468176
|
G | A | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.70+229C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73468176 | ||||||
| chr11:73468191
|
A | G | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+214T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73468191 | ||||||
| chr11:73468202
|
C | T | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.70+203G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73468202 | ||||||
| chr11:73468381
|
G | A | 25 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(22): Show | 25 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.70+24C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | 73468381 | ||||||
| chr11:73468628
|
C | T | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18-136G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73468628 | ||||||
| chr11:73468673
|
G | T | 91 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(88): Show | 91 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.-18-181C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73468673 | ||||||
| chr11:73469090
|
G | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-598C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73469090 | ||||||
| chr11:73469145
|
T | G | 1 | a0001c0001t0040g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18-653A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73469145 | ||||||
| chr11:73469252
|
C | T | 5 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0025g0120others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-760G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73469252 | ||||||
| chr11:73469878
|
A | G | 2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-1386T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73469878 | ||||||
| chr11:73469934
|
C | T | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-1442G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73469934 | ||||||
| chr11:73470145
|
C | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-1653G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73470145 | ||||||
| chr11:73470202
|
G | A | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-18-1710C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73470202 | ||||||
| chr11:73470264
|
A | T | 2 | a0001c0002t0021g0054a0001c0002t0021g0104 | 2 | HG02083.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-18-1772T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73470264 | ||||||
| chr11:73470287
|
C | T | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-1795G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73470287 | ||||||
| chr11:73470424
|
C | A | 1 | a0001c0002t0001g0029 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-18-1932G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73470424 | ||||||
| chr11:73470428
|
A | G | 1 | a0001c0002t0001g0042 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-18-1936T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73470428 | ||||||
| chr11:73470488
|
A | C | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-1996T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73470488 | ||||||
| chr11:73470578
|
C | T | 49 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(46): Show | 49 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.-18-2086G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73470578 | ||||||
| chr11:73470591
|
G | A | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-2099C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73470591 | ||||||
| chr11:73471367
|
A | T | 1 | a0001c0001t0002g0015 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-18-2875T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73471367 | ||||||
| chr11:73471368
|
T | A | 2 | a0001c0002t0001g0088a0001c0002t0001g0091 | 2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-18-2876A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73471368 | ||||||
| chr11:73471648
|
T | G | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-3156A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73471648 | ||||||
| chr11:73471796
|
T | C | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-3304A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73471796 | ||||||
| chr11:73471955
|
C | A | 1 | a0001c0001t0003g0176 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-18-3463G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73471955 | ||||||
| chr11:73471999
|
C | T | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-3507G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73471999 | ||||||
| chr11:73472128
|
C | T | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18-3636G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73472128 | ||||||
| chr11:73472159
|
G | T | 30 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(27): Show | 30 | HG00544.hp1 HG01069.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-18-3667C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73472159 | ||||||
| chr11:73472254
|
G | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-3762C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73472254 | ||||||
| chr11:73472373
|
G | T | 10 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18-3881C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73472373 | ||||||
| chr11:73472611
|
G | C | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-4119C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73472611 | ||||||
| chr11:73472633
|
C | T | 1 | a0001c0002t0033g0077 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-18-4141G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73472633 | ||||||
| chr11:73472672
|
G | GTACT | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-4181_-18-4180i others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73472672 | ||||||
| chr11:73472907
|
G | A | 3 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0024g0003 | 3 | NA18965.hp1 NA18981.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-18-4415C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73472907 | ||||||
| chr11:73472957
|
C | T | 62 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 62 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(59): Show |
intron_variant | MODIFIER | c.-18-4465G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73472957 | ||||||
| chr11:73472970
|
CCATTAGG others(4): Show |
C | 1 | a0001c0001t0003g0176 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-18-4489_-18-4479d others(13): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73472970 | ||||||
| chr11:73473325
|
A | G | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-4833T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73473325 | ||||||
| chr11:73473364
|
A | G | 1 | a0001c0001t0003g0166 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-18-4872T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73473364 | ||||||
| chr11:73473389
|
A | G | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-4897T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73473389 | ||||||
| chr11:73473530
|
T | C | 1 | a0001c0002t0009g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-18-5038A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73473530 | ||||||
| chr11:73473653
|
C | G | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-5161G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73473653 | ||||||
| chr11:73473818
|
C | A | 1 | a0001c0001t0041g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-18-5326G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73473818 | ||||||
| chr11:73474243
|
C | T | 25 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(22): Show | 25 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18-5751G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73474243 | ||||||
| chr11:73474273
|
C | T | 1 | a0001c0002t0001g0065 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-18-5781G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73474273 | ||||||
| chr11:73474304
|
T | G | 12 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(9): Show | 12 | HG01884.hp1 HG02717.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.-18-5812A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73474304 | ||||||
| chr11:73474329
|
AT | A | 59 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(56): Show | 59 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.-18-5838delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73474329 | ||||||
| chr11:73474347
|
T | G | 178 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-18-5855A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73474347 | ||||||
| chr11:73474406
|
C | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-5914G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73474406 | ||||||
| chr11:73474520
|
C | T | 2 | a0001c0002t0023g0051a0001c0002t0023g0107 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-18-6028G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73474520 | ||||||
| chr11:73474822
|
T | C | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-6330A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73474822 | ||||||
| chr11:73475142
|
T | C | 1 | a0001c0002t0031g0111 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-18-6650A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73475142 | ||||||
| chr11:73475192
|
C | T | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-6700G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73475192 | ||||||
| chr11:73475205
|
T | C | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-6713A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73475205 | ||||||
| chr11:73475304
|
CA | C | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-6813delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73475304 | ||||||
| chr11:73475493
|
C | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-7001G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73475493 | ||||||
| chr11:73475575
|
C | T | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-7083G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73475575 | ||||||
| chr11:73475640
|
T | TA | 32 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(29): Show | 32 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.-18-7149dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73475640 | ||||||
| chr11:73475640
|
T | TAA | 9 | a0001c0001t0003g0171a0001c0001t0004g0137a0001c0001t0004g0138others(6): Show | 9 | HG01884.hp1 HG02572.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18-7150_-18-7149d others(4): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73475640 | ||||||
| chr11:73475712
|
A | T | 1 | a0001c0001t0006g0180 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-18-7220T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73475712 | ||||||
| chr11:73475724
|
T | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18-7232A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73475724 | ||||||
| chr11:73475819
|
A | T | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-18-7327T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73475819 | ||||||
| chr11:73476070
|
T | C | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-7578A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73476070 | ||||||
| chr11:73476124
|
T | C | 2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-18-7632A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73476124 | ||||||
| chr11:73476238
|
G | A | 7 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(4): Show | 7 | HG01255.hp1 HG01257.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18-7746C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73476238 | ||||||
| chr11:73476282
|
A | G | 3 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139 | 3 | HG01884.hp1 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-18-7790T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73476282 | ||||||
| chr11:73476432
|
A | G | 1 | a0001c0001t0041g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-18-7940T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73476432 | ||||||
| chr11:73476452
|
G | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-7960C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73476452 | ||||||
| chr11:73476490
|
G | T | 2 | a0001c0001t0011g0149a0001c0001t0011g0150 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-18-7998C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73476490 | ||||||
| chr11:73476689
|
C | A | 1 | a0001c0002t0001g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-18-8197G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73476689 | ||||||
| chr11:73476817
|
G | A | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-8325C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73476817 | ||||||
| chr11:73477216
|
G | T | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-18-8724C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477216 | ||||||
| chr11:73477315
|
G | C | 40 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(37): Show | 40 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.-18-8823C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477315 | ||||||
| chr11:73477332
|
C | T | 1 | a0001c0002t0021g0054 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-18-8840G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477332 | ||||||
| chr11:73477603
|
C | T | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-9111G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477603 | ||||||
| chr11:73477696
|
C | CA | 35 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(32): Show | 35 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.-18-9205dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477696 | ||||||
| chr11:73477704
|
C | G | 1 | a0001c0002t0049g0072 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-18-9212G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477704 | ||||||
| chr11:73477759
|
A | T | 1 | a0001c0001t0003g0168 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-18-9267T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477759 | ||||||
| chr11:73477888
|
C | T | 4 | a0001c0002t0001g0071a0001c0002t0001g0121a0001c0002t0001g0122others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-9396G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477888 | ||||||
| chr11:73477921
|
G | GTAGATAG others(5): Show |
1 | a0001c0001t0016g0136 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-18-9441_-18-9430d others(14): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477921 | ||||||
| chr11:73477921
|
GTAGA | G | 65 | a0001c0001t0003g0158a0001c0001t0006g0020a0001c0001t0006g0021others(62): Show | 65 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.-18-9433_-18-9430d others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477921 | ||||||
| chr11:73477921
|
GTAGATAG others(1): Show |
G | 27 | a0001c0001t0002g0013a0001c0001t0002g0017a0001c0001t0002g0019others(24): Show | 27 | HG00323.hp1 HG01106.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-18-9437_-18-9430d others(10): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477921 | ||||||
| chr11:73477921
|
GTAGATAG others(5): Show |
G | 23 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0008others(20): Show | 23 | HG00438.hp1 HG01168.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-9441_-18-9430d others(14): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477921 | ||||||
| chr11:73477921
|
GTAGATAG others(9): Show |
G | 7 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0003g0162others(4): Show | 7 | HG00544.hp2 HG01978.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18-9445_-18-9430d others(18): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477921 | ||||||
| chr11:73477922
|
T | TAGAC | 5 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0022g0061others(2): Show | 5 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-9431_-18-9430i others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477922 | ||||||
| chr11:73477962
|
T | TAGAC | 11 | a0001c0001t0004g0137a0001c0001t0004g0139a0001c0001t0004g0140others(8): Show | 11 | HG01884.hp1 HG02258.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-9471_-18-9470i others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477962 | ||||||
| chr11:73477962
|
T | TAGATAGA others(1): Show |
13 | a0001c0001t0004g0138a0001c0001t0004g0145a0001c0001t0004g0147others(10): Show | 13 | HG01106.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-18-9471_-18-9470i others(10): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477962 | ||||||
| chr11:73477962
|
T | TAGATAGA others(5): Show |
3 | a0001c0001t0004g0142a0001c0001t0004g0143a0001c0001t0042g0060 | 3 | HG02572.hp2 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-18-9471_-18-9470i others(14): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477962 | ||||||
| chr11:73477966
|
T | G | 1 | a0001c0002t0005g0059 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-18-9474A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477966 | ||||||
| chr11:73477987
|
A | G | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-9495T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73477987 | ||||||
| chr11:73478120
|
C | T | 121 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(118): Show | 121 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.-18-9628G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73478120 | ||||||
| chr11:73478196
|
A | G | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-9704T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73478196 | ||||||
| chr11:73478272
|
G | A | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18-9780C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73478272 | ||||||
| chr11:73478517
|
A | ATTTT | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-10026_-18-1002 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73478517 | ||||||
| chr11:73478520
|
T | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-10028A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73478520 | ||||||
| chr11:73478522
|
TA | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-10031delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73478522 | ||||||
| chr11:73478568
|
A | G | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-18-10076T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73478568 | ||||||
| chr11:73478677
|
A | G | 1 | a0001c0001t0041g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-18-10185T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73478677 | ||||||
| chr11:73478726
|
C | G | 1 | a0001c0002t0033g0077 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-18-10234G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73478726 | ||||||
| chr11:73478970
|
A | G | 1 | a0001c0002t0033g0077 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-18-10478T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73478970 | ||||||
| chr11:73479103
|
C | T | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-10611G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73479103 | ||||||
| chr11:73479131
|
T | C | 1 | a0001c0002t0001g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-18-10639A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73479131 | ||||||
| chr11:73479307
|
C | T | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-10815G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73479307 | ||||||
| chr11:73479401
|
CTA | C | 41 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(38): Show | 41 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.-18-10911_-18-1091 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73479401 | ||||||
| chr11:73479523
|
T | C | 1 | a0001c0002t0001g0031 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-18-11031A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73479523 | ||||||
| chr11:73479652
|
A | G | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-11160T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73479652 | ||||||
| chr11:73479913
|
C | T | 15 | a0001c0002t0001g0053a0001c0002t0001g0094a0001c0002t0001g0106others(12): Show | 15 | HG00140.hp1 HG00323.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18-11421G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73479913 | ||||||
| chr11:73479948
|
G | A | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18-11456C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73479948 | ||||||
| chr11:73480020
|
T | A | 1 | a0001c0002t0005g0059 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-18-11528A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73480020 | ||||||
| chr11:73480384
|
TTCTC | T | 41 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(38): Show | 41 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.-18-11896_-18-1189 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73480384 | ||||||
| chr11:73480535
|
T | C | 1 | a0001c0001t0006g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-18-12043A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73480535 | ||||||
| chr11:73480638
|
C | T | 2 | a0001c0001t0003g0160a0001c0001t0003g0170 | 2 | NA19005.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.-18-12146G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73480638 | ||||||
| chr11:73480664
|
G | A | 123 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(120): Show | 123 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-18-12172C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73480664 | ||||||
| chr11:73480684
|
C | T | 1 | a0001c0002t0021g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-18-12192G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73480684 | ||||||
| chr11:73480699
|
AAAAC | A | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02258.hp2 HG02451.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-12211_-18-1220 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73480699 | ||||||
| chr11:73480720
|
AAAC | A | 27 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(24): Show | 27 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18-12231_-18-1222 others(7): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73480720 | ||||||
| chr11:73480808
|
C | G | 2 | a0001c0001t0017g0032a0001c0001t0017g0078 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-18-12316G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73480808 | ||||||
| chr11:73481041
|
C | A | 90 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(87): Show | 90 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.-18-12549G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73481041 | ||||||
| chr11:73481073
|
CAGTCTGG | C | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-12588_-18-1258 others(11): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73481073 | ||||||
| chr11:73481194
|
C | T | 1 | a0001c0002t0012g0082 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-18-12702G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73481194 | ||||||
| chr11:73481201
|
G | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-12709C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73481201 | ||||||
| chr11:73481201
|
G | T | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-18-12709C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73481201 | ||||||
| chr11:73481366
|
C | T | 1 | a0001c0002t0001g0119 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-18-12874G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73481366 | ||||||
| chr11:73481458
|
T | A | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18-12966A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73481458 | ||||||
| chr11:73481770
|
C | T | 1 | a0001c0002t0001g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-18-13278G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73481770 | ||||||
| chr11:73481881
|
C | T | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-13389G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73481881 | ||||||
| chr11:73482001
|
G | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-13509C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73482001 | ||||||
| chr11:73482054
|
C | T | 1 | a0001c0002t0001g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-18-13562G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73482054 | ||||||
| chr11:73482162
|
A | G | 5 | a0001c0001t0003g0160a0001c0001t0003g0163a0001c0001t0003g0164others(2): Show | 5 | NA18977.hp1 NA18983.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18-13670T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73482162 | ||||||
| chr11:73482181
|
C | CT | 63 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(60): Show | 63 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.-18-13690dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73482181 | ||||||
| chr11:73482181
|
C | CTT | 25 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(22): Show | 25 | HG00544.hp2 HG01069.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18-13691_-18-1369 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73482181 | ||||||
| chr11:73482181
|
CT | C | 24 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(21): Show | 24 | HG01069.hp1 HG01106.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.-18-13690delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73482181 | ||||||
| chr11:73482181
|
CTT | C | 17 | a0001c0001t0004g0142a0001c0001t0004g0147a0001c0001t0004g0151others(14): Show | 17 | HG02055.hp1 HG02258.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.-18-13691_-18-1369 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73482181 | ||||||
| chr11:73482320
|
TGGA | T | 23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-13831_-18-1382 others(7): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73482320 | ||||||
| chr11:73482393
|
G | A | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-13901C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73482393 | ||||||
| chr11:73482769
|
C | G | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-14277G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73482769 | ||||||
| chr11:73482788
|
G | A | 1 | a0001c0002t0001g0056 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-18-14296C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73482788 | ||||||
| chr11:73482841
|
C | T | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18-14349G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73482841 | ||||||
| chr11:73482857
|
G | A | 1 | a0001c0001t0011g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-18-14365C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73482857 | ||||||
| chr11:73483004
|
T | A | 2 | a0001c0002t0001g0075a0001c0002t0001g0124 | 2 | HG00544.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-18-14512A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73483004 | ||||||
| chr11:73483120
|
T | G | 1 | a0001c0002t0001g0056 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-18-14628A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73483120 | ||||||
| chr11:73483343
|
A | G | 5 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0025g0120others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-14851T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73483343 | ||||||
| chr11:73483600
|
A | G | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(89): Show |
intron_variant | MODIFIER | c.-18-15108T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73483600 | ||||||
| chr11:73483626
|
C | T | 6 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(3): Show | 6 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-15134G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73483626 | ||||||
| chr11:73483660
|
G | A | 1 | a0001c0002t0045g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-18-15168C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73483660 | ||||||
| chr11:73483675
|
A | G | 1 | a0001c0002t0049g0072 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-18-15183T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73483675 | ||||||
| chr11:73483849
|
C | T | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18-15357G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73483849 | ||||||
| chr11:73483951
|
C | A | 1 | a0001c0002t0001g0115 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-18-15459G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73483951 | ||||||
| chr11:73483961
|
T | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18-15469A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73483961 | ||||||
| chr11:73484184
|
T | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-15692A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484184 | ||||||
| chr11:73484204
|
A | G | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18-15712T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484204 | ||||||
| chr11:73484207
|
T | C | 3 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0043g0068 | 3 | HG01106.hp2 HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-18-15715A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484207 | ||||||
| chr11:73484505
|
GAGATATA others(7): Show |
G | 22 | a0001c0001t0004g0137a0001c0001t0004g0139a0001c0001t0004g0140others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-18-16027_-18-1601 others(18): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484505 | ||||||
| chr11:73484507
|
G | GAGAGATA others(19): Show |
1 | a0001c0002t0001g0079 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-18-16016_-18-1601 others(30): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484507 | ||||||
| chr11:73484509
|
T | G | 63 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(60): Show | 63 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.-18-16017A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484509 | ||||||
| chr11:73484510
|
A | C | 1 | a0001c0002t0001g0079 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-18-16018T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484510 | ||||||
| chr11:73484511
|
T | G | 63 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(60): Show | 63 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.-18-16019A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484511 | ||||||
| chr11:73484511
|
TATATAG | T | 2 | a0001c0001t0025g0120a0001c0001t0042g0060 | 2 | NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-18-16025_-18-1602 others(10): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484511 | ||||||
| chr11:73484513
|
T | G | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-16021A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484513 | ||||||
| chr11:73484515
|
T | G | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-16023A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484515 | ||||||
| chr11:73484517
|
G | T | 66 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(63): Show | 66 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.-18-16025C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484517 | ||||||
| chr11:73484518
|
A | C | 1 | a0001c0002t0001g0079 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-18-16026T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484518 | ||||||
| chr11:73484519
|
T | G | 1 | a0001c0001t0040g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18-16027A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484519 | ||||||
| chr11:73484520
|
A | ATC | 3 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0043g0068 | 3 | HG01106.hp2 HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-18-16029_-18-1602 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484520 | ||||||
| chr11:73484522
|
A | C | 41 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(38): Show | 41 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.-18-16030T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484522 | ||||||
| chr11:73484528
|
C | A | 24 | a0001c0001t0004g0137a0001c0001t0004g0139a0001c0001t0004g0140others(21): Show | 24 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-18-16036G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484528 | ||||||
| chr11:73484530
|
A | ATC | 3 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0043g0068 | 3 | HG01106.hp2 HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-18-16039_-18-1603 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484530 | ||||||
| chr11:73484536
|
C | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-16044G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484536 | ||||||
| chr11:73484540
|
A | C | 4 | a0001c0001t0004g0138a0001c0001t0024g0003a0001c0001t0025g0120others(1): Show | 4 | HG03130.hp1 NA18965.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-16048T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484540 | ||||||
| chr11:73484544
|
C | A | 6 | a0001c0001t0004g0138a0001c0001t0024g0003a0001c0001t0025g0120others(3): Show | 6 | HG02055.hp2 HG02647.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-16052G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484544 | ||||||
| chr11:73484546
|
A | C | 4 | a0001c0001t0004g0138a0001c0001t0024g0003a0001c0001t0025g0120others(1): Show | 4 | HG03130.hp1 NA18965.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-16054T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484546 | ||||||
| chr11:73484546
|
ATC | A | 3 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0043g0068 | 3 | HG01106.hp2 HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-18-16056_-18-1605 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484546 | ||||||
| chr11:73484548
|
C | A | 5 | a0001c0001t0004g0138a0001c0001t0024g0003a0001c0001t0025g0120others(2): Show | 5 | HG02055.hp2 HG03130.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-16056G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484548 | ||||||
| chr11:73484548
|
C | CTATATCT others(1): Show |
26 | a0001c0001t0004g0137a0001c0001t0004g0139a0001c0001t0004g0140others(23): Show | 26 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18-16064_-18-1605 others(12): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484548 | ||||||
| chr11:73484548
|
C | CTATATCT others(9): Show |
23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-16072_-18-1605 others(20): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484548 | ||||||
| chr11:73484548
|
C | CTATATCT others(35): Show |
4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-16057_-18-1605 others(46): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484548 | ||||||
| chr11:73484548
|
C | CTATATCT others(27): Show |
40 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(37): Show | 40 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.-18-16057_-18-1605 others(38): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484548 | ||||||
| chr11:73484572
|
A | ATATATCT others(39): Show |
1 | a0001c0001t0004g0145 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-18-16081_-18-1608 others(50): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484572 | ||||||
| chr11:73484579
|
G | T | 3 | a0001c0001t0011g0148a0001c0001t0011g0149a0001c0001t0011g0150 | 3 | HG02895.hp2 HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18-16087C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484579 | ||||||
| chr11:73484583
|
T | TATCG | 3 | a0001c0001t0011g0148a0001c0001t0011g0149a0001c0001t0011g0150 | 3 | HG02895.hp2 HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18-16092_-18-1609 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484583 | ||||||
| chr11:73484584
|
C | A | 3 | a0001c0001t0011g0148a0001c0001t0011g0149a0001c0001t0011g0150 | 3 | HG02895.hp2 HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18-16092G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484584 | ||||||
| chr11:73484602
|
C | CTA | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-16112_-18-1611 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484602 | ||||||
| chr11:73484614
|
A | C | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-16122T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484614 | ||||||
| chr11:73484624
|
A | C | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-16132T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484624 | ||||||
| chr11:73484626
|
A | C | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-16134T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484626 | ||||||
| chr11:73484635
|
T | C | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18-16143A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484635 | ||||||
| chr11:73484640
|
ATATC | A | 32 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(29): Show | 32 | HG01884.hp1 HG02258.hp2 HG02451.hp2 others(29): Show |
intron_variant | MODIFIER | c.-18-16152_-18-1614 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484640 | ||||||
| chr11:73484676
|
G | A | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(89): Show |
intron_variant | MODIFIER | c.-18-16184C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484676 | ||||||
| chr11:73484682
|
CTATAGAT others(7): Show |
C | 1 | a0002c0005t0001g0055 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-18-16204_-18-1619 others(18): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484682 | ||||||
| chr11:73484691
|
TATAG | T | 40 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(37): Show | 40 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.-18-16203_-18-1620 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484691 | ||||||
| chr11:73484692
|
A | C | 29 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(26): Show | 29 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-18-16200T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484692 | ||||||
| chr11:73484701
|
GATATATA others(5): Show |
G | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-16221_-18-1621 others(16): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484701 | ||||||
| chr11:73484713
|
TATATATA others(13): Show |
T | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18-16241_-18-1622 others(24): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484713 | ||||||
| chr11:73484732
|
CGATATAT others(1): Show |
C | 3 | a0001c0001t0011g0148a0001c0001t0011g0149a0001c0001t0011g0150 | 3 | HG02895.hp2 HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-18-16248_-18-1624 others(12): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484732 | ||||||
| chr11:73484740
|
A | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18-16248T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73484740 | ||||||
| chr11:73485330
|
A | G | 2 | a0001c0002t0023g0051a0001c0002t0023g0107 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-18-16838T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73485330 | ||||||
| chr11:73485383
|
T | C | 49 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(46): Show | 49 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.-18-16891A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73485383 | ||||||
| chr11:73485830
|
GCTA | G | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-17341_-18-1733 others(7): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73485830 | ||||||
| chr11:73486023
|
T | C | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18-17531A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73486023 | ||||||
| chr11:73486086
|
C | T | 1 | a0001c0002t0001g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-18-17594G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73486086 | ||||||
| chr11:73486111
|
G | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-17619C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73486111 | ||||||
| chr11:73486163
|
C | A | 122 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(119): Show | 122 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.-18-17671G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73486163 | ||||||
| chr11:73486271
|
T | C | 1 | a0001c0002t0005g0085 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-18-17779A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73486271 | ||||||
| chr11:73486449
|
A | G | 1 | a0001c0001t0026g0144 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-18-17957T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73486449 | ||||||
| chr11:73486491
|
A | G | 1 | a0001c0001t0052g0157 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-18-17999T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73486491 | ||||||
| chr11:73486581
|
C | G | 1 | a0001c0002t0001g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-18-18089G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73486581 | ||||||
| chr11:73486657
|
T | C | 1 | a0001c0002t0050g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-18-18165A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73486657 | ||||||
| chr11:73487001
|
A | C | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-18509T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73487001 | ||||||
| chr11:73487040
|
T | C | 1 | a0001c0002t0001g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-18-18548A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73487040 | ||||||
| chr11:73487042
|
A | G | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-18550T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73487042 | ||||||
| chr11:73487067
|
A | G | 2 | a0001c0001t0014g0153a0001c0001t0014g0154 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-18-18575T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73487067 | ||||||
| chr11:73487095
|
T | C | 1 | a0001c0002t0005g0048 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-18-18603A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73487095 | ||||||
| chr11:73487151
|
A | G | 1 | a0001c0002t0001g0086 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-18-18659T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73487151 | ||||||
| chr11:73487376
|
T | C | 1 | a0001c0002t0001g0079 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-18-18884A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73487376 | ||||||
| chr11:73487379
|
C | A | 1 | a0001c0002t0033g0077 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-18-18887G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73487379 | ||||||
| chr11:73487449
|
T | G | 41 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(38): Show | 41 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.-18-18957A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73487449 | ||||||
| chr11:73487457
|
C | T | 1 | a0001c0002t0001g0056 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-18-18965G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73487457 | ||||||
| chr11:73487541
|
T | G | 1 | a0001c0002t0005g0110 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-18-19049A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73487541 | ||||||
| chr11:73487639
|
C | T | 2 | a0001c0001t0016g0135a0001c0001t0016g0136 | 2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-18-19147G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73487639 | ||||||
| chr11:73487699
|
G | C | 27 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(24): Show | 27 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18-19207C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73487699 | ||||||
| chr11:73488016
|
C | T | 1 | a0001c0002t0031g0111 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-18-19524G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73488016 | ||||||
| chr11:73488018
|
G | A | 90 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(87): Show | 90 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.-18-19526C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73488018 | ||||||
| chr11:73488128
|
G | T | 179 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-18-19636C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73488128 | ||||||
| chr11:73488130
|
C | T | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-19638G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73488130 | ||||||
| chr11:73488140
|
T | TC | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-19649_-18-1964 others(5): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73488140 | ||||||
| chr11:73488281
|
C | A | 8 | a0001c0001t0004g0142a0001c0001t0004g0147a0001c0001t0004g0151others(5): Show | 8 | HG02717.hp1 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18-19789G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73488281 | ||||||
| chr11:73488540
|
C | T | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-18-20048G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73488540 | ||||||
| chr11:73488877
|
A | G | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-20385T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73488877 | ||||||
| chr11:73488951
|
C | T | 41 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(38): Show | 41 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.-18-20459G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73488951 | ||||||
| chr11:73488958
|
A | G | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-20466T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73488958 | ||||||
| chr11:73488993
|
A | G | 41 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(38): Show | 41 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.-18-20501T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73488993 | ||||||
| chr11:73489021
|
T | C | 1 | a0001c0002t0033g0077 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-18-20529A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73489021 | ||||||
| chr11:73489353
|
C | T | 3 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0028 | 3 | HG02451.hp1 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-18-20861G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73489353 | ||||||
| chr11:73489407
|
T | C | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-20915A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73489407 | ||||||
| chr11:73489510
|
C | CT | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-21019dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73489510 | ||||||
| chr11:73489510
|
C | CTT | 10 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(7): Show | 10 | HG01106.hp2 HG01884.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18-21020_-18-2101 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73489510 | ||||||
| chr11:73489613
|
C | T | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18-21121G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73489613 | ||||||
| chr11:73489614
|
G | A | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18-21122C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73489614 | ||||||
| chr11:73490298
|
CT | C | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-21807delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73490298 | ||||||
| chr11:73490662
|
A | G | 23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-22170T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73490662 | ||||||
| chr11:73490781
|
C | T | 41 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(38): Show | 41 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.-18-22289G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73490781 | ||||||
| chr11:73490846
|
C | A | 2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-22354G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73490846 | ||||||
| chr11:73490871
|
G | A | 41 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(38): Show | 41 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.-18-22379C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73490871 | ||||||
| chr11:73490944
|
A | G | 1 | a0001c0001t0041g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-18-22452T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73490944 | ||||||
| chr11:73491496
|
T | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18-23004A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73491496 | ||||||
| chr11:73491592
|
C | G | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-23100G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73491592 | ||||||
| chr11:73491610
|
T | C | 1 | a0001c0002t0001g0053 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-18-23118A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73491610 | ||||||
| chr11:73492355
|
A | C | 2 | a0001c0001t0010g0001a0001c0001t0010g0002 | 2 | NA18981.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-18-23863T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73492355 | ||||||
| chr11:73492384
|
T | C | 2 | a0001c0002t0001g0065a0001c0002t0001g0066 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-18-23892A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73492384 | ||||||
| chr11:73492543
|
G | A | 1 | a0001c0002t0021g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-18-24051C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73492543 | ||||||
| chr11:73492569
|
A | T | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-24077T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73492569 | ||||||
| chr11:73492625
|
G | A | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-24133C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73492625 | ||||||
| chr11:73492742
|
G | A | 23 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(20): Show | 23 | HG02055.hp2 HG02451.hp2 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-24250C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73492742 | ||||||
| chr11:73492829
|
G | A | 23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-24337C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73492829 | ||||||
| chr11:73492977
|
G | A | 1 | a0001c0002t0050g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-18-24485C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73492977 | ||||||
| chr11:73493035
|
G | C | 2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-18-24543C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73493035 | ||||||
| chr11:73493536
|
C | G | 2 | a0001c0002t0001g0075a0001c0002t0001g0124 | 2 | HG00544.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-18-25044G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73493536 | ||||||
| chr11:73493561
|
G | A | 3 | a0001c0001t0004g0142a0001c0001t0004g0147a0001c0001t0027g0146 | 3 | HG02717.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-18-25069C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73493561 | ||||||
| chr11:73493574
|
C | T | 10 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18-25082G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73493574 | ||||||
| chr11:73493657
|
T | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-25165A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73493657 | ||||||
| chr11:73493694
|
G | A | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-25202C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73493694 | ||||||
| chr11:73493698
|
T | G | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-18-25206A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73493698 | ||||||
| chr11:73493742
|
A | T | 2 | a0001c0001t0007g0022a0001c0001t0007g0023 | 2 | HG01167.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-18-25250T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73493742 | ||||||
| chr11:73493911
|
C | T | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-25419G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73493911 | ||||||
| chr11:73494135
|
T | G | 5 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-25643A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73494135 | ||||||
| chr11:73494587
|
G | A | 122 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(119): Show | 122 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.-18-26095C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73494587 | ||||||
| chr11:73494732
|
A | G | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-26240T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73494732 | ||||||
| chr11:73494821
|
G | A | 5 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0025g0120others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-26329C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73494821 | ||||||
| chr11:73494925
|
C | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-26433G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73494925 | ||||||
| chr11:73494934
|
C | G | 4 | a0001c0002t0001g0071a0001c0002t0001g0121a0001c0002t0001g0122others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-26442G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73494934 | ||||||
| chr11:73494937
|
A | G | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-26445T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73494937 | ||||||
| chr11:73494964
|
C | T | 2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-18-26472G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73494964 | ||||||
| chr11:73495003
|
C | CA | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-26512dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73495003 | ||||||
| chr11:73495092
|
T | C | 1 | a0001c0002t0001g0029 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-18-26600A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73495092 | ||||||
| chr11:73495094
|
G | C | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-18-26602C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73495094 | ||||||
| chr11:73495127
|
T | TA | 43 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(40): Show | 43 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.-18-26636dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73495127 | ||||||
| chr11:73495307
|
C | T | 4 | a0001c0001t0004g0143a0001c0001t0004g0145a0001c0001t0026g0144others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-26815G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73495307 | ||||||
| chr11:73495309
|
A | G | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-26817T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73495309 | ||||||
| chr11:73495609
|
T | C | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-18-27117A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73495609 | ||||||
| chr11:73495684
|
C | T | 63 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(60): Show | 63 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.-18-27192G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73495684 | ||||||
| chr11:73496072
|
TGCATACA others(8): Show |
T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-27595_-18-2758 others(19): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496072 | ||||||
| chr11:73496114
|
C | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-27622G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496114 | ||||||
| chr11:73496115
|
G | A | 25 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(22): Show | 25 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18-27623C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496115 | ||||||
| chr11:73496354
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-18-27862C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496354 | ||||||
| chr11:73496472
|
T | C | 60 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(57): Show | 60 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.-18-27980A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496472 | ||||||
| chr11:73496556
|
T | G | 3 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0091 | 3 | HG02622.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-18-28064A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496556 | ||||||
| chr11:73496560
|
G | T | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18-28068C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496560 | ||||||
| chr11:73496610
|
G | A | 2 | a0001c0001t0016g0135a0001c0001t0016g0136 | 2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-18-28118C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496610 | ||||||
| chr11:73496661
|
C | G | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-28169G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496661 | ||||||
| chr11:73496691
|
G | T | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-28199C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496691 | ||||||
| chr11:73496775
|
T | C | 2 | a0001c0002t0001g0058a0001c0002t0005g0059 | 2 | NA18981.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-18-28283A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496775 | ||||||
| chr11:73496873
|
T | TCA | 28 | a0001c0001t0003g0160a0001c0001t0003g0162a0001c0001t0003g0163others(25): Show | 28 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-28383_-18-2838 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496873 | ||||||
| chr11:73496873
|
T | TCACA | 6 | a0001c0001t0003g0158a0001c0001t0003g0176a0001c0001t0016g0135others(3): Show | 6 | HG02083.hp1 HG03130.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-28385_-18-2838 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496873 | ||||||
| chr11:73496873
|
T | TCACACAC others(1): Show |
4 | a0001c0001t0004g0142a0001c0001t0004g0151a0001c0001t0025g0120others(1): Show | 4 | HG02717.hp1 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-28389_-18-2838 others(12): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496873 | ||||||
| chr11:73496873
|
T | TCACACAC others(3): Show |
3 | a0001c0001t0004g0138a0001c0001t0004g0139a0001c0001t0004g0140 | 3 | HG01884.hp1 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-18-28391_-18-2838 others(14): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496873 | ||||||
| chr11:73496873
|
T | TCACACAC others(5): Show |
9 | a0001c0001t0002g0005a0001c0001t0002g0015a0001c0001t0004g0137others(6): Show | 9 | HG02572.hp2 HG02717.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18-28393_-18-2838 others(16): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496873 | ||||||
| chr11:73496873
|
T | TCACACAC others(9): Show |
3 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0009 | 3 | HG02922.hp1 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-18-28397_-18-2838 others(20): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496873 | ||||||
| chr11:73496873
|
T | TCACACAC others(11): Show |
4 | a0001c0001t0002g0010a0001c0001t0002g0013a0001c0001t0011g0149others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-28399_-18-2838 others(22): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496873 | ||||||
| chr11:73496873
|
T | TCACACAC others(13): Show |
2 | a0001c0001t0002g0014a0001c0001t0002g0019 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18-28401_-18-2838 others(24): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496873 | ||||||
| chr11:73496873
|
T | TCACACAC others(15): Show |
6 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0016others(3): Show | 6 | HG02451.hp2 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-28403_-18-2838 others(26): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496873 | ||||||
| chr11:73496873
|
T | TCACACAC others(17): Show |
1 | a0001c0001t0002g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-18-28405_-18-2838 others(28): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496873 | ||||||
| chr11:73496873
|
T | TCTCA | 3 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0022g0061 | 3 | HG02818.hp2 NA18981.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-18-28382_-18-2838 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496873 | ||||||
| chr11:73496873
|
T | TCTCACAC others(1): Show |
2 | a0001c0001t0010g0004a0001c0001t0024g0003 | 2 | NA18965.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-18-28382_-18-2838 others(12): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496873 | ||||||
| chr11:73496873
|
TCA | T | 18 | a0001c0001t0006g0067a0001c0001t0014g0153a0001c0001t0014g0154others(15): Show | 18 | HG01106.hp2 HG01109.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-18-28383_-18-2838 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496873 | ||||||
| chr11:73496873
|
TCACA | T | 5 | a0001c0001t0015g0132a0001c0001t0015g0133a0001c0002t0009g0073others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18-28385_-18-2838 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496873 | ||||||
| chr11:73496890
|
C | CACAA | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-28399_-18-2839 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496890 | ||||||
| chr11:73496897
|
A | G | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-28405T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496897 | ||||||
| chr11:73496903
|
A | ACACG | 9 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0028others(6): Show | 9 | HG01167.hp2 HG01255.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18-28415_-18-2841 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496903 | ||||||
| chr11:73496905
|
A | ACACACAC others(7): Show |
1 | a0001c0003t0004g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18-28414_-18-2841 others(18): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496905 | ||||||
| chr11:73496905
|
A | ACACACAC others(5): Show |
1 | a0001c0003t0028g0064 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-18-28414_-18-2841 others(16): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496905 | ||||||
| chr11:73496907
|
G | A | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-18-28415C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496907 | ||||||
| chr11:73496911
|
A | G | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18-28419T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496911 | ||||||
| chr11:73496915
|
ACG | A | 3 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128 | 3 | HG02055.hp1 HG02559.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-18-28425_-18-2842 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496915 | ||||||
| chr11:73496917
|
G | A | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18-28425C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496917 | ||||||
| chr11:73496921
|
A | G | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18-28429T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73496921 | ||||||
| chr11:73497012
|
A | G | 1 | a0001c0001t0037g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-18-28520T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73497012 | ||||||
| chr11:73497334
|
G | A | 1 | a0001c0002t0001g0098 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-18-28842C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73497334 | ||||||
| chr11:73497401
|
G | C | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-28909C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73497401 | ||||||
| chr11:73497591
|
C | G | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-29099G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73497591 | ||||||
| chr11:73497672
|
C | T | 1 | a0001c0002t0001g0089 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-29180G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73497672 | ||||||
| chr11:73497701
|
A | G | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18-29209T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73497701 | ||||||
| chr11:73497866
|
C | T | 10 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18-29374G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73497866 | ||||||
| chr11:73497943
|
C | G | 1 | a0001c0001t0004g0145 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-18-29451G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73497943 | ||||||
| chr11:73498324
|
C | A | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-18-29832G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73498324 | ||||||
| chr11:73498590
|
G | C | 1 | a0001c0002t0001g0086 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-18-30098C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73498590 | ||||||
| chr11:73498609
|
A | G | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18-30117T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73498609 | ||||||
| chr11:73498687
|
G | A | 1 | a0001c0002t0001g0099 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-18-30195C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73498687 | ||||||
| chr11:73498873
|
C | T | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18-30381G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73498873 | ||||||
| chr11:73498892
|
C | T | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-30400G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73498892 | ||||||
| chr11:73499047
|
C | T | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-30555G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73499047 | ||||||
| chr11:73499134
|
T | C | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-30642A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73499134 | ||||||
| chr11:73499241
|
C | T | 1 | a0001c0001t0003g0158 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-18-30749G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73499241 | ||||||
| chr11:73499371
|
T | G | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-30879A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73499371 | ||||||
| chr11:73499464
|
TCTC | T | 29 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(26): Show | 29 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.-18-30975_-18-3097 others(7): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73499464 | ||||||
| chr11:73499485
|
G | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-30993C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73499485 | ||||||
| chr11:73499556
|
A | T | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-18-31064T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73499556 | ||||||
| chr11:73499749
|
A | C | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-31257T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73499749 | ||||||
| chr11:73499770
|
T | A | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-31278A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73499770 | ||||||
| chr11:73499893
|
C | T | 1 | a0001c0002t0001g0029 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-18-31401G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73499893 | ||||||
| chr11:73499909
|
C | T | 1 | a0001c0001t0007g0027 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-18-31417G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73499909 | ||||||
| chr11:73500137
|
C | A | 1 | a0001c0002t0005g0155 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-18-31645G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73500137 | ||||||
| chr11:73500248
|
C | T | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18-31756G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73500248 | ||||||
| chr11:73500256
|
C | CT | 17 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(14): Show | 17 | HG00140.hp2 HG01167.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.-18-31765dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73500256 | ||||||
| chr11:73500256
|
CT | C | 54 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(51): Show | 54 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.-18-31765delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73500256 | ||||||
| chr11:73500330
|
C | G | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-31838G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73500330 | ||||||
| chr11:73500480
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-18-31988C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73500480 | ||||||
| chr11:73500663
|
T | C | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-32171A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73500663 | ||||||
| chr11:73500836
|
C | T | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-32344G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73500836 | ||||||
| chr11:73501015
|
C | CA | 5 | a0001c0001t0004g0142a0001c0001t0004g0147a0001c0001t0027g0146others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-32524dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73501015 | ||||||
| chr11:73501208
|
C | T | 1 | a0001c0001t0014g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-18-32716G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73501208 | ||||||
| chr11:73501311
|
C | T | 23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-32819G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73501311 | ||||||
| chr11:73501341
|
G | C | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18-32849C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73501341 | ||||||
| chr11:73501484
|
A | T | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-18-32992T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73501484 | ||||||
| chr11:73501496
|
A | G | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-33004T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73501496 | ||||||
| chr11:73501830
|
G | A | 1 | a0001c0001t0039g0125 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-18-33338C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73501830 | ||||||
| chr11:73502188
|
C | CA | 13 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(10): Show | 13 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.-18-33697dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73502188 | ||||||
| chr11:73502680
|
G | C | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-34188C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73502680 | ||||||
| chr11:73502734
|
C | T | 1 | a0001c0002t0051g0108 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-18-34242G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73502734 | ||||||
| chr11:73502735
|
A | G | 179 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-18-34243T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73502735 | ||||||
| chr11:73502847
|
T | C | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-34355A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73502847 | ||||||
| chr11:73503471
|
G | A | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-18-34979C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73503471 | ||||||
| chr11:73503925
|
T | G | 1 | a0001c0002t0001g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-18-35433A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73503925 | ||||||
| chr11:73503932
|
G | A | 29 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(26): Show | 29 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.-18-35440C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73503932 | ||||||
| chr11:73504273
|
G | T | 179 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-18-35781C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73504273 | ||||||
| chr11:73504359
|
C | T | 2 | a0001c0001t0022g0061a0001c0001t0022g0062 | 2 | HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-18-35867G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73504359 | ||||||
| chr11:73504366
|
A | G | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-35874T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73504366 | ||||||
| chr11:73504577
|
T | C | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18-36085A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73504577 | ||||||
| chr11:73504871
|
G | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-36379C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73504871 | ||||||
| chr11:73505116
|
AT | A | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18-36625delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73505116 | ||||||
| chr11:73505215
|
T | TAAAAGTC others(3169): Show |
1 | a0001c0001t0039g0125 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-18-36724_-18-3672 others(3180): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73505215 | ||||||
| chr11:73505215
|
T | TAAAAGTC others(3156): Show |
1 | a0001c0001t0040g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18-36724_-18-3672 others(3167): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73505215 | ||||||
| chr11:73505241
|
GA | G | 34 | a0001c0001t0003g0160a0001c0001t0003g0163a0001c0001t0003g0164others(31): Show | 34 | HG00438.hp1 HG01106.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.-18-36750delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73505241 | ||||||
| chr11:73505340
|
C | A | 29 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(26): Show | 29 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.-18-36848G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73505340 | ||||||
| chr11:73505422
|
G | A | 1 | a0001c0002t0001g0053 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-18-36930C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73505422 | ||||||
| chr11:73505493
|
T | G | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18-37001A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73505493 | ||||||
| chr11:73505749
|
T | A | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18-37257A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73505749 | ||||||
| chr11:73505995
|
ATTAACCA others(6): Show |
A | 1 | a0001c0002t0001g0098 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-18-37516_-18-3750 others(17): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73505995 | ||||||
| chr11:73506106
|
A | G | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-37614T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73506106 | ||||||
| chr11:73506199
|
C | A | 4 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0001g0095others(1): Show | 4 | HG02145.hp1 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-37707G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73506199 | ||||||
| chr11:73506589
|
A | G | 2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-38097T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73506589 | ||||||
| chr11:73507185
|
G | T | 131 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(128): Show | 131 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.-18-38693C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73507185 | ||||||
| chr11:73507513
|
T | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-39021A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73507513 | ||||||
| chr11:73507614
|
T | TA | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-39123dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73507614 | ||||||
| chr11:73507649
|
A | C | 21 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(18): Show | 21 | HG02451.hp2 HG02622.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-39157T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73507649 | ||||||
| chr11:73507706
|
C | T | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-39214G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73507706 | ||||||
| chr11:73508073
|
C | T | 63 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(60): Show | 63 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.-18-39581G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73508073 | ||||||
| chr11:73508136
|
G | A | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-18-39644C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73508136 | ||||||
| chr11:73508213
|
A | T | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18-39721T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73508213 | ||||||
| chr11:73508324
|
AG | A | 10 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18-39833delC | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73508324 | ||||||
| chr11:73508372
|
T | G | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-39880A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73508372 | ||||||
| chr11:73508633
|
T | C | 60 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(57): Show | 60 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.-18-40141A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73508633 | ||||||
| chr11:73508770
|
C | T | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-18-40278G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73508770 | ||||||
| chr11:73508862
|
C | T | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-40370G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73508862 | ||||||
| chr11:73509103
|
T | C | 23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-40611A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73509103 | ||||||
| chr11:73509109
|
T | C | 1 | a0001c0001t0008g0159 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-18-40617A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73509109 | ||||||
| chr11:73509192
|
C | A | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-40700G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73509192 | ||||||
| chr11:73509203
|
T | C | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18-40711A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73509203 | ||||||
| chr11:73509750
|
C | T | 1 | a0001c0002t0001g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-18-41258G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73509750 | ||||||
| chr11:73509820
|
A | C | 3 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0007g0025 | 3 | HG01167.hp2 HG01255.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-18-41328T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73509820 | ||||||
| chr11:73509850
|
T | C | 1 | a0001c0001t0008g0175 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-18-41358A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73509850 | ||||||
| chr11:73510054
|
C | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-41562G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73510054 | ||||||
| chr11:73510089
|
A | G | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-41597T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73510089 | ||||||
| chr11:73510211
|
C | G | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-41719G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73510211 | ||||||
| chr11:73510241
|
T | G | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18-41749A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73510241 | ||||||
| chr11:73510491
|
T | C | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-41999A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73510491 | ||||||
| chr11:73510660
|
C | T | 2 | a0001c0001t0016g0135a0001c0001t0016g0136 | 2 | HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-18-42168G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73510660 | ||||||
| chr11:73510672
|
A | C | 34 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(31): Show | 34 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.-18-42180T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73510672 | ||||||
| chr11:73510676
|
G | A | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-42184C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73510676 | ||||||
| chr11:73510908
|
C | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-42416G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73510908 | ||||||
| chr11:73510912
|
A | G | 62 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 62 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(59): Show |
intron_variant | MODIFIER | c.-18-42420T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73510912 | ||||||
| chr11:73510967
|
A | G | 1 | a0001c0001t0041g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-18-42475T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73510967 | ||||||
| chr11:73511080
|
C | T | 1 | a0001c0001t0002g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-18-42588G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73511080 | ||||||
| chr11:73511088
|
T | C | 1 | a0001c0002t0001g0075 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-18-42596A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73511088 | ||||||
| chr11:73511119
|
G | A | 2 | a0001c0001t0003g0158a0001c0001t0003g0165 | 2 | NA18968.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-18-42627C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73511119 | ||||||
| chr11:73511294
|
G | C | 25 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(22): Show | 25 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18-42802C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73511294 | ||||||
| chr11:73511314
|
G | A | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-42822C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73511314 | ||||||
| chr11:73511494
|
C | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-43002G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73511494 | ||||||
| chr11:73511550
|
A | ATGTAATG others(39): Show |
1 | a0001c0001t0022g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-18-43059_-18-4305 others(50): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73511550 | ||||||
| chr11:73511550
|
A | ATGTAATG others(40): Show |
1 | a0001c0001t0022g0062 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-18-43059_-18-4305 others(51): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73511550 | ||||||
| chr11:73511550
|
A | ATGTAATG others(52): Show |
1 | a0001c0001t0024g0003 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-18-43059_-18-4305 others(63): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73511550 | ||||||
| chr11:73511550
|
A | ATGTAATG others(53): Show |
3 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004 | 3 | NA18981.hp1 NA19060.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-18-43059_-18-4305 others(64): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73511550 | ||||||
| chr11:73511679
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-18-43187G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73511679 | ||||||
| chr11:73511740
|
G | A | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18-43248C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73511740 | ||||||
| chr11:73511865
|
G | A | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-18-43373C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73511865 | ||||||
| chr11:73511898
|
G | A | 1 | a0001c0001t0041g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-18-43406C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73511898 | ||||||
| chr11:73511965
|
T | C | 2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-43473A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73511965 | ||||||
| chr11:73511999
|
C | T | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-18-43507G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73511999 | ||||||
| chr11:73512158
|
A | G | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-43666T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73512158 | ||||||
| chr11:73512555
|
G | A | 23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-44063C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73512555 | ||||||
| chr11:73512731
|
A | C | 25 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(22): Show | 25 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.-18-44239T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73512731 | ||||||
| chr11:73512748
|
G | A | 4 | a0001c0001t0004g0143a0001c0001t0004g0145a0001c0001t0026g0144others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-44256C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73512748 | ||||||
| chr11:73512892
|
C | T | 2 | a0001c0002t0001g0065a0001c0002t0001g0066 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-18-44400G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73512892 | ||||||
| chr11:73513187
|
GTTTTGTT others(16): Show |
G | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18-44718_-18-4469 others(27): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73513187 | ||||||
| chr11:73513192
|
G | T | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18-44700C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73513192 | ||||||
| chr11:73513205
|
A | AT | 15 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(12): Show | 15 | HG01884.hp1 HG01928.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18-44714dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73513205 | ||||||
| chr11:73513205
|
AT | A | 21 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(18): Show | 21 | HG00140.hp2 HG01069.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-44714delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73513205 | ||||||
| chr11:73513272
|
C | T | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-44780G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73513272 | ||||||
| chr11:73513316
|
T | C | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-44824A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73513316 | ||||||
| chr11:73513355
|
G | A | 1 | a0001c0001t0019g0070 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-18-44863C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73513355 | ||||||
| chr11:73513376
|
AT | A | 51 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(48): Show | 51 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(48): Show |
intron_variant | MODIFIER | c.-18-44885delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73513376 | ||||||
| chr11:73513454
|
GAT | G | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-44964_-18-4496 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73513454 | ||||||
| chr11:73513751
|
T | A | 1 | a0001c0002t0001g0057 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-18-45259A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73513751 | ||||||
| chr11:73514030
|
C | G | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-45538G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73514030 | ||||||
| chr11:73514092
|
G | A | 1 | a0001c0001t0034g0174 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-18-45600C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73514092 | ||||||
| chr11:73514111
|
C | T | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-18-45619G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73514111 | ||||||
| chr11:73514145
|
T | A | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-45653A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73514145 | ||||||
| chr11:73514203
|
G | T | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-45711C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73514203 | ||||||
| chr11:73514369
|
T | C | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-45877A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73514369 | ||||||
| chr11:73514418
|
T | C | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-45926A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73514418 | ||||||
| chr11:73514828
|
G | GCCAT | 23 | a0001c0001t0006g0024a0001c0001t0007g0026a0001c0001t0007g0027others(20): Show | 23 | HG00140.hp2 HG01106.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.-18-46340_-18-4633 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73514828 | ||||||
| chr11:73514828
|
GCCAT | G | 57 | a0001c0001t0002g0009a0001c0001t0003g0158a0001c0001t0003g0160others(54): Show | 57 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.-18-46340_-18-4633 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73514828 | ||||||
| chr11:73514828
|
GCCATCCA others(1): Show |
G | 18 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(15): Show | 18 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.-18-46344_-18-4633 others(12): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73514828 | ||||||
| chr11:73514828
|
GCCATCCA others(5): Show |
G | 3 | a0001c0001t0002g0011a0001c0001t0002g0016a0001c0001t0004g0145 | 3 | HG02717.hp2 HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-18-46348_-18-4633 others(16): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73514828 | ||||||
| chr11:73514982
|
A | C | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18-46490T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73514982 | ||||||
| chr11:73515025
|
T | C | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-46533A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73515025 | ||||||
| chr11:73515327
|
C | T | 1 | a0001c0001t0002g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-18-46835G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73515327 | ||||||
| chr11:73515366
|
G | A | 2 | a0001c0001t0017g0032a0001c0001t0017g0078 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-18-46874C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73515366 | ||||||
| chr11:73515370
|
G | A | 2 | a0001c0001t0003g0168a0001c0001t0003g0171 | 2 | HG00438.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-18-46878C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73515370 | ||||||
| chr11:73515399
|
C | T | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18-46907G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73515399 | ||||||
| chr11:73515456
|
C | T | 1 | a0001c0002t0048g0043 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-18-46964G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73515456 | ||||||
| chr11:73515466
|
C | A | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18-46974G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73515466 | ||||||
| chr11:73515508
|
C | CAA | 14 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(11): Show | 14 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.-18-47018_-18-4701 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73515508 | ||||||
| chr11:73515508
|
CA | C | 29 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(26): Show | 29 | HG01106.hp2 HG01515.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.-18-47017delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73515508 | ||||||
| chr11:73515627
|
A | G | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-47135T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73515627 | ||||||
| chr11:73515649
|
A | C | 1 | a0001c0002t0033g0077 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-18-47157T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73515649 | ||||||
| chr11:73515695
|
T | C | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18-47203A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73515695 | ||||||
| chr11:73515973
|
T | G | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18-47481A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73515973 | ||||||
| chr11:73515980
|
A | G | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-47488T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73515980 | ||||||
| chr11:73516034
|
G | A | 1 | a0001c0002t0012g0113 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-18-47542C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73516034 | ||||||
| chr11:73516097
|
CT | C | 10 | a0001c0001t0002g0005a0001c0001t0003g0161a0001c0001t0015g0132others(7): Show | 10 | HG00323.hp1 HG01515.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18-47606delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73516097 | ||||||
| chr11:73516099
|
T | TA | 23 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(20): Show | 23 | HG01109.hp1 HG01884.hp1 HG02572.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-47608_-18-4760 others(5): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73516099 | ||||||
| chr11:73516100
|
T | A | 169 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.-18-47608A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73516100 | ||||||
| chr11:73516242
|
A | G | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-47750T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73516242 | ||||||
| chr11:73516316
|
T | C | 60 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(57): Show | 60 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.-18-47824A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73516316 | ||||||
| chr11:73516580
|
T | C | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-48088A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73516580 | ||||||
| chr11:73516782
|
T | C | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-48290A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73516782 | ||||||
| chr11:73516870
|
C | T | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-18-48378G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73516870 | ||||||
| chr11:73517134
|
C | T | 22 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(19): Show | 22 | HG00544.hp1 HG01069.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18-48642G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73517134 | ||||||
| chr11:73517221
|
TA | T | 2 | a0001c0001t0014g0153a0001c0001t0014g0154 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-18-48730delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73517221 | ||||||
| chr11:73517242
|
G | C | 1 | a0001c0001t0041g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-18-48750C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73517242 | ||||||
| chr11:73517362
|
T | C | 9 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(6): Show | 9 | HG02055.hp2 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18-48870A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73517362 | ||||||
| chr11:73517375
|
C | T | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18-48883G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73517375 | ||||||
| chr11:73517511
|
T | C | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-49019A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73517511 | ||||||
| chr11:73517537
|
C | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-49045G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73517537 | ||||||
| chr11:73517560
|
A | G | 6 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-49068T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73517560 | ||||||
| chr11:73517633
|
T | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18-49141A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73517633 | ||||||
| chr11:73517640
|
T | C | 93 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(90): Show | 93 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.-18-49148A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73517640 | ||||||
| chr11:73517712
|
C | T | 3 | a0001c0001t0016g0135a0001c0001t0016g0136a0001c0001t0041g0134 | 3 | HG02615.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-18-49220G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73517712 | ||||||
| chr11:73517754
|
G | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-49262C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73517754 | ||||||
| chr11:73517756
|
C | A | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-49264G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73517756 | ||||||
| chr11:73517859
|
G | A | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-49367C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73517859 | ||||||
| chr11:73518025
|
C | T | 1 | a0001c0002t0005g0155 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-18-49533G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73518025 | ||||||
| chr11:73518032
|
T | C | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-49540A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73518032 | ||||||
| chr11:73518193
|
C | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-49701G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73518193 | ||||||
| chr11:73518323
|
C | A | 1 | a0001c0002t0001g0034 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-18-49831G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73518323 | ||||||
| chr11:73518324
|
C | T | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-49832G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73518324 | ||||||
| chr11:73518387
|
CATTAAAA | C | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-49902_-18-4989 others(11): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73518387 | ||||||
| chr11:73518581
|
T | A | 4 | a0001c0002t0001g0071a0001c0002t0001g0121a0001c0002t0001g0122others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-50089A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73518581 | ||||||
| chr11:73518989
|
C | A | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18-50497G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73518989 | ||||||
| chr11:73518994
|
C | G | 1 | a0001c0002t0001g0031 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-18-50502G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73518994 | ||||||
| chr11:73519018
|
C | T | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-18-50526G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73519018 | ||||||
| chr11:73519025
|
C | G | 1 | a0001c0002t0009g0076 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-18-50533G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73519025 | ||||||
| chr11:73519134
|
T | C | 23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-50642A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73519134 | ||||||
| chr11:73519331
|
A | G | 1 | a0001c0006t0001g0083 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-18-50839T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73519331 | ||||||
| chr11:73519366
|
C | G | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-50874G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73519366 | ||||||
| chr11:73519547
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-18-51055C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73519547 | ||||||
| chr11:73519581
|
A | T | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-51089T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73519581 | ||||||
| chr11:73519694
|
A | C | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18-51202T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73519694 | ||||||
| chr11:73519695
|
G | A | 23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-51203C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73519695 | ||||||
| chr11:73519778
|
ATG | A | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-18-51288_-18-5128 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73519778 | ||||||
| chr11:73519782
|
G | A | 1 | a0001c0002t0009g0076 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-18-51290C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73519782 | ||||||
| chr11:73519787
|
T | C | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-51295A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73519787 | ||||||
| chr11:73519796
|
G | A | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18-51304C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73519796 | ||||||
| chr11:73519954
|
C | A | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-51462G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73519954 | ||||||
| chr11:73520611
|
C | T | 1 | a0001c0002t0013g0103 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-18-52119G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73520611 | ||||||
| chr11:73520840
|
G | T | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-52348C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73520840 | ||||||
| chr11:73520908
|
T | TA | 8 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(5): Show | 8 | HG01106.hp2 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18-52417dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73520908 | ||||||
| chr11:73521170
|
G | A | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18-52678C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73521170 | ||||||
| chr11:73521368
|
T | C | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18-52876A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73521368 | ||||||
| chr11:73521476
|
AAAG | A | 3 | a0001c0002t0001g0118a0001c0002t0012g0082a0001c0002t0012g0113 | 3 | NA19056.hp1 NA19083.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-18-52987_-18-5298 others(7): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73521476 | ||||||
| chr11:73521512
|
T | A | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-53020A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73521512 | ||||||
| chr11:73521518
|
G | C | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-53026C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73521518 | ||||||
| chr11:73521624
|
T | G | 2 | a0001c0001t0007g0022a0001c0001t0007g0023 | 2 | HG01167.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-18-53132A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73521624 | ||||||
| chr11:73521652
|
G | A | 2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-18-53160C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73521652 | ||||||
| chr11:73521692
|
G | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-53200C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73521692 | ||||||
| chr11:73521868
|
T | C | 1 | a0001c0002t0001g0091 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-18-53376A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73521868 | ||||||
| chr11:73521937
|
G | C | 1 | a0001c0002t0001g0053 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-18-53445C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73521937 | ||||||
| chr11:73522133
|
C | T | 1 | a0001c0001t0004g0142 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-18-53641G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73522133 | ||||||
| chr11:73522175
|
T | C | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-53683A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73522175 | ||||||
| chr11:73522203
|
C | CA | 151 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(148): Show | 151 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-18-53712dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73522203 | ||||||
| chr11:73522203
|
C | CAA | 24 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(21): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-18-53713_-18-5371 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73522203 | ||||||
| chr11:73522218
|
T | A | 2 | a0001c0001t0002g0011a0001c0001t0002g0016 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-18-53726A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73522218 | ||||||
| chr11:73522237
|
G | A | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18-53745C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73522237 | ||||||
| chr11:73522286
|
A | G | 1 | a0001c0001t0014g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-18-53794T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73522286 | ||||||
| chr11:73522317
|
T | G | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-53825A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73522317 | ||||||
| chr11:73522389
|
G | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-53897C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73522389 | ||||||
| chr11:73522489
|
A | G | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-53997T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73522489 | ||||||
| chr11:73522679
|
T | C | 26 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(23): Show | 26 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18-54187A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73522679 | ||||||
| chr11:73522810
|
T | C | 156 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.-18-54318A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73522810 | ||||||
| chr11:73522994
|
C | T | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-54502G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73522994 | ||||||
| chr11:73523128
|
G | A | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-54636C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73523128 | ||||||
| chr11:73523138
|
G | A | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18-54646C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73523138 | ||||||
| chr11:73523268
|
G | T | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-18-54776C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73523268 | ||||||
| chr11:73523351
|
C | T | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18-54859G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73523351 | ||||||
| chr11:73523492
|
T | C | 1 | a0001c0002t0001g0065 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-18-55000A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73523492 | ||||||
| chr11:73523635
|
G | A | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18-55143C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73523635 | ||||||
| chr11:73523864
|
A | AT | 99 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(96): Show | 99 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.-18-55373dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73523864 | ||||||
| chr11:73523864
|
A | ATT | 47 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(44): Show | 47 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-18-55374_-18-5537 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73523864 | ||||||
| chr11:73523864
|
A | ATTT | 26 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(23): Show | 26 | HG01884.hp1 HG02109.hp2 HG02572.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18-55375_-18-5537 others(7): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73523864 | ||||||
| chr11:73523864
|
A | ATTTT | 6 | a0001c0001t0015g0132a0001c0001t0015g0133a0001c0001t0019g0069others(3): Show | 6 | HG01106.hp2 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-55376_-18-5537 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73523864 | ||||||
| chr11:73524028
|
AC | A | 5 | a0001c0001t0003g0160a0001c0001t0003g0163a0001c0001t0003g0164others(2): Show | 5 | NA18977.hp1 NA18983.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18-55537delG | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73524028 | ||||||
| chr11:73524504
|
CT | C | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-56013delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73524504 | ||||||
| chr11:73524517
|
C | A | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-18-56025G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73524517 | ||||||
| chr11:73524554
|
T | G | 5 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0025g0120others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-56062A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73524554 | ||||||
| chr11:73524632
|
C | T | 10 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18-56140G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73524632 | ||||||
| chr11:73524747
|
G | A | 1 | a0001c0002t0001g0087 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-18-56255C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73524747 | ||||||
| chr11:73524790
|
G | C | 2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-18-56298C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73524790 | ||||||
| chr11:73525021
|
AT | A | 81 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(78): Show | 81 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.-18-56530delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73525021 | ||||||
| chr11:73525079
|
C | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-56587G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73525079 | ||||||
| chr11:73525182
|
A | T | 1 | a0001c0001t0006g0180 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-18-56690T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73525182 | ||||||
| chr11:73525223
|
A | G | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-56731T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73525223 | ||||||
| chr11:73525231
|
A | G | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-56739T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73525231 | ||||||
| chr11:73525722
|
C | T | 3 | a0001c0002t0005g0047a0001c0002t0005g0048a0001c0002t0038g0041 | 3 | HG01928.hp1 HG01934.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-18-57230G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73525722 | ||||||
| chr11:73525772
|
G | C | 26 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(23): Show | 26 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18-57280C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73525772 | ||||||
| chr11:73526454
|
G | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-57962C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73526454 | ||||||
| chr11:73526456
|
T | C | 1 | a0001c0001t0003g0176 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-18-57964A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73526456 | ||||||
| chr11:73526860
|
C | T | 2 | a0001c0001t0014g0153a0001c0001t0014g0154 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-18-58368G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73526860 | ||||||
| chr11:73526868
|
C | CA | 28 | a0001c0001t0030g0156a0001c0002t0001g0034a0001c0002t0001g0035others(25): Show | 28 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.-18-58377dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73526868 | ||||||
| chr11:73526868
|
C | CAA | 10 | a0001c0002t0001g0033a0001c0002t0001g0036a0001c0002t0001g0038others(7): Show | 10 | HG01106.hp1 HG01255.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18-58378_-18-5837 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73526868 | ||||||
| chr11:73526868
|
CA | C | 24 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(21): Show | 24 | HG00140.hp2 HG01934.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.-18-58377delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73526868 | ||||||
| chr11:73526868
|
CAA | C | 52 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(49): Show | 52 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.-18-58378_-18-5837 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73526868 | ||||||
| chr11:73526868
|
CAAA | C | 10 | a0001c0001t0003g0158a0001c0001t0004g0142a0001c0001t0004g0143others(7): Show | 10 | HG01515.hp2 HG01517.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18-58379_-18-5837 others(7): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73526868 | ||||||
| chr11:73526898
|
G | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-58406C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73526898 | ||||||
| chr11:73526987
|
G | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-58495C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73526987 | ||||||
| chr11:73527119
|
TTG | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-58629_-18-5862 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73527119 | ||||||
| chr11:73527325
|
A | G | 2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-58833T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73527325 | ||||||
| chr11:73527361
|
C | T | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18-58869G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73527361 | ||||||
| chr11:73527543
|
A | C | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-59051T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73527543 | ||||||
| chr11:73527600
|
G | A | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-59108C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73527600 | ||||||
| chr11:73527622
|
C | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-59130G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73527622 | ||||||
| chr11:73527960
|
T | C | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-59468A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73527960 | ||||||
| chr11:73528057
|
T | G | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-18-59565A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73528057 | ||||||
| chr11:73528162
|
A | G | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-59670T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73528162 | ||||||
| chr11:73528210
|
G | C | 1 | a0001c0001t0008g0159 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-18-59718C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73528210 | ||||||
| chr11:73528213
|
C | T | 1 | a0001c0001t0007g0025 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-18-59721G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73528213 | ||||||
| chr11:73528227
|
A | G | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-59735T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73528227 | ||||||
| chr11:73528249
|
T | G | 1 | a0001c0001t0004g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-18-59757A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73528249 | ||||||
| chr11:73528648
|
C | A | 3 | a0001c0001t0004g0142a0001c0001t0004g0147a0001c0001t0027g0146 | 3 | HG02717.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-18-60156G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73528648 | ||||||
| chr11:73528862
|
TG | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-60371delC | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73528862 | ||||||
| chr11:73528906
|
A | C | 1 | a0001c0001t0022g0062 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-18-60414T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73528906 | ||||||
| chr11:73529026
|
G | C | 3 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0028 | 3 | HG02451.hp1 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-18-60534C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73529026 | ||||||
| chr11:73529030
|
C | T | 2 | a0001c0001t0022g0061a0001c0001t0022g0062 | 2 | HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-18-60538G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73529030 | ||||||
| chr11:73529074
|
G | T | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18-60582C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73529074 | ||||||
| chr11:73529133
|
T | C | 2 | a0001c0001t0006g0024a0001c0001t0006g0180 | 2 | HG00140.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-18-60641A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73529133 | ||||||
| chr11:73529227
|
T | C | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18-60735A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73529227 | ||||||
| chr11:73529234
|
C | T | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18-60742G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73529234 | ||||||
| chr11:73529463
|
G | A | 1 | a0001c0002t0001g0046 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-18-60971C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73529463 | ||||||
| chr11:73529719
|
G | C | 23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-18-61227C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73529719 | ||||||
| chr11:73529796
|
C | CTTT | 19 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(16): Show | 19 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18-61307_-18-6130 others(7): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73529796 | ||||||
| chr11:73529796
|
C | CTTTTTTT others(2): Show |
13 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(10): Show | 13 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18-61313_-18-6130 others(13): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73529796 | ||||||
| chr11:73529796
|
C | CTTTTTTT others(3): Show |
21 | a0001c0001t0002g0016a0001c0001t0006g0020a0001c0001t0006g0021others(18): Show | 21 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-61314_-18-6130 others(14): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73529796 | ||||||
| chr11:73529796
|
C | CTTTTTTT others(4): Show |
18 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(15): Show | 18 | HG02109.hp2 HG02451.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.-18-61315_-18-6130 others(15): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73529796 | ||||||
| chr11:73529796
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0030g0156others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-61316_-18-6130 others(16): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73529796 | ||||||
| chr11:73529796
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0039g0125a0001c0001t0040g0126a0001c0001t0042g0060 | 3 | HG02055.hp2 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-18-61317_-18-6130 others(17): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73529796 | ||||||
| chr11:73529796
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0041g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-18-61305_-18-6130 others(31): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73529796 | ||||||
| chr11:73530054
|
C | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-61562G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73530054 | ||||||
| chr11:73530136
|
C | T | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-61644G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73530136 | ||||||
| chr11:73530158
|
C | T | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-61666G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73530158 | ||||||
| chr11:73530261
|
C | T | 2 | a0001c0001t0022g0061a0001c0001t0022g0062 | 2 | HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-18-61769G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73530261 | ||||||
| chr11:73530262
|
C | A | 1 | a0001c0001t0002g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-18-61770G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73530262 | ||||||
| chr11:73530330
|
GGAGC | G | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-61842_-18-6183 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73530330 | ||||||
| chr11:73530433
|
G | C | 1 | a0001c0002t0001g0117 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-18-61941C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73530433 | ||||||
| chr11:73530681
|
T | C | 1 | a0001c0002t0001g0065 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-18-62189A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73530681 | ||||||
| chr11:73530995
|
C | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18-62503G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73530995 | ||||||
| chr11:73531129
|
G | A | 1 | a0001c0002t0001g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-18-62637C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73531129 | ||||||
| chr11:73531177
|
T | A | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18-62685A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73531177 | ||||||
| chr11:73531410
|
T | C | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-62918A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73531410 | ||||||
| chr11:73531802
|
C | CT | 46 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(43): Show | 46 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.-18-63311dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73531802 | ||||||
| chr11:73531802
|
C | CTT | 8 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18-63312_-18-6331 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73531802 | ||||||
| chr11:73531802
|
C | CTTTT | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-63314_-18-6331 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73531802 | ||||||
| chr11:73531802
|
CT | C | 26 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(23): Show | 26 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.-18-63311delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73531802 | ||||||
| chr11:73531830
|
G | C | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18-63338C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73531830 | ||||||
| chr11:73531971
|
A | AT | 28 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(25): Show | 28 | HG00438.hp1 HG00544.hp2 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18-63480dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73531971 | ||||||
| chr11:73531971
|
AT | A | 5 | a0001c0001t0002g0010a0001c0001t0014g0154a0001c0002t0001g0034others(2): Show | 5 | HG01257.hp1 HG01515.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18-63480delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73531971 | ||||||
| chr11:73532016
|
T | C | 1 | a0001c0002t0005g0110 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-18-63524A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73532016 | ||||||
| chr11:73532108
|
T | C | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18-63616A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73532108 | ||||||
| chr11:73532429
|
A | G | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-18-63937T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73532429 | ||||||
| chr11:73532520
|
T | C | 22 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(19): Show | 22 | HG00544.hp1 HG01069.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.-18-64028A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73532520 | ||||||
| chr11:73532570
|
A | G | 8 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18-64078T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73532570 | ||||||
| chr11:73533185
|
C | T | 66 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(63): Show | 66 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(63): Show |
intron_variant | MODIFIER | c.-18-64693G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73533185 | ||||||
| chr11:73533298
|
G | A | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+64625C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73533298 | ||||||
| chr11:73533467
|
C | A | 179 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-19+64456G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73533467 | ||||||
| chr11:73533507
|
C | A | 179 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-19+64416G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73533507 | ||||||
| chr11:73533525
|
C | A | 179 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-19+64398G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73533525 | ||||||
| chr11:73533547
|
C | A | 179 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-19+64376G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73533547 | ||||||
| chr11:73533565
|
GC | G | 30 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(27): Show | 30 | HG00323.hp1 HG00544.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19+64357delG | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73533565 | ||||||
| chr11:73533566
|
CCA | C | 62 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 62 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(59): Show |
intron_variant | MODIFIER | c.-19+64355_-19+6435 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73533566 | ||||||
| chr11:73533567
|
C | A | 87 | a0001c0001t0003g0168a0001c0002t0001g0029a0001c0002t0001g0031others(84): Show | 87 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-19+64356G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73533567 | ||||||
| chr11:73533998
|
T | A | 1 | a0001c0002t0001g0122 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-19+63925A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73533998 | ||||||
| chr11:73534097
|
T | C | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-19+63826A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73534097 | ||||||
| chr11:73534113
|
G | A | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-19+63810C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73534113 | ||||||
| chr11:73534144
|
T | C | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-19+63779A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73534144 | ||||||
| chr11:73534407
|
A | AT | 19 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(16): Show | 19 | HG00140.hp1 HG01106.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-19+63515dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73534407 | ||||||
| chr11:73534407
|
A | T | 3 | a0001c0001t0003g0171a0001c0001t0007g0026a0001c0001t0007g0027 | 3 | HG02683.hp1 HG03239.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-19+63516T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73534407 | ||||||
| chr11:73534411
|
T | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+63512A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73534411 | ||||||
| chr11:73534447
|
G | A | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+63476C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73534447 | ||||||
| chr11:73534455
|
C | T | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-19+63468G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73534455 | ||||||
| chr11:73534482
|
A | T | 2 | a0001c0002t0001g0106a0001c0002t0032g0116 | 2 | HG02109.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-19+63441T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73534482 | ||||||
| chr11:73534527
|
C | T | 1 | a0001c0002t0001g0119 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-19+63396G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73534527 | ||||||
| chr11:73534600
|
G | A | 3 | a0001c0001t0016g0135a0001c0001t0016g0136a0001c0001t0041g0134 | 3 | HG02615.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-19+63323C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73534600 | ||||||
| chr11:73534679
|
AG | A | 179 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-19+63243delC | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73534679 | ||||||
| chr11:73534700
|
G | A | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19+63223C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73534700 | ||||||
| chr11:73534724
|
G | A | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+63199C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73534724 | ||||||
| chr11:73535032
|
G | A | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-19+62891C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73535032 | ||||||
| chr11:73535418
|
CT | C | 16 | a0001c0001t0003g0169a0001c0001t0011g0149a0001c0001t0011g0150others(13): Show | 16 | HG02055.hp1 HG02258.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+62504delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73535418 | ||||||
| chr11:73535418
|
CTT | C | 55 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(52): Show | 55 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.-19+62503_-19+6250 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73535418 | ||||||
| chr11:73535513
|
G | A | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+62410C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73535513 | ||||||
| chr11:73535580
|
C | T | 3 | a0001c0002t0013g0101a0001c0002t0013g0102a0001c0002t0013g0103 | 3 | HG02258.hp1 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-19+62343G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73535580 | ||||||
| chr11:73535609
|
C | T | 27 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(24): Show | 27 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.-19+62314G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73535609 | ||||||
| chr11:73535648
|
T | C | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+62275A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73535648 | ||||||
| chr11:73535663
|
C | T | 1 | a0002c0005t0001g0055 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-19+62260G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73535663 | ||||||
| chr11:73535722
|
C | CT | 46 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0162others(43): Show | 46 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-19+62200dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73535722 | ||||||
| chr11:73535722
|
CT | C | 96 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(93): Show | 96 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.-19+62200delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73535722 | ||||||
| chr11:73535873
|
AT | A | 61 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(58): Show | 61 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.-19+62049delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73535873 | ||||||
| chr11:73535974
|
T | A | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+61949A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73535974 | ||||||
| chr11:73536138
|
A | C | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+61785T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73536138 | ||||||
| chr11:73536415
|
C | T | 1 | a0001c0002t0009g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-19+61508G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73536415 | ||||||
| chr11:73536588
|
G | A | 1 | a0001c0002t0001g0031 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-19+61335C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73536588 | ||||||
| chr11:73536755
|
T | G | 1 | a0001c0002t0001g0099 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-19+61168A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73536755 | ||||||
| chr11:73537041
|
A | G | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19+60882T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73537041 | ||||||
| chr11:73537224
|
A | C | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19+60699T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73537224 | ||||||
| chr11:73537404
|
T | C | 1 | a0001c0002t0005g0110 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-19+60519A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73537404 | ||||||
| chr11:73537418
|
G | A | 3 | a0001c0001t0011g0148a0001c0001t0011g0149a0001c0001t0011g0150 | 3 | HG02895.hp2 HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-19+60505C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73537418 | ||||||
| chr11:73537516
|
T | C | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+60407A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73537516 | ||||||
| chr11:73537525
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-19+60398G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73537525 | ||||||
| chr11:73537597
|
T | C | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-19+60326A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73537597 | ||||||
| chr11:73537628
|
A | C | 60 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(57): Show | 60 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.-19+60295T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73537628 | ||||||
| chr11:73537647
|
T | C | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-19+60276A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73537647 | ||||||
| chr11:73537658
|
C | T | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-19+60265G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73537658 | ||||||
| chr11:73537940
|
A | G | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+59983T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73537940 | ||||||
| chr11:73537972
|
C | T | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19+59951G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73537972 | ||||||
| chr11:73538027
|
A | C | 3 | a0001c0001t0003g0163a0001c0001t0003g0164a0001c0001t0003g0166 | 3 | NA18977.hp1 NA18983.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-19+59896T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73538027 | ||||||
| chr11:73538068
|
T | C | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+59855A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73538068 | ||||||
| chr11:73538333
|
AC | A | 33 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(30): Show | 33 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.-19+59589delG | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73538333 | ||||||
| chr11:73538334
|
C | A | 59 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(56): Show | 59 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.-19+59589G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73538334 | ||||||
| chr11:73538340
|
A | C | 5 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0022g0061others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+59583T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73538340 | ||||||
| chr11:73538341
|
C | A | 1 | a0001c0001t0022g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-19+59582G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73538341 | ||||||
| chr11:73538347
|
A | C | 6 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+59576T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73538347 | ||||||
| chr11:73538352
|
A | G | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-19+59571T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73538352 | ||||||
| chr11:73538358
|
G | A | 2 | a0001c0002t0001g0118a0001c0002t0012g0082 | 2 | NA19056.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-19+59565C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73538358 | ||||||
| chr11:73538455
|
T | C | 1 | a0001c0002t0013g0103 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-19+59468A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73538455 | ||||||
| chr11:73538783
|
C | T | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-19+59140G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73538783 | ||||||
| chr11:73538807
|
G | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+59116C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73538807 | ||||||
| chr11:73538865
|
A | G | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-19+59058T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73538865 | ||||||
| chr11:73539267
|
ATTTT | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+58652_-19+5865 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73539267 | ||||||
| chr11:73539621
|
T | G | 1 | a0001c0001t0022g0062 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-19+58302A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73539621 | ||||||
| chr11:73539683
|
C | T | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+58240G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73539683 | ||||||
| chr11:73539709
|
T | A | 4 | a0001c0002t0001g0071a0001c0002t0001g0121a0001c0002t0001g0122others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+58214A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73539709 | ||||||
| chr11:73539852
|
T | C | 1 | a0001c0002t0033g0077 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-19+58071A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73539852 | ||||||
| chr11:73540014
|
G | A | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-19+57909C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73540014 | ||||||
| chr11:73540261
|
C | T | 179 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-19+57662G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73540261 | ||||||
| chr11:73540325
|
G | A | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+57598C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73540325 | ||||||
| chr11:73540496
|
A | G | 1 | a0001c0002t0001g0087 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-19+57427T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73540496 | ||||||
| chr11:73540657
|
T | C | 1 | a0001c0002t0001g0029 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-19+57266A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73540657 | ||||||
| chr11:73540801
|
T | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+57122A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73540801 | ||||||
| chr11:73540864
|
G | T | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+57059C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73540864 | ||||||
| chr11:73541022
|
T | C | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+56901A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73541022 | ||||||
| chr11:73541131
|
C | T | 2 | a0001c0002t0001g0088a0001c0002t0001g0091 | 2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-19+56792G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73541131 | ||||||
| chr11:73541132
|
G | A | 1 | a0001c0001t0007g0025 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-19+56791C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73541132 | ||||||
| chr11:73541190
|
G | C | 1 | a0001c0002t0051g0108 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-19+56733C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73541190 | ||||||
| chr11:73541273
|
C | T | 1 | a0001c0002t0009g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-19+56650G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73541273 | ||||||
| chr11:73541281
|
TAGAA | T | 24 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(21): Show | 24 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+56638_-19+5664 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73541281 | ||||||
| chr11:73541364
|
C | T | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+56559G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73541364 | ||||||
| chr11:73541518
|
G | A | 2 | a0001c0001t0008g0172a0001c0001t0008g0173 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-19+56405C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73541518 | ||||||
| chr11:73541593
|
G | T | 1 | a0001c0002t0012g0113 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-19+56330C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73541593 | ||||||
| chr11:73541731
|
T | TGTTATGA others(36): Show |
1 | a0001c0002t0001g0053 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-19+56149_-19+5619 others(47): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73541731 | ||||||
| chr11:73541738
|
A | G | 3 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0028 | 3 | HG02451.hp1 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-19+56185T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73541738 | ||||||
| chr11:73541902
|
C | G | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+56021G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73541902 | ||||||
| chr11:73542252
|
T | A | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-19+55671A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73542252 | ||||||
| chr11:73542253
|
T | A | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-19+55670A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73542253 | ||||||
| chr11:73542271
|
T | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-19+55652A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73542271 | ||||||
| chr11:73542284
|
A | G | 1 | a0001c0001t0022g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-19+55639T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73542284 | ||||||
| chr11:73542507
|
C | T | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+55416G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73542507 | ||||||
| chr11:73542910
|
T | C | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+55013A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73542910 | ||||||
| chr11:73542997
|
A | G | 11 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(8): Show | 11 | HG01884.hp1 HG02717.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+54926T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73542997 | ||||||
| chr11:73543067
|
T | C | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+54856A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73543067 | ||||||
| chr11:73543169
|
C | T | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19+54754G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73543169 | ||||||
| chr11:73543182
|
A | G | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+54741T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73543182 | ||||||
| chr11:73543262
|
C | CT | 57 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(54): Show | 57 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.-19+54660dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73543262 | ||||||
| chr11:73543262
|
C | CTT | 29 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(26): Show | 29 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-19+54659_-19+5466 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73543262 | ||||||
| chr11:73543396
|
G | T | 2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-19+54527C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73543396 | ||||||
| chr11:73543553
|
G | A | 58 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(55): Show | 58 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.-19+54370C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73543553 | ||||||
| chr11:73543871
|
A | G | 5 | a0001c0001t0003g0160a0001c0001t0003g0163a0001c0001t0003g0164others(2): Show | 5 | NA18977.hp1 NA18983.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+54052T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73543871 | ||||||
| chr11:73543881
|
C | A | 1 | a0001c0001t0043g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-19+54042G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73543881 | ||||||
| chr11:73544031
|
C | G | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+53892G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544031 | ||||||
| chr11:73544454
|
C | CTA | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+53467_-19+5346 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544454 | ||||||
| chr11:73544658
|
C | T | 1 | a0001c0003t0004g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-19+53265G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544658 | ||||||
| chr11:73544663
|
A | ATTATATA others(22): Show |
1 | a0001c0002t0051g0108 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-19+53231_-19+5325 others(33): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544663 | ||||||
| chr11:73544663
|
A | T | 1 | a0001c0003t0004g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-19+53260T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544663 | ||||||
| chr11:73544670
|
A | ATAATTAT others(22): Show |
1 | a0001c0002t0021g0054 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-19+53224_-19+5325 others(33): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544670 | ||||||
| chr11:73544670
|
A | G | 1 | a0001c0003t0004g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-19+53253T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544670 | ||||||
| chr11:73544670
|
ATAATTAT others(22): Show |
A | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+53224_-19+5325 others(33): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544670 | ||||||
| chr11:73544694
|
T | G | 1 | a0001c0001t0011g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-19+53229A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544694 | ||||||
| chr11:73544699
|
G | A | 5 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0025g0120others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+53224C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544699 | ||||||
| chr11:73544728
|
G | A | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-19+53195C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544728 | ||||||
| chr11:73544728
|
G | GTAATTAT others(32): Show |
2 | a0001c0002t0001g0071a0001c0002t0001g0079 | 2 | HG02145.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.-19+53156_-19+5319 others(43): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544728 | ||||||
| chr11:73544728
|
G | GTAATTAT others(61): Show |
2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+53194_-19+5319 others(72): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544728 | ||||||
| chr11:73544736
|
A | G | 1 | a0001c0001t0037g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-19+53187T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544736 | ||||||
| chr11:73544772
|
T | TATATATA others(70): Show |
15 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(12): Show | 15 | HG01884.hp1 HG02572.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+53150_-19+5315 others(81): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544772 | ||||||
| chr11:73544772
|
T | TATATATA others(108): Show |
1 | a0001c0001t0004g0142 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-19+53150_-19+5315 others(119): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544772 | ||||||
| chr11:73544772
|
T | TATATATA others(31): Show |
3 | a0001c0001t0030g0156a0001c0003t0004g0063a0001c0003t0028g0064 | 3 | HG02109.hp2 HG02615.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-19+53113_-19+5315 others(42): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544772 | ||||||
| chr11:73544772
|
T | TATATATT others(60): Show |
3 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060 | 3 | HG01106.hp2 HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-19+53150_-19+5315 others(71): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544772 | ||||||
| chr11:73544772
|
T | TATATATT others(50): Show |
2 | a0001c0001t0014g0153a0001c0001t0014g0154 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-19+53150_-19+5315 others(61): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544772 | ||||||
| chr11:73544772
|
T | TATATATT others(89): Show |
2 | a0001c0001t0025g0120a0001c0001t0043g0068 | 2 | HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-19+53150_-19+5315 others(100): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544772 | ||||||
| chr11:73544772
|
T | TATATATT others(79): Show |
2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+53150_-19+5315 others(90): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544772 | ||||||
| chr11:73544832
|
T | C | 1 | a0001c0002t0001g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-19+53091A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544832 | ||||||
| chr11:73544845
|
AAATATAT | A | 17 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(14): Show | 17 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.-19+53071_-19+5307 others(11): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544845 | ||||||
| chr11:73544861
|
A | AT | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+53061dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544861 | ||||||
| chr11:73544861
|
A | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+53062T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544861 | ||||||
| chr11:73544866
|
TA | T | 3 | a0001c0001t0006g0067a0001c0001t0039g0125a0001c0001t0040g0126 | 3 | HG02055.hp2 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-19+53056delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544866 | ||||||
| chr11:73544867
|
A | ATATTATA others(22): Show |
15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+53055_-19+5305 others(33): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544867 | ||||||
| chr11:73544870
|
T | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+53053A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544870 | ||||||
| chr11:73544880
|
A | T | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+53043T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544880 | ||||||
| chr11:73544880
|
ATATATAA others(28): Show |
A | 1 | a0001c0002t0009g0076 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-19+53008_-19+5304 others(39): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544880 | ||||||
| chr11:73544891
|
A | G | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+53032T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544891 | ||||||
| chr11:73544895
|
A | T | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-19+53028T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544895 | ||||||
| chr11:73544895
|
AATATATT others(7): Show |
A | 2 | a0001c0002t0001g0053a0001c0002t0021g0104 | 2 | HG02083.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.-19+53014_-19+5302 others(18): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544895 | ||||||
| chr11:73544896
|
ATATAT | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+53022_-19+5302 others(9): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544896 | ||||||
| chr11:73544917
|
A | T | 2 | a0001c0001t0014g0153a0001c0001t0014g0154 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-19+53006T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544917 | ||||||
| chr11:73544937
|
TATGTA | T | 3 | a0001c0001t0016g0135a0001c0001t0016g0136a0001c0001t0041g0134 | 3 | HG02615.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-19+52981_-19+5298 others(9): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544937 | ||||||
| chr11:73544940
|
G | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+52983C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544940 | ||||||
| chr11:73544947
|
A | ATATTATA others(95): Show |
2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+52975_-19+5297 others(106): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544947 | ||||||
| chr11:73544949
|
A | T | 1 | a0001c0002t0001g0065 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-19+52974T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544949 | ||||||
| chr11:73544956
|
T | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+52967A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544956 | ||||||
| chr11:73544957
|
A | T | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+52966T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544957 | ||||||
| chr11:73544970
|
A | T | 1 | a0001c0001t0003g0176 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-19+52953T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544970 | ||||||
| chr11:73544971
|
T | A | 1 | a0001c0001t0003g0176 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-19+52952A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544971 | ||||||
| chr11:73544977
|
A | ATTTTATA others(80): Show |
4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+52945_-19+5294 others(91): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544977 | ||||||
| chr11:73544979
|
T | A | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+52944A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544979 | ||||||
| chr11:73544984
|
T | A | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+52939A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544984 | ||||||
| chr11:73544985
|
T | A | 2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-19+52938A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544985 | ||||||
| chr11:73544994
|
G | A | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+52929C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544994 | ||||||
| chr11:73544994
|
G | GTATATAT others(113): Show |
1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-19+52928_-19+5292 others(124): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544994 | ||||||
| chr11:73544994
|
G | GTATATAT others(87): Show |
4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+52928_-19+5292 others(98): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544994 | ||||||
| chr11:73544994
|
G | GTATATAT others(85): Show |
8 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+52928_-19+5292 others(96): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544994 | ||||||
| chr11:73544994
|
G | GTATATAT others(101): Show |
5 | a0001c0001t0004g0142a0001c0001t0004g0147a0001c0001t0004g0151others(2): Show | 5 | HG02717.hp1 HG02896.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+52928_-19+5292 others(112): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544994 | ||||||
| chr11:73544994
|
G | GTATATAT others(122): Show |
2 | a0001c0001t0011g0149a0001c0001t0011g0150 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-19+52928_-19+5292 others(133): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544994 | ||||||
| chr11:73544994
|
G | GTATATAT others(124): Show |
1 | a0001c0001t0011g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-19+52928_-19+5292 others(135): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73544994 | ||||||
| chr11:73545002
|
A | AATATATA others(65): Show |
1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-19+52920_-19+5292 others(76): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545002 | ||||||
| chr11:73545002
|
A | AATT | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19+52920_-19+5292 others(7): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545002 | ||||||
| chr11:73545002
|
A | AATTATAT others(120): Show |
3 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0007g0025 | 3 | HG01167.hp2 HG01255.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-19+52920_-19+5292 others(131): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545002 | ||||||
| chr11:73545002
|
A | AATTATAT others(121): Show |
2 | a0001c0001t0007g0026a0001c0001t0007g0027 | 2 | HG02683.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-19+52920_-19+5292 others(132): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545002 | ||||||
| chr11:73545002
|
A | AATTATAT others(123): Show |
5 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(2): Show | 5 | HG00140.hp2 HG02451.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+52920_-19+5292 others(134): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545002 | ||||||
| chr11:73545002
|
A | AATTATAT others(173): Show |
1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-19+52920_-19+5292 others(184): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545002 | ||||||
| chr11:73545002
|
A | AATTATAT others(195): Show |
3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0017 | 3 | HG02451.hp2 HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-19+52920_-19+5292 others(206): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545002 | ||||||
| chr11:73545002
|
A | AATTATAT others(197): Show |
1 | a0001c0001t0002g0016 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-19+52920_-19+5292 others(208): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545002 | ||||||
| chr11:73545004
|
T | TTATATAT others(198): Show |
1 | a0001c0001t0002g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-19+52918_-19+5291 others(209): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545004 | ||||||
| chr11:73545004
|
T | TTATATAT others(198): Show |
1 | a0001c0001t0002g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-19+52918_-19+5291 others(209): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545004 | ||||||
| chr11:73545004
|
T | TTATATAT others(200): Show |
6 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(3): Show | 6 | HG02723.hp2 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+52918_-19+5291 others(211): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545004 | ||||||
| chr11:73545004
|
T | TTATATAT others(198): Show |
1 | a0001c0001t0002g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19+52918_-19+5291 others(209): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545004 | ||||||
| chr11:73545004
|
T | TTATATAT others(198): Show |
2 | a0001c0001t0002g0005a0001c0001t0002g0015 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-19+52918_-19+5291 others(209): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545004 | ||||||
| chr11:73545007
|
AC | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(8): Show | 11 | HG02723.hp2 HG02809.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+52915delG | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545007 | ||||||
| chr11:73545008
|
C | A | 17 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0016others(14): Show | 17 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19+52915G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545008 | ||||||
| chr11:73545008
|
C | CTATATAT others(36): Show |
1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-19+52914_-19+5291 others(47): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545008 | ||||||
| chr11:73545008
|
C | T | 32 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(29): Show | 32 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.-19+52915G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545008 | ||||||
| chr11:73545009
|
T | A | 4 | a0001c0001t0010g0002a0001c0001t0022g0061a0001c0001t0022g0062others(1): Show | 4 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+52914A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545009 | ||||||
| chr11:73545010
|
A | ATATATAA others(169): Show |
1 | a0001c0001t0010g0001 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-19+52912_-19+5291 others(180): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545010 | ||||||
| chr11:73545010
|
A | T | 4 | a0001c0001t0010g0002a0001c0001t0022g0061a0001c0001t0022g0062others(1): Show | 4 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+52913T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545010 | ||||||
| chr11:73545013
|
T | TATAATAT others(103): Show |
1 | a0001c0003t0028g0064 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-19+52909_-19+5291 others(114): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545013 | ||||||
| chr11:73545013
|
T | TATAATAT others(78): Show |
1 | a0001c0003t0004g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-19+52909_-19+5291 others(89): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545013 | ||||||
| chr11:73545014
|
A | ATAATATA others(133): Show |
1 | a0001c0001t0039g0125 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-19+52908_-19+5290 others(144): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545014 | ||||||
| chr11:73545014
|
A | ATAATATA others(113): Show |
1 | a0001c0001t0040g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-19+52908_-19+5290 others(124): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545014 | ||||||
| chr11:73545015
|
T | TA | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+52907dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545015 | ||||||
| chr11:73545017
|
T | A | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+52906A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545017 | ||||||
| chr11:73545018
|
A | T | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+52905T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545018 | ||||||
| chr11:73545019
|
G | A | 84 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(81): Show | 84 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-19+52904C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545019 | ||||||
| chr11:73545019
|
G | T | 9 | a0001c0001t0010g0004a0001c0001t0017g0032a0001c0001t0017g0078others(6): Show | 9 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19+52904C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545019 | ||||||
| chr11:73545020
|
T | A | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+52903A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545020 | ||||||
| chr11:73545021
|
A | T | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+52902T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545021 | ||||||
| chr11:73545023
|
A | AT | 76 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-19+52899dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545023 | ||||||
| chr11:73545025
|
A | T | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+52898T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545025 | ||||||
| chr11:73545026
|
T | TTA | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+52896_-19+5289 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545026 | ||||||
| chr11:73545026
|
T | TTATATAT others(118): Show |
4 | a0001c0001t0010g0002a0001c0001t0022g0061a0001c0001t0022g0062others(1): Show | 4 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+52896_-19+5289 others(129): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545026 | ||||||
| chr11:73545027
|
A | AT | 50 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(47): Show | 50 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.-19+52895_-19+5289 others(5): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545027 | ||||||
| chr11:73545027
|
A | ATAATATA others(32): Show |
26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+52895_-19+5289 others(43): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545027 | ||||||
| chr11:73545027
|
A | ATAT | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19+52895_-19+5289 others(7): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545027 | ||||||
| chr11:73545027
|
A | T | 8 | a0001c0001t0010g0002a0001c0001t0019g0069a0001c0001t0019g0070others(5): Show | 8 | HG01106.hp2 HG01884.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+52896T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545027 | ||||||
| chr11:73545038
|
A | ATAATATA others(30): Show |
2 | a0001c0001t0017g0032a0001c0001t0017g0078 | 2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-19+52884_-19+5288 others(41): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545038 | ||||||
| chr11:73545038
|
A | ATAATATA others(30): Show |
2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-19+52884_-19+5288 others(41): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545038 | ||||||
| chr11:73545041
|
T | A | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52882A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545041 | ||||||
| chr11:73545043
|
T | A | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52880A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545043 | ||||||
| chr11:73545045
|
G | A | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52878C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545045 | ||||||
| chr11:73545046
|
G | T | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52877C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545046 | ||||||
| chr11:73545048
|
G | A | 1 | a0001c0001t0022g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-19+52875C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545048 | ||||||
| chr11:73545048
|
G | T | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52875C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545048 | ||||||
| chr11:73545052
|
G | T | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52871C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545052 | ||||||
| chr11:73545054
|
C | A | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52869G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545054 | ||||||
| chr11:73545056
|
C | A | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52867G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545056 | ||||||
| chr11:73545057
|
C | T | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52866G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545057 | ||||||
| chr11:73545058
|
C | A | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52865G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545058 | ||||||
| chr11:73545060
|
C | A | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52863G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545060 | ||||||
| chr11:73545062
|
G | A | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52861C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545062 | ||||||
| chr11:73545067
|
C | A | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52856G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545067 | ||||||
| chr11:73545068
|
C | T | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52855G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545068 | ||||||
| chr11:73545069
|
A | AATTATAT others(4): Show |
1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52853_-19+5285 others(15): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545069 | ||||||
| chr11:73545070
|
G | A | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52853C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545070 | ||||||
| chr11:73545071
|
G | T | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52852C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545071 | ||||||
| chr11:73545072
|
C | A | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52851G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545072 | ||||||
| chr11:73545075
|
G | T | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52848C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545075 | ||||||
| chr11:73545083
|
C | A | 1 | a0001c0001t0010g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+52840G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545083 | ||||||
| chr11:73545084
|
G | A | 1 | a0001c0002t0005g0059 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-19+52839C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545084 | ||||||
| chr11:73545227
|
T | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+52696A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545227 | ||||||
| chr11:73545483
|
C | T | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-19+52440G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545483 | ||||||
| chr11:73545612
|
G | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+52311C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545612 | ||||||
| chr11:73545683
|
C | CT | 17 | a0001c0001t0002g0007a0001c0001t0002g0013a0001c0001t0006g0067others(14): Show | 17 | HG01109.hp1 HG01109.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.-19+52239dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545683 | ||||||
| chr11:73545683
|
C | CTT | 23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-19+52238_-19+5223 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545683 | ||||||
| chr11:73545683
|
C | CTTT | 5 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(2): Show | 5 | HG02818.hp2 NA18965.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+52237_-19+5223 others(7): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545683 | ||||||
| chr11:73545683
|
CT | C | 19 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(16): Show | 19 | HG01167.hp1 HG01884.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.-19+52239delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545683 | ||||||
| chr11:73545752
|
C | T | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+52171G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545752 | ||||||
| chr11:73545829
|
A | G | 34 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(31): Show | 34 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+52094T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545829 | ||||||
| chr11:73545837
|
C | T | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+52086G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73545837 | ||||||
| chr11:73546009
|
C | G | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+51914G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73546009 | ||||||
| chr11:73546343
|
A | G | 1 | a0001c0002t0001g0042 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-19+51580T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73546343 | ||||||
| chr11:73546495
|
G | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+51428C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73546495 | ||||||
| chr11:73546645
|
T | C | 2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-19+51278A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73546645 | ||||||
| chr11:73546732
|
C | CA | 25 | a0001c0001t0002g0019a0001c0001t0003g0158a0001c0001t0003g0160others(22): Show | 25 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.-19+51190dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73546732 | ||||||
| chr11:73546732
|
CA | C | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-19+51190delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73546732 | ||||||
| chr11:73546876
|
G | A | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19+51047C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73546876 | ||||||
| chr11:73547085
|
G | GA | 8 | a0001c0001t0004g0145a0001c0001t0017g0032a0001c0001t0017g0078others(5): Show | 8 | HG01433.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+50837dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73547085 | ||||||
| chr11:73547085
|
GA | G | 5 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0025g0120others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+50837delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73547085 | ||||||
| chr11:73547184
|
G | A | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+50739C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73547184 | ||||||
| chr11:73547393
|
T | C | 1 | a0001c0002t0005g0085 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-19+50530A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73547393 | ||||||
| chr11:73547421
|
G | T | 1 | a0001c0001t0019g0070 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-19+50502C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73547421 | ||||||
| chr11:73547444
|
A | T | 1 | a0001c0001t0019g0070 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-19+50479T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73547444 | ||||||
| chr11:73547846
|
T | C | 1 | a0001c0002t0005g0085 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-19+50077A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73547846 | ||||||
| chr11:73547850
|
G | GA | 26 | a0001c0001t0002g0013a0001c0001t0004g0138a0001c0001t0004g0139others(23): Show | 26 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+50072dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73547850 | ||||||
| chr11:73547850
|
GA | G | 5 | a0001c0001t0017g0078a0001c0001t0018g0128a0001c0001t0018g0130others(2): Show | 5 | HG00438.hp2 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+50072delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73547850 | ||||||
| chr11:73547867
|
A | G | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+50056T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73547867 | ||||||
| chr11:73547967
|
G | T | 26 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(23): Show | 26 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+49956C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73547967 | ||||||
| chr11:73548209
|
G | C | 1 | a0001c0001t0003g0158 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-19+49714C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73548209 | ||||||
| chr11:73548248
|
T | C | 2 | a0001c0002t0020g0109a0001c0002t0023g0107 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-19+49675A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73548248 | ||||||
| chr11:73548278
|
G | A | 4 | a0001c0002t0001g0071a0001c0002t0001g0121a0001c0002t0001g0122others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+49645C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73548278 | ||||||
| chr11:73548332
|
AT | A | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-19+49590delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73548332 | ||||||
| chr11:73548498
|
A | C | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+49425T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73548498 | ||||||
| chr11:73548522
|
A | C | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19+49401T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73548522 | ||||||
| chr11:73548649
|
T | G | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-19+49274A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73548649 | ||||||
| chr11:73548651
|
G | T | 2 | a0001c0002t0001g0034a0001c0002t0001g0080 | 2 | HG01257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-19+49272C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73548651 | ||||||
| chr11:73548918
|
G | C | 5 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0025g0120others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+49005C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73548918 | ||||||
| chr11:73548964
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-19+48959G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73548964 | ||||||
| chr11:73549001
|
G | A | 26 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(23): Show | 26 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+48922C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73549001 | ||||||
| chr11:73549314
|
T | C | 3 | a0001c0002t0001g0088a0001c0002t0001g0089a0001c0002t0001g0091 | 3 | HG02622.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-19+48609A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73549314 | ||||||
| chr11:73549418
|
A | C | 62 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 62 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(59): Show |
intron_variant | MODIFIER | c.-19+48505T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73549418 | ||||||
| chr11:73549673
|
C | T | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+48250G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73549673 | ||||||
| chr11:73549798
|
A | G | 1 | a0001c0002t0001g0034 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-19+48125T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73549798 | ||||||
| chr11:73550241
|
A | T | 23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-19+47682T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73550241 | ||||||
| chr11:73550298
|
G | A | 1 | a0001c0002t0001g0038 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-19+47625C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73550298 | ||||||
| chr11:73550379
|
C | G | 26 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(23): Show | 26 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+47544G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73550379 | ||||||
| chr11:73550422
|
A | C | 26 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(23): Show | 26 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+47501T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73550422 | ||||||
| chr11:73550491
|
T | C | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19+47432A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73550491 | ||||||
| chr11:73550576
|
G | A | 1 | a0001c0002t0005g0155 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-19+47347C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73550576 | ||||||
| chr11:73550689
|
T | C | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+47234A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73550689 | ||||||
| chr11:73550902
|
T | C | 3 | a0001c0001t0003g0162a0001c0001t0003g0167a0001c0001t0003g0176 | 3 | HG00544.hp2 HG01978.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-19+47021A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73550902 | ||||||
| chr11:73551068
|
G | A | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+46855C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73551068 | ||||||
| chr11:73551110
|
CA | C | 11 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(8): Show | 11 | HG01106.hp2 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+46812delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73551110 | ||||||
| chr11:73551110
|
CAA | C | 17 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(14): Show | 17 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.-19+46811_-19+4681 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73551110 | ||||||
| chr11:73551158
|
C | T | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-19+46765G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73551158 | ||||||
| chr11:73551549
|
A | G | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+46374T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73551549 | ||||||
| chr11:73551587
|
T | C | 3 | a0001c0001t0016g0135a0001c0001t0016g0136a0001c0001t0041g0134 | 3 | HG02615.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-19+46336A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73551587 | ||||||
| chr11:73551626
|
C | G | 4 | a0001c0002t0001g0071a0001c0002t0001g0121a0001c0002t0001g0122others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+46297G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73551626 | ||||||
| chr11:73552002
|
G | A | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+45921C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73552002 | ||||||
| chr11:73552363
|
A | G | 1 | a0001c0001t0014g0154 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-19+45560T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73552363 | ||||||
| chr11:73552398
|
C | T | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-19+45525G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73552398 | ||||||
| chr11:73552705
|
T | G | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-19+45218A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73552705 | ||||||
| chr11:73552967
|
T | C | 1 | a0001c0002t0001g0115 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-19+44956A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73552967 | ||||||
| chr11:73552995
|
G | A | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+44928C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73552995 | ||||||
| chr11:73553131
|
A | G | 1 | a0001c0001t0006g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-19+44792T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73553131 | ||||||
| chr11:73553174
|
G | C | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+44749C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73553174 | ||||||
| chr11:73553461
|
G | C | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+44462C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73553461 | ||||||
| chr11:73553505
|
G | A | 2 | a0001c0001t0022g0061a0001c0001t0022g0062 | 2 | HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-19+44418C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73553505 | ||||||
| chr11:73553611
|
C | T | 60 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(57): Show | 60 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.-19+44312G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73553611 | ||||||
| chr11:73553632
|
T | C | 1 | a0001c0001t0043g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-19+44291A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73553632 | ||||||
| chr11:73553647
|
T | A | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-19+44276A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73553647 | ||||||
| chr11:73553710
|
A | G | 34 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(31): Show | 34 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.-19+44213T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73553710 | ||||||
| chr11:73553742
|
G | T | 2 | a0001c0002t0013g0101a0001c0002t0013g0102 | 2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-19+44181C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73553742 | ||||||
| chr11:73554102
|
G | A | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+43821C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73554102 | ||||||
| chr11:73554162
|
G | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+43761C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73554162 | ||||||
| chr11:73554251
|
G | A | 1 | a0001c0002t0021g0054 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-19+43672C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73554251 | ||||||
| chr11:73554600
|
G | C | 1 | a0001c0002t0009g0076 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-19+43323C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73554600 | ||||||
| chr11:73554935
|
T | G | 1 | a0001c0002t0001g0031 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-19+42988A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73554935 | ||||||
| chr11:73554956
|
T | C | 1 | a0001c0002t0001g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-19+42967A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73554956 | ||||||
| chr11:73554960
|
G | A | 30 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(27): Show | 30 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19+42963C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73554960 | ||||||
| chr11:73555026
|
C | G | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+42897G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73555026 | ||||||
| chr11:73555064
|
T | C | 1 | a0001c0002t0005g0085 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-19+42859A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73555064 | ||||||
| chr11:73555309
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-19+42614C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73555309 | ||||||
| chr11:73555581
|
G | A | 1 | a0001c0001t0017g0078 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-19+42342C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73555581 | ||||||
| chr11:73555640
|
A | G | 1 | a0001c0002t0001g0119 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-19+42283T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73555640 | ||||||
| chr11:73555814
|
C | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+42109G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73555814 | ||||||
| chr11:73556072
|
A | G | 2 | a0001c0002t0046g0100a0001c0002t0047g0114 | 2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-19+41851T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73556072 | ||||||
| chr11:73556128
|
T | TG | 179 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-19+41794dupC | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73556128 | ||||||
| chr11:73556146
|
A | C | 179 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-19+41777T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73556146 | ||||||
| chr11:73556153
|
G | C | 4 | a0001c0002t0001g0071a0001c0002t0001g0121a0001c0002t0001g0122others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+41770C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73556153 | ||||||
| chr11:73556161
|
TA | T | 179 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-19+41761delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73556161 | ||||||
| chr11:73556175
|
G | T | 179 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-19+41748C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73556175 | ||||||
| chr11:73556182
|
C | A | 179 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-19+41741G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73556182 | ||||||
| chr11:73556259
|
G | A | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+41664C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73556259 | ||||||
| chr11:73556415
|
A | G | 1 | a0001c0002t0001g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-19+41508T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73556415 | ||||||
| chr11:73556866
|
A | C | 1 | a0001c0001t0007g0026 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-19+41057T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73556866 | ||||||
| chr11:73557028
|
C | CA | 18 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-19+40894dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73557028 | ||||||
| chr11:73557623
|
T | C | 2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+40300A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73557623 | ||||||
| chr11:73557866
|
A | G | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-19+40057T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73557866 | ||||||
| chr11:73557964
|
T | C | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+39959A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73557964 | ||||||
| chr11:73558177
|
G | A | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-19+39746C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73558177 | ||||||
| chr11:73558307
|
T | G | 1 | a0001c0001t0002g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-19+39616A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73558307 | ||||||
| chr11:73558337
|
T | C | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+39586A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73558337 | ||||||
| chr11:73558463
|
T | C | 1 | a0001c0002t0001g0057 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-19+39460A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73558463 | ||||||
| chr11:73558469
|
T | TA | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+39453dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73558469 | ||||||
| chr11:73558469
|
TA | T | 22 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(19): Show | 22 | HG00140.hp2 HG01168.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+39453delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73558469 | ||||||
| chr11:73558469
|
TAA | T | 7 | a0001c0001t0007g0023a0001c0001t0019g0069a0001c0001t0019g0070others(4): Show | 7 | HG01106.hp2 HG01167.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+39452_-19+3945 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73558469 | ||||||
| chr11:73558469
|
TAAA | T | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+39451_-19+3945 others(7): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73558469 | ||||||
| chr11:73558516
|
A | T | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+39407T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73558516 | ||||||
| chr11:73558561
|
C | T | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+39362G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73558561 | ||||||
| chr11:73558616
|
A | AC | 2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+39306_-19+3930 others(5): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73558616 | ||||||
| chr11:73558617
|
T | A | 2 | a0001c0001t0014g0153a0001c0001t0014g0154 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-19+39306A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73558617 | ||||||
| chr11:73558771
|
T | C | 1 | a0001c0001t0004g0147 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-19+39152A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73558771 | ||||||
| chr11:73559027
|
T | C | 3 | a0001c0001t0016g0135a0001c0001t0016g0136a0001c0001t0041g0134 | 3 | HG02615.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-19+38896A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73559027 | ||||||
| chr11:73559162
|
C | G | 1 | a0001c0002t0009g0073 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-19+38761G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73559162 | ||||||
| chr11:73559420
|
T | G | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19+38503A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73559420 | ||||||
| chr11:73559431
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-19+38492G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73559431 | ||||||
| chr11:73559432
|
G | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+38491C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73559432 | ||||||
| chr11:73560007
|
C | G | 1 | a0001c0002t0009g0073 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-19+37916G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73560007 | ||||||
| chr11:73560109
|
G | T | 1 | a0001c0002t0009g0073 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-19+37814C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73560109 | ||||||
| chr11:73560110
|
C | T | 1 | a0001c0002t0009g0073 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-19+37813G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73560110 | ||||||
| chr11:73560142
|
C | T | 1 | a0001c0002t0001g0097 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-19+37781G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73560142 | ||||||
| chr11:73560188
|
T | C | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-19+37735A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73560188 | ||||||
| chr11:73560278
|
G | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+37645C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73560278 | ||||||
| chr11:73560290
|
T | C | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+37633A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73560290 | ||||||
| chr11:73560398
|
T | C | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+37525A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73560398 | ||||||
| chr11:73560943
|
T | C | 60 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(57): Show | 60 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.-19+36980A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73560943 | ||||||
| chr11:73561018
|
C | T | 1 | a0001c0002t0047g0114 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-19+36905G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561018 | ||||||
| chr11:73561071
|
AAAC | A | 10 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+36849_-19+3685 others(7): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561071 | ||||||
| chr11:73561072
|
AAC | A | 31 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(28): Show | 31 | HG01106.hp2 HG01884.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.-19+36849_-19+3685 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561072 | ||||||
| chr11:73561073
|
AC | A | 44 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(41): Show | 44 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.-19+36849delG | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561073 | ||||||
| chr11:73561074
|
C | A | 8 | a0001c0001t0003g0162a0001c0001t0003g0166a0001c0001t0003g0170others(5): Show | 8 | HG01978.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+36849G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561074 | ||||||
| chr11:73561081
|
C | A | 16 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(13): Show | 16 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+36842G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561081 | ||||||
| chr11:73561090
|
C | T | 28 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(25): Show | 28 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.-19+36833G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561090 | ||||||
| chr11:73561095
|
G | A | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-19+36828C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561095 | ||||||
| chr11:73561122
|
C | T | 1 | a0001c0001t0052g0157 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-19+36801G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561122 | ||||||
| chr11:73561146
|
A | G | 62 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 62 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(59): Show |
intron_variant | MODIFIER | c.-19+36777T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561146 | ||||||
| chr11:73561165
|
G | A | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-19+36758C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561165 | ||||||
| chr11:73561190
|
C | T | 2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-19+36733G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561190 | ||||||
| chr11:73561194
|
G | C | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+36729C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561194 | ||||||
| chr11:73561331
|
C | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+36592G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561331 | ||||||
| chr11:73561462
|
C | CAT | 11 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(8): Show | 11 | HG01106.hp2 HG01884.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+36459_-19+3646 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561462 | ||||||
| chr11:73561543
|
A | C | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19+36380T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561543 | ||||||
| chr11:73561656
|
T | C | 1 | a0001c0002t0001g0046 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-19+36267A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561656 | ||||||
| chr11:73561901
|
T | G | 62 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(59): Show | 62 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(59): Show |
intron_variant | MODIFIER | c.-19+36022A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561901 | ||||||
| chr11:73561902
|
C | T | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+36021G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561902 | ||||||
| chr11:73561957
|
T | C | 1 | a0001c0002t0005g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-19+35966A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561957 | ||||||
| chr11:73561963
|
G | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+35960C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561963 | ||||||
| chr11:73561986
|
A | G | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+35937T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73561986 | ||||||
| chr11:73562054
|
T | G | 10 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+35869A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73562054 | ||||||
| chr11:73562131
|
T | C | 1 | a0001c0002t0046g0100 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-19+35792A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73562131 | ||||||
| chr11:73562231
|
G | A | 16 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(13): Show | 16 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19+35692C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73562231 | ||||||
| chr11:73562327
|
G | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+35596C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73562327 | ||||||
| chr11:73562437
|
AGT | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+35484_-19+3548 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73562437 | ||||||
| chr11:73562469
|
G | T | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+35454C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73562469 | ||||||
| chr11:73562638
|
C | T | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+35285G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73562638 | ||||||
| chr11:73562825
|
C | CA | 23 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(20): Show | 23 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-19+35097dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73562825 | ||||||
| chr11:73563381
|
T | C | 2 | a0001c0001t0004g0147a0001c0001t0027g0146 | 2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-19+34542A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73563381 | ||||||
| chr11:73563415
|
C | T | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-19+34508G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73563415 | ||||||
| chr11:73563425
|
A | T | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-19+34498T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73563425 | ||||||
| chr11:73563463
|
C | T | 2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-19+34460G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73563463 | ||||||
| chr11:73563491
|
G | T | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+34432C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73563491 | ||||||
| chr11:73563508
|
A | G | 1 | a0001c0001t0037g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-19+34415T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73563508 | ||||||
| chr11:73563771
|
T | C | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19+34152A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73563771 | ||||||
| chr11:73563787
|
C | T | 30 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(27): Show | 30 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19+34136G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73563787 | ||||||
| chr11:73563829
|
T | C | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+34094A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73563829 | ||||||
| chr11:73563930
|
G | C | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+33993C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73563930 | ||||||
| chr11:73564131
|
A | G | 16 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(13): Show | 16 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+33792T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73564131 | ||||||
| chr11:73564351
|
A | G | 1 | a0001c0002t0001g0036 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-19+33572T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73564351 | ||||||
| chr11:73564742
|
C | CA | 18 | a0001c0001t0002g0014a0001c0001t0004g0137a0001c0001t0004g0138others(15): Show | 18 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-19+33180dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73564742 | ||||||
| chr11:73564856
|
A | T | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+33067T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73564856 | ||||||
| chr11:73564865
|
G | GA | 10 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+33057dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73564865 | ||||||
| chr11:73564905
|
T | G | 2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-19+33018A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73564905 | ||||||
| chr11:73565237
|
G | A | 1 | a0001c0001t0052g0157 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-19+32686C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73565237 | ||||||
| chr11:73565288
|
A | G | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+32635T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73565288 | ||||||
| chr11:73565310
|
G | A | 1 | a0002c0005t0001g0055 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-19+32613C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73565310 | ||||||
| chr11:73565588
|
C | CAAGATAA others(310): Show |
15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+32334_-19+3233 others(321): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73565588 | ||||||
| chr11:73565683
|
T | C | 7 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(4): Show | 7 | HG02055.hp2 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+32240A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73565683 | ||||||
| chr11:73565855
|
C | T | 91 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(88): Show | 91 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.-19+32068G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73565855 | ||||||
| chr11:73566237
|
T | C | 2 | a0001c0001t0025g0120a0001c0002t0001g0086 | 2 | NA19084.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-19+31686A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73566237 | ||||||
| chr11:73566489
|
A | G | 7 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(4): Show | 7 | HG02055.hp2 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+31434T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73566489 | ||||||
| chr11:73566554
|
T | C | 6 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(3): Show | 6 | HG02258.hp2 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+31369A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73566554 | ||||||
| chr11:73566695
|
C | G | 3 | a0001c0001t0016g0135a0001c0001t0016g0136a0001c0001t0041g0134 | 3 | HG02615.hp1 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-19+31228G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73566695 | ||||||
| chr11:73566930
|
A | C | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+30993T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73566930 | ||||||
| chr11:73567023
|
C | T | 4 | a0001c0002t0001g0071a0001c0002t0001g0121a0001c0002t0001g0122others(1): Show | 4 | HG02145.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+30900G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73567023 | ||||||
| chr11:73567269
|
G | A | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-19+30654C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73567269 | ||||||
| chr11:73567488
|
A | T | 1 | a0001c0002t0005g0155 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-19+30435T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73567488 | ||||||
| chr11:73567577
|
A | G | 1 | a0001c0002t0001g0029 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-19+30346T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73567577 | ||||||
| chr11:73567859
|
C | G | 1 | a0001c0001t0014g0153 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-19+30064G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73567859 | ||||||
| chr11:73568006
|
C | CT | 3 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0028 | 3 | HG02451.hp1 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-19+29916dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73568006 | ||||||
| chr11:73568251
|
C | T | 92 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(89): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-19+29672G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73568251 | ||||||
| chr11:73568258
|
C | T | 4 | a0001c0001t0004g0142a0001c0001t0004g0143a0001c0001t0026g0144others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+29665G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73568258 | ||||||
| chr11:73568350
|
G | A | 1 | a0001c0003t0028g0064 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-19+29573C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73568350 | ||||||
| chr11:73568381
|
T | G | 24 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(21): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+29542A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73568381 | ||||||
| chr11:73568499
|
C | T | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+29424G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73568499 | ||||||
| chr11:73568690
|
T | A | 24 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(21): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+29233A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73568690 | ||||||
| chr11:73568723
|
C | G | 1 | a0001c0001t0003g0167 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-19+29200G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73568723 | ||||||
| chr11:73568724
|
G | A | 1 | a0001c0001t0018g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-19+29199C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73568724 | ||||||
| chr11:73568811
|
C | T | 25 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(22): Show | 25 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.-19+29112G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73568811 | ||||||
| chr11:73569341
|
A | T | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+28582T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73569341 | ||||||
| chr11:73569535
|
A | T | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+28388T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73569535 | ||||||
| chr11:73569561
|
T | A | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+28362A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73569561 | ||||||
| chr11:73569605
|
C | T | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-19+28318G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73569605 | ||||||
| chr11:73569683
|
G | A | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+28240C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73569683 | ||||||
| chr11:73569825
|
A | AAAAT | 4 | a0001c0002t0001g0034a0001c0002t0005g0047a0001c0002t0013g0101others(1): Show | 4 | HG01257.hp1 HG01928.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+28094_-19+2809 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73569825 | ||||||
| chr11:73569825
|
A | AAAATAAA others(1): Show |
9 | a0001c0001t0016g0135a0001c0001t0016g0136a0001c0001t0017g0032others(6): Show | 9 | HG02055.hp1 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19+28090_-19+2809 others(12): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73569825 | ||||||
| chr11:73569825
|
A | AAAATAAA others(5): Show |
27 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(24): Show | 27 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.-19+28086_-19+2809 others(16): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73569825 | ||||||
| chr11:73569825
|
A | AAAATAAA others(9): Show |
7 | a0001c0001t0003g0163a0001c0001t0003g0164a0001c0001t0003g0165others(4): Show | 7 | HG01167.hp2 HG01934.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+28082_-19+2809 others(20): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73569825 | ||||||
| chr11:73569825
|
AAAAT | A | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+28094_-19+2809 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73569825 | ||||||
| chr11:73569825
|
AAAATAAA others(5): Show |
A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+28086_-19+2809 others(16): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73569825 | ||||||
| chr11:73569853
|
TAAATAAA others(1): Show |
T | 16 | a0001c0001t0004g0145a0001c0001t0004g0147a0001c0001t0004g0151others(13): Show | 16 | HG02109.hp2 HG02258.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+28062_-19+2806 others(12): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73569853 | ||||||
| chr11:73569857
|
TAAAC | T | 8 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+28062_-19+2806 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73569857 | ||||||
| chr11:73569910
|
GA | G | 56 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(53): Show | 56 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(53): Show |
intron_variant | MODIFIER | c.-19+28012delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73569910 | ||||||
| chr11:73569991
|
G | A | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-19+27932C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73569991 | ||||||
| chr11:73570011
|
T | C | 1 | a0001c0002t0001g0042 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-19+27912A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73570011 | ||||||
| chr11:73570077
|
AAG | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+27844_-19+2784 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73570077 | ||||||
| chr11:73570098
|
G | A | 24 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(21): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+27825C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73570098 | ||||||
| chr11:73570300
|
G | A | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+27623C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73570300 | ||||||
| chr11:73570539
|
T | C | 24 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(21): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+27384A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73570539 | ||||||
| chr11:73570597
|
G | C | 1 | a0001c0002t0001g0097 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-19+27326C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73570597 | ||||||
| chr11:73570733
|
C | CA | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+27189dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73570733 | ||||||
| chr11:73570875
|
G | A | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+27048C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73570875 | ||||||
| chr11:73570934
|
C | A | 1 | a0001c0002t0001g0090 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-19+26989G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73570934 | ||||||
| chr11:73571097
|
C | A | 4 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(1): Show | 4 | NA18965.hp1 NA18981.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+26826G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571097 | ||||||
| chr11:73571193
|
CA | C | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+26729delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571193 | ||||||
| chr11:73571234
|
T | C | 1 | a0001c0002t0012g0113 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-19+26689A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571234 | ||||||
| chr11:73571234
|
T | TC | 50 | a0001c0001t0003g0176a0001c0001t0017g0032a0001c0002t0001g0029others(47): Show | 50 | HG00140.hp1 HG00438.hp2 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.-19+26688dupG | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571234 | ||||||
| chr11:73571234
|
T | TCC | 13 | a0001c0001t0008g0175a0001c0001t0052g0157a0001c0002t0001g0033others(10): Show | 13 | HG01109.hp2 HG01167.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+26687_-19+2668 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571234 | ||||||
| chr11:73571234
|
TC | T | 15 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(12): Show | 15 | HG00323.hp1 HG01106.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+26688delG | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571234 | ||||||
| chr11:73571237
|
C | CCCT | 18 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(15): Show | 18 | HG01884.hp1 HG02109.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.-19+26685_-19+2668 others(7): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571237 | ||||||
| chr11:73571241
|
C | G | 1 | a0001c0006t0001g0083 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-19+26682G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571241 | ||||||
| chr11:73571243
|
C | CCCT | 16 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(13): Show | 16 | HG01255.hp2 HG01934.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+26679_-19+2668 others(7): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571243 | ||||||
| chr11:73571243
|
C | T | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+26680G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571243 | ||||||
| chr11:73571245
|
T | C | 2 | a0001c0002t0001g0039a0001c0002t0005g0050 | 2 | HG02683.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-19+26678A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571245 | ||||||
| chr11:73571264
|
C | CCTCTCT | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+26653_-19+2665 others(10): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571264 | ||||||
| chr11:73571294
|
G | C | 2 | a0001c0002t0046g0100a0001c0002t0047g0114 | 2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-19+26629C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571294 | ||||||
| chr11:73571354
|
C | T | 20 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(17): Show | 20 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-19+26569G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571354 | ||||||
| chr11:73571360
|
C | CG | 5 | a0001c0002t0001g0029a0001c0002t0005g0047a0001c0002t0005g0048others(2): Show | 5 | HG01069.hp2 HG01928.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+26562_-19+2656 others(5): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571360 | ||||||
| chr11:73571361
|
T | A | 5 | a0001c0002t0001g0029a0001c0002t0005g0047a0001c0002t0005g0048others(2): Show | 5 | HG01069.hp2 HG01928.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+26562A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571361 | ||||||
| chr11:73571362
|
C | G | 5 | a0001c0002t0001g0029a0001c0002t0005g0047a0001c0002t0005g0048others(2): Show | 5 | HG01069.hp2 HG01928.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+26561G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571362 | ||||||
| chr11:73571363
|
A | T | 5 | a0001c0002t0001g0029a0001c0002t0005g0047a0001c0002t0005g0048others(2): Show | 5 | HG01069.hp2 HG01928.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+26560T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571363 | ||||||
| chr11:73571381
|
G | A | 1 | a0001c0002t0001g0065 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-19+26542C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571381 | ||||||
| chr11:73571401
|
A | G | 1 | a0001c0002t0012g0082 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-19+26522T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571401 | ||||||
| chr11:73571669
|
C | T | 1 | a0001c0002t0001g0091 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19+26254G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571669 | ||||||
| chr11:73571881
|
C | A | 1 | a0001c0001t0043g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-19+26042G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571881 | ||||||
| chr11:73571903
|
C | G | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+26020G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571903 | ||||||
| chr11:73571926
|
C | T | 16 | a0001c0001t0003g0176a0001c0002t0001g0075a0001c0002t0001g0106others(13): Show | 16 | HG00140.hp1 HG00323.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19+25997G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571926 | ||||||
| chr11:73571967
|
G | A | 10 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+25956C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571967 | ||||||
| chr11:73571982
|
C | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+25941G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571982 | ||||||
| chr11:73571985
|
C | T | 7 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(4): Show | 7 | HG01255.hp1 HG01257.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+25938G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571985 | ||||||
| chr11:73571990
|
G | A | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-19+25933C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73571990 | ||||||
| chr11:73572031
|
AGAAGTGA others(33): Show |
A | 1 | a0001c0003t0028g0064 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-19+25852_-19+2589 others(44): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572031 | ||||||
| chr11:73572043
|
C | A | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+25880G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572043 | ||||||
| chr11:73572054
|
G | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+25869C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572054 | ||||||
| chr11:73572090
|
G | A | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+25833C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572090 | ||||||
| chr11:73572145
|
C | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+25778G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572145 | ||||||
| chr11:73572179
|
G | A | 11 | a0001c0001t0004g0142a0001c0001t0004g0143a0001c0001t0004g0145others(8): Show | 11 | HG01168.hp2 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+25744C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572179 | ||||||
| chr11:73572182
|
C | T | 1 | a0001c0001t0017g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-19+25741G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572182 | ||||||
| chr11:73572186
|
C | T | 20 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(17): Show | 20 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-19+25737G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572186 | ||||||
| chr11:73572207
|
C | G | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19+25716G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572207 | ||||||
| chr11:73572208
|
A | G | 1 | a0001c0002t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-19+25715T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572208 | ||||||
| chr11:73572239
|
G | A | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+25684C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572239 | ||||||
| chr11:73572242
|
C | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+25681G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572242 | ||||||
| chr11:73572273
|
G | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+25650C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572273 | ||||||
| chr11:73572318
|
G | A | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+25605C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572318 | ||||||
| chr11:73572351
|
A | G | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-19+25572T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572351 | ||||||
| chr11:73572363
|
G | A | 9 | a0001c0001t0008g0159a0001c0001t0008g0172a0001c0001t0008g0173others(6): Show | 9 | HG00323.hp1 HG01168.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19+25560C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572363 | ||||||
| chr11:73572551
|
G | C | 1 | a0001c0002t0001g0097 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-19+25372C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572551 | ||||||
| chr11:73572638
|
G | A | 25 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(22): Show | 25 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.-19+25285C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572638 | ||||||
| chr11:73572747
|
A | G | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+25176T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572747 | ||||||
| chr11:73572873
|
A | AAAAT | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+25046_-19+2504 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572873 | ||||||
| chr11:73572892
|
A | T | 30 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(27): Show | 30 | HG00140.hp2 HG01109.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19+25031T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572892 | ||||||
| chr11:73572896
|
T | A | 105 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(102): Show | 105 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-19+25027A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572896 | ||||||
| chr11:73572945
|
T | A | 60 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(57): Show | 60 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.-19+24978A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572945 | ||||||
| chr11:73572954
|
A | G | 1 | a0001c0002t0001g0044 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-19+24969T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73572954 | ||||||
| chr11:73573040
|
G | A | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+24883C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73573040 | ||||||
| chr11:73573070
|
C | T | 1 | a0001c0002t0001g0065 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-19+24853G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73573070 | ||||||
| chr11:73573130
|
T | C | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+24793A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73573130 | ||||||
| chr11:73573188
|
G | A | 1 | a0001c0002t0001g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-19+24735C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73573188 | ||||||
| chr11:73573439
|
C | A | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+24484G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73573439 | ||||||
| chr11:73573499
|
T | C | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+24424A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73573499 | ||||||
| chr11:73573558
|
C | T | 1 | a0001c0002t0009g0073 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-19+24365G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73573558 | ||||||
| chr11:73573686
|
C | T | 1 | a0001c0001t0006g0180 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-19+24237G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73573686 | ||||||
| chr11:73573756
|
G | A | 1 | a0001c0002t0001g0091 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19+24167C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73573756 | ||||||
| chr11:73573761
|
C | T | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-19+24162G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73573761 | ||||||
| chr11:73573891
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-19+24032C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73573891 | ||||||
| chr11:73573949
|
G | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+23974C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73573949 | ||||||
| chr11:73574019
|
G | A | 1 | a0001c0001t0022g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-19+23904C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73574019 | ||||||
| chr11:73574084
|
CTG | C | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+23837_-19+2383 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73574084 | ||||||
| chr11:73574094
|
G | A | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+23829C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73574094 | ||||||
| chr11:73574476
|
T | C | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+23447A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73574476 | ||||||
| chr11:73574565
|
G | T | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+23358C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73574565 | ||||||
| chr11:73574710
|
C | T | 1 | a0001c0002t0001g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-19+23213G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73574710 | ||||||
| chr11:73574718
|
AT | A | 119 | a0001c0001t0002g0018a0001c0001t0003g0160a0001c0001t0003g0161others(116): Show | 119 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-19+23204delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73574718 | ||||||
| chr11:73574718
|
ATTTT | A | 14 | a0001c0001t0004g0142a0001c0001t0004g0143a0001c0001t0004g0145others(11): Show | 14 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19+23201_-19+2320 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73574718 | ||||||
| chr11:73574742
|
T | G | 2 | a0001c0001t0018g0128a0001c0001t0018g0130 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-19+23181A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73574742 | ||||||
| chr11:73574921
|
CCT | C | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+23000_-19+2300 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73574921 | ||||||
| chr11:73574969
|
A | ATTACTGA others(12): Show |
60 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(57): Show | 60 | HG00140.hp2 HG01106.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.-19+22953_-19+2295 others(23): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73574969 | ||||||
| chr11:73575095
|
G | A | 1 | a0001c0002t0021g0054 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-19+22828C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73575095 | ||||||
| chr11:73575331
|
T | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+22592A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73575331 | ||||||
| chr11:73575426
|
T | C | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+22497A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73575426 | ||||||
| chr11:73575514
|
C | T | 4 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0001g0095others(1): Show | 4 | HG02145.hp1 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+22409G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73575514 | ||||||
| chr11:73575534
|
G | T | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+22389C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73575534 | ||||||
| chr11:73575592
|
G | A | 10 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+22331C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73575592 | ||||||
| chr11:73575687
|
T | G | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+22236A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73575687 | ||||||
| chr11:73575867
|
CA | C | 26 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(23): Show | 26 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+22055delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73575867 | ||||||
| chr11:73576095
|
G | C | 10 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+21828C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73576095 | ||||||
| chr11:73576377
|
G | A | 1 | a0001c0001t0011g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-19+21546C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73576377 | ||||||
| chr11:73576673
|
T | C | 6 | a0001c0001t0011g0149a0001c0001t0011g0150a0001c0001t0017g0032others(3): Show | 6 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+21250A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73576673 | ||||||
| chr11:73576702
|
A | G | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+21221T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73576702 | ||||||
| chr11:73576840
|
G | A | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-19+21083C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73576840 | ||||||
| chr11:73576953
|
TA | T | 87 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(84): Show | 87 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-19+20969delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73576953 | ||||||
| chr11:73576954
|
A | T | 1 | a0001c0002t0009g0073 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-19+20969T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73576954 | ||||||
| chr11:73577167
|
G | A | 20 | a0001c0001t0004g0142a0001c0001t0004g0143a0001c0001t0004g0145others(17): Show | 20 | HG02109.hp2 HG02258.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.-19+20756C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73577167 | ||||||
| chr11:73577229
|
C | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+20694G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73577229 | ||||||
| chr11:73577312
|
C | A | 1 | a0001c0002t0001g0097 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-19+20611G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73577312 | ||||||
| chr11:73577319
|
TTAAC | T | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+20600_-19+2060 others(8): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73577319 | ||||||
| chr11:73578001
|
G | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-19+19922C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73578001 | ||||||
| chr11:73578180
|
G | A | 3 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0028 | 3 | HG02451.hp1 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-19+19743C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73578180 | ||||||
| chr11:73578260
|
G | A | 3 | a0001c0002t0001g0052a0001c0002t0020g0040a0001c0002t0023g0051 | 3 | HG01167.hp1 HG01169.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.-19+19663C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73578260 | ||||||
| chr11:73578631
|
G | A | 1 | a0001c0001t0017g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-19+19292C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73578631 | ||||||
| chr11:73578904
|
A | G | 1 | a0001c0002t0001g0129 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-19+19019T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73578904 | ||||||
| chr11:73579118
|
A | G | 56 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(53): Show | 56 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(53): Show |
intron_variant | MODIFIER | c.-19+18805T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73579118 | ||||||
| chr11:73579123
|
C | T | 2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+18800G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73579123 | ||||||
| chr11:73579310
|
T | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-19+18613A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73579310 | ||||||
| chr11:73579442
|
T | C | 22 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(19): Show | 22 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+18481A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73579442 | ||||||
| chr11:73579688
|
T | G | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+18235A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73579688 | ||||||
| chr11:73579847
|
G | A | 20 | a0001c0001t0004g0142a0001c0001t0004g0143a0001c0001t0004g0145others(17): Show | 20 | HG02109.hp2 HG02258.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.-19+18076C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73579847 | ||||||
| chr11:73579937
|
A | C | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+17986T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73579937 | ||||||
| chr11:73579941
|
T | A | 3 | a0001c0001t0011g0148a0001c0001t0011g0149a0001c0001t0011g0150 | 3 | HG02895.hp2 HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-19+17982A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73579941 | ||||||
| chr11:73580104
|
A | T | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-19+17819T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73580104 | ||||||
| chr11:73580117
|
A | G | 1 | a0001c0002t0001g0042 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-19+17806T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73580117 | ||||||
| chr11:73580210
|
C | T | 22 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(19): Show | 22 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+17713G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73580210 | ||||||
| chr11:73580808
|
C | T | 2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+17115G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73580808 | ||||||
| chr11:73581040
|
A | C | 26 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(23): Show | 26 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+16883T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73581040 | ||||||
| chr11:73581044
|
C | A | 10 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(7): Show | 10 | HG01255.hp1 HG01257.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19+16879G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73581044 | ||||||
| chr11:73581082
|
C | T | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-19+16841G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73581082 | ||||||
| chr11:73581156
|
A | G | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-19+16767T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73581156 | ||||||
| chr11:73581250
|
G | A | 4 | a0001c0002t0001g0075a0001c0002t0012g0113a0001c0002t0031g0111others(1): Show | 4 | HG02040.hp1 NA18984.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+16673C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73581250 | ||||||
| chr11:73581293
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-19+16630C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73581293 | ||||||
| chr11:73581586
|
C | T | 2 | a0001c0001t0007g0022a0001c0001t0007g0023 | 2 | HG01167.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-19+16337G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73581586 | ||||||
| chr11:73581609
|
A | G | 1 | a0001c0002t0021g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-19+16314T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73581609 | ||||||
| chr11:73581726
|
G | GT | 6 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+16196dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73581726 | ||||||
| chr11:73581726
|
GT | G | 5 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(2): Show | 5 | HG01106.hp2 HG01884.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+16196delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73581726 | ||||||
| chr11:73581779
|
C | T | 1 | a0001c0001t0037g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-19+16144G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73581779 | ||||||
| chr11:73581868
|
G | A | 1 | a0001c0002t0001g0065 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-19+16055C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73581868 | ||||||
| chr11:73581908
|
G | A | 10 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+16015C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73581908 | ||||||
| chr11:73581980
|
G | A | 2 | a0001c0002t0001g0053a0001c0002t0021g0054 | 2 | HG02083.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-19+15943C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73581980 | ||||||
| chr11:73582037
|
G | A | 93 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(90): Show | 93 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.-19+15886C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73582037 | ||||||
| chr11:73582067
|
C | T | 10 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(7): Show | 10 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+15856G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73582067 | ||||||
| chr11:73582435
|
T | A | 58 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(55): Show | 58 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(55): Show |
intron_variant | MODIFIER | c.-19+15488A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73582435 | ||||||
| chr11:73582512
|
T | C | 1 | a0002c0005t0001g0055 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-19+15411A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73582512 | ||||||
| chr11:73582726
|
T | G | 24 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(21): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+15197A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73582726 | ||||||
| chr11:73582788
|
A | G | 2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+15135T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73582788 | ||||||
| chr11:73582959
|
C | T | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+14964G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73582959 | ||||||
| chr11:73582978
|
G | C | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+14945C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73582978 | ||||||
| chr11:73583061
|
T | C | 24 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(21): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+14862A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73583061 | ||||||
| chr11:73583131
|
C | T | 1 | a0001c0002t0001g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-19+14792G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73583131 | ||||||
| chr11:73583260
|
G | A | 1 | a0001c0001t0037g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-19+14663C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73583260 | ||||||
| chr11:73583342
|
G | C | 2 | a0001c0001t0007g0026a0001c0001t0007g0027 | 2 | HG02683.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-19+14581C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73583342 | ||||||
| chr11:73583433
|
T | C | 56 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(53): Show | 56 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(53): Show |
intron_variant | MODIFIER | c.-19+14490A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73583433 | ||||||
| chr11:73583499
|
A | G | 8 | a0001c0002t0009g0073a0001c0002t0009g0076a0001c0002t0009g0105others(5): Show | 8 | HG01257.hp2 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+14424T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73583499 | ||||||
| chr11:73583788
|
C | T | 24 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(21): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+14135G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73583788 | ||||||
| chr11:73583815
|
G | A | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19+14108C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73583815 | ||||||
| chr11:73583821
|
G | C | 2 | a0001c0002t0046g0100a0001c0002t0047g0114 | 2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-19+14102C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73583821 | ||||||
| chr11:73584178
|
CT | C | 56 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(53): Show | 56 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(53): Show |
intron_variant | MODIFIER | c.-19+13744delA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73584178 | ||||||
| chr11:73584230
|
T | C | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-19+13693A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73584230 | ||||||
| chr11:73584469
|
C | CT | 13 | a0001c0001t0017g0032a0001c0001t0019g0069a0001c0001t0019g0070others(10): Show | 13 | HG01106.hp2 HG01255.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19+13453dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73584469 | ||||||
| chr11:73584469
|
CTTTTT | C | 21 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(18): Show | 21 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.-19+13449_-19+1345 others(9): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73584469 | ||||||
| chr11:73584567
|
G | A | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+13356C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73584567 | ||||||
| chr11:73584575
|
G | A | 24 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(21): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+13348C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73584575 | ||||||
| chr11:73584757
|
G | A | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+13166C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73584757 | ||||||
| chr11:73584783
|
C | T | 24 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(21): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+13140G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73584783 | ||||||
| chr11:73584876
|
T | C | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19+13047A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73584876 | ||||||
| chr11:73584883
|
CGAGCACT others(5): Show |
C | 24 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(21): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+13028_-19+1303 others(16): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73584883 | ||||||
| chr11:73585130
|
A | G | 3 | a0001c0001t0011g0148a0001c0001t0011g0149a0001c0001t0011g0150 | 3 | HG02895.hp2 HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-19+12793T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73585130 | ||||||
| chr11:73585265
|
A | G | 24 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(21): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+12658T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73585265 | ||||||
| chr11:73585511
|
C | T | 1 | a0001c0001t0006g0180 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-19+12412G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73585511 | ||||||
| chr11:73585595
|
T | G | 1 | a0001c0002t0001g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-19+12328A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73585595 | ||||||
| chr11:73585871
|
CA | C | 144 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0008others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-19+12051delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73585871 | ||||||
| chr11:73585871
|
CAA | C | 10 | a0001c0001t0002g0006a0001c0001t0018g0130a0001c0001t0041g0134others(7): Show | 10 | HG01167.hp1 HG02258.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19+12050_-19+1205 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73585871 | ||||||
| chr11:73585871
|
CAAAAAAA others(1): Show |
C | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+12044_-19+1205 others(12): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73585871 | ||||||
| chr11:73585883
|
A | C | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19+12040T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73585883 | ||||||
| chr11:73585913
|
T | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-19+12010A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73585913 | ||||||
| chr11:73585955
|
C | T | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+11968G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73585955 | ||||||
| chr11:73586007
|
G | A | 1 | a0001c0001t0037g0177 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-19+11916C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73586007 | ||||||
| chr11:73586018
|
C | T | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+11905G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73586018 | ||||||
| chr11:73586227
|
C | G | 4 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+11696G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73586227 | ||||||
| chr11:73586644
|
T | G | 3 | a0001c0001t0004g0145a0001c0001t0004g0147a0001c0001t0027g0146 | 3 | HG02717.hp2 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-19+11279A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73586644 | ||||||
| chr11:73587152
|
T | TA | 29 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(26): Show | 29 | HG00438.hp2 HG01433.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.-19+10770dupT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73587152 | ||||||
| chr11:73587152
|
T | TAA | 17 | a0001c0001t0004g0145a0001c0001t0004g0147a0001c0001t0004g0151others(14): Show | 17 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19+10769_-19+1077 others(6): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73587152 | ||||||
| chr11:73587152
|
T | TAAA | 14 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(11): Show | 14 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19+10768_-19+1077 others(7): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73587152 | ||||||
| chr11:73587152
|
TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0025g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-19+10760_-19+1077 others(15): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73587152 | ||||||
| chr11:73587167
|
A | AC | 8 | a0001c0001t0006g0024a0001c0001t0006g0067a0001c0001t0006g0180others(5): Show | 8 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+10755_-19+1075 others(5): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73587167 | ||||||
| chr11:73587174
|
A | C | 1 | a0001c0002t0001g0079 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-19+10749T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73587174 | ||||||
| chr11:73587453
|
C | T | 48 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(45): Show | 48 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(45): Show |
intron_variant | MODIFIER | c.-19+10470G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73587453 | ||||||
| chr11:73587472
|
A | G | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+10451T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73587472 | ||||||
| chr11:73587788
|
C | T | 1 | a0001c0002t0033g0077 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-19+10135G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73587788 | ||||||
| chr11:73587880
|
G | C | 1 | a0001c0001t0052g0157 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-19+10043C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73587880 | ||||||
| chr11:73588029
|
C | T | 8 | a0001c0001t0004g0145a0001c0001t0004g0147a0001c0001t0004g0151others(5): Show | 8 | HG02717.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+9894G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73588029 | ||||||
| chr11:73588477
|
G | C | 1 | a0001c0002t0001g0099 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-19+9446C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73588477 | ||||||
| chr11:73588682
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-19+9241C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73588682 | ||||||
| chr11:73588754
|
G | A | 11 | a0001c0001t0006g0020a0001c0001t0006g0021a0001c0001t0006g0024others(8): Show | 11 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+9169C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73588754 | ||||||
| chr11:73588966
|
A | G | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+8957T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73588966 | ||||||
| chr11:73589044
|
G | A | 1 | a0001c0002t0032g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-19+8879C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73589044 | ||||||
| chr11:73589114
|
T | C | 1 | a0001c0002t0001g0117 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-19+8809A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73589114 | ||||||
| chr11:73589177
|
C | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+8746G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73589177 | ||||||
| chr11:73589265
|
A | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+8658T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73589265 | ||||||
| chr11:73589388
|
G | T | 3 | a0001c0001t0004g0145a0001c0001t0004g0147a0001c0001t0027g0146 | 3 | HG02717.hp2 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-19+8535C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73589388 | ||||||
| chr11:73589406
|
A | C | 2 | a0001c0001t0007g0022a0001c0001t0007g0023 | 2 | HG01167.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-19+8517T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73589406 | ||||||
| chr11:73589480
|
G | A | 5 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(2): Show | 5 | HG00323.hp1 HG02258.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+8443C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73589480 | ||||||
| chr11:73589495
|
GA | G | 6 | a0001c0001t0002g0005a0001c0001t0016g0135a0001c0001t0016g0136others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+8427delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73589495 | ||||||
| chr11:73589564
|
G | A | 20 | a0001c0001t0004g0142a0001c0001t0004g0143a0001c0001t0004g0145others(17): Show | 20 | HG02109.hp2 HG02258.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.-19+8359C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73589564 | ||||||
| chr11:73589597
|
G | A | 34 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(31): Show | 34 | HG00544.hp1 HG01069.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.-19+8326C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73589597 | ||||||
| chr11:73589835
|
G | A | 1 | a0001c0001t0018g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19+8088C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73589835 | ||||||
| chr11:73589859
|
G | A | 1 | a0001c0001t0016g0136 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-19+8064C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73589859 | ||||||
| chr11:73589896
|
C | T | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-19+8027G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73589896 | ||||||
| chr11:73589966
|
T | C | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+7957A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73589966 | ||||||
| chr11:73589996
|
G | A | 2 | a0001c0002t0001g0058a0001c0002t0005g0059 | 2 | NA18981.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-19+7927C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73589996 | ||||||
| chr11:73590139
|
T | C | 30 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(27): Show | 30 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19+7784A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73590139 | ||||||
| chr11:73590180
|
T | C | 26 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(23): Show | 26 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+7743A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73590180 | ||||||
| chr11:73590198
|
T | G | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+7725A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73590198 | ||||||
| chr11:73590355
|
A | G | 1 | a0001c0001t0022g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-19+7568T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73590355 | ||||||
| chr11:73590441
|
A | G | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+7482T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73590441 | ||||||
| chr11:73590448
|
T | C | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19+7475A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73590448 | ||||||
| chr11:73590525
|
C | G | 2 | a0001c0001t0006g0020a0001c0001t0006g0021 | 2 | HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-19+7398G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73590525 | ||||||
| chr11:73590803
|
G | A | 2 | a0001c0001t0014g0153a0001c0001t0014g0154 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-19+7120C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73590803 | ||||||
| chr11:73590813
|
A | G | 8 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(5): Show | 8 | HG01884.hp1 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+7110T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73590813 | ||||||
| chr11:73590841
|
A | G | 24 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(21): Show | 24 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+7082T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73590841 | ||||||
| chr11:73591659
|
G | A | 1 | a0001c0001t0002g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-19+6264C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73591659 | ||||||
| chr11:73591691
|
G | C | 2 | a0001c0002t0001g0118a0001c0002t0001g0119 | 2 | NA18983.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-19+6232C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73591691 | ||||||
| chr11:73591723
|
T | C | 56 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(53): Show | 56 | HG00140.hp2 HG01167.hp2 HG01255.hp2 others(53): Show |
intron_variant | MODIFIER | c.-19+6200A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73591723 | ||||||
| chr11:73591756
|
C | T | 1 | a0001c0002t0046g0100 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-19+6167G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73591756 | ||||||
| chr11:73591891
|
C | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+6032G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73591891 | ||||||
| chr11:73592068
|
C | G | 130 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(127): Show | 130 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.-19+5855G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73592068 | ||||||
| chr11:73592281
|
G | T | 2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+5642C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73592281 | ||||||
| chr11:73592664
|
G | T | 1 | a0001c0002t0009g0076 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-19+5259C>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73592664 | ||||||
| chr11:73592722
|
C | T | 18 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(15): Show | 18 | HG02109.hp2 HG02451.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.-19+5201G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73592722 | ||||||
| chr11:73592872
|
CA | C | 107 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(104): Show | 107 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-19+5050delT | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73592872 | ||||||
| chr11:73592966
|
C | T | 26 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(23): Show | 26 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+4957G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73592966 | ||||||
| chr11:73593101
|
A | AGGGATAT others(6): Show |
1 | a0001c0002t0001g0075 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-19+4809_-19+4821d others(15): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73593101 | ||||||
| chr11:73593370
|
T | C | 1 | a0001c0002t0001g0124 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-19+4553A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73593370 | ||||||
| chr11:73593556
|
A | G | 3 | a0001c0002t0009g0073a0001c0002t0049g0072a0001c0004t0009g0074 | 3 | HG02630.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-19+4367T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73593556 | ||||||
| chr11:73593596
|
T | C | 10 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(7): Show | 10 | HG01106.hp2 HG01884.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+4327A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73593596 | ||||||
| chr11:73593753
|
T | C | 4 | a0001c0001t0014g0153a0001c0001t0014g0154a0001c0001t0015g0132others(1): Show | 4 | HG02258.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+4170A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73593753 | ||||||
| chr11:73593806
|
C | T | 1 | a0001c0001t0022g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-19+4117G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73593806 | ||||||
| chr11:73593820
|
G | A | 22 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(19): Show | 22 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+4103C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73593820 | ||||||
| chr11:73593902
|
T | A | 2 | a0001c0001t0039g0125a0001c0001t0040g0126 | 2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-19+4021A>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73593902 | ||||||
| chr11:73594266
|
A | AT | 8 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(5): Show | 8 | HG02145.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+3656dupA | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73594266 | ||||||
| chr11:73594280
|
T | G | 1 | a0001c0002t0001g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-19+3643A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73594280 | ||||||
| chr11:73594525
|
GGTTTTTT others(4): Show |
G | 4 | a0001c0001t0019g0069a0001c0001t0019g0070a0001c0001t0042g0060others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+3387_-19+3397d others(13): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73594525 | ||||||
| chr11:73594814
|
C | A | 116 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(113): Show | 116 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.-19+3109G>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73594814 | ||||||
| chr11:73594916
|
C | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | HG02451.hp2 HG02630.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+3007G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73594916 | ||||||
| chr11:73594978
|
A | T | 6 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(3): Show | 6 | HG02622.hp2 HG02818.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+2945T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73594978 | ||||||
| chr11:73594989
|
G | C | 26 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(23): Show | 26 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+2934C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73594989 | ||||||
| chr11:73595140
|
T | G | 3 | a0001c0001t0018g0128a0001c0001t0018g0130a0001c0002t0001g0129 | 3 | HG02572.hp1 HG02895.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-19+2783A>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73595140 | ||||||
| chr11:73595147
|
C | G | 1 | a0001c0001t0017g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-19+2776G>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73595147 | ||||||
| chr11:73595316
|
G | C | 1 | a0001c0002t0050g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-19+2607C>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73595316 | ||||||
| chr11:73595444
|
A | C | 2 | a0001c0001t0015g0132a0001c0001t0015g0133 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+2479T>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73595444 | ||||||
| chr11:73595691
|
T | C | 1 | a0001c0002t0050g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-19+2232A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73595691 | ||||||
| chr11:73595711
|
G | A | 26 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139others(23): Show | 26 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.-19+2212C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73595711 | ||||||
| chr11:73595730
|
C | T | 2 | a0001c0002t0001g0065a0001c0002t0001g0066 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-19+2193G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73595730 | ||||||
| chr11:73595821
|
C | T | 2 | a0001c0003t0004g0063a0001c0003t0028g0064 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19+2102G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73595821 | ||||||
| chr11:73596296
|
G | A | 4 | a0001c0001t0010g0001a0001c0001t0010g0002a0001c0001t0010g0004others(1): Show | 4 | NA18965.hp1 NA18981.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+1627C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73596296 | ||||||
| chr11:73596376
|
T | C | 1 | a0001c0002t0005g0155 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-19+1547A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73596376 | ||||||
| chr11:73596386
|
T | C | 1 | a0001c0001t0030g0156 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-19+1537A>G | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73596386 | ||||||
| chr11:73596509
|
A | G | 2 | a0001c0001t0022g0061a0001c0001t0022g0062 | 2 | HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-19+1414T>C | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73596509 | ||||||
| chr11:73596699
|
C | T | 1 | a0001c0001t0042g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-19+1224G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73596699 | ||||||
| chr11:73596717
|
A | T | 27 | a0001c0002t0001g0033a0001c0002t0001g0034a0001c0002t0001g0035others(24): Show | 27 | HG00438.hp2 HG01109.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.-19+1206T>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73596717 | ||||||
| chr11:73597267
|
C | T | 1 | a0001c0001t0052g0157 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-19+656G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73597267 | ||||||
| chr11:73597383
|
C | T | 1 | a0001c0001t0017g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-19+540G>A | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73597383 | ||||||
| chr11:73597496
|
G | A | 168 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(165): Show | 168 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.-19+427C>T | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73597496 | ||||||
| chr11:73597724
|
AC | A | 24 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(21): Show | 24 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+198delG | FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | 73597724 |