| geneid | 8603 |
|---|---|
| ensemblid | ENSG00000125386.16 |
| hgncid | 16822 |
| symbol | FAM193A |
| name | family with sequence similarity 193 member A |
| refseq_nuc | NM_001366318.2 |
| refseq_prot | NP_001353247.1 |
| ensembl_nuc | ENST00000637812.2 |
| ensembl_prot | ENSP00000490564.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 2536647 |
| end | 2732573 |
| strand | + |
| ver | v1.2 |
| region | chr4:2536647-2732573 |
| region5000 | chr4:2531647-2737573 |
| regionname0 | FAM193A_chr4_2536647_2732573 |
| regionname5000 | FAM193A_chr4_2531647_2737573 |
| 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 | 1515 | 258 | 46 | 53 | 113 | 12 | 32 | 80 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0002 | 0/0 | 26 | 12 | 2 | 3 | 4 | 1 | 2 | 3 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0003 | 0/0 | 1515 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0004 | 0/0 | 1515 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0005 | 0/0 | 1515 | 9 | 2 | 2 | 2 | 0 | 3 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0006 | 0/0 | 1515 | 8 | 5 | 0 | 2 | 0 | 1 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0007 | 0/0 | 1515 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0008 | 0/0 | 1515 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0009 | 0/0 | 1515 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0010 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0011 | 0/0 | 1515 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0012 | 0/0 | 1515 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0013 | 0/0 | 1515 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0014 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0015 | 0/0 | 1515 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 4548 | 242 | 35 | 51 | 113 | 11 | 30 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0002 | 0/0 | 4548 | 12 | 8 | 1 | 0 | 1 | 2 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0003 | 0/0 | 4548 | 12 | 12 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0004 | 0/0 | 4548 | 10 | 10 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0005 | 0/0 | 4548 | 9 | 2 | 2 | 2 | 0 | 3 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0006 | 0/0 | 4549 | 8 | 1 | 3 | 2 | 0 | 2 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0007 | 0/0 | 4548 | 8 | 8 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0008 | 0/0 | 4548 | 8 | 5 | 0 | 2 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0009 | 0/0 | 4548 | 4 | 0 | 0 | 4 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0010 | 0/0 | 4548 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0011 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0012 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0013 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0014 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0015 | 0/0 | 4548 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0016 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0017 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0018 | 0/0 | 4548 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0019 | 0/0 | 4548 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0020 | 0/0 | 4548 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0021 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0022 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0023 | 0/0 | 4548 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0024 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| c0025 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| 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 | 975 | 179 | 54 | 26 | 70 | 8 | 19 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| t0002 | 0/0 | 975 | 96 | 5 | 28 | 43 | 5 | 15 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| t0003 | 0/0 | 975 | 16 | 14 | 0 | 0 | 1 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| t0004 | 0/0 | 975 | 15 | 2 | 2 | 9 | 0 | 2 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| t0005 | 0/0 | 975 | 5 | 5 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| t0006 | 0/0 | 975 | 4 | 0 | 1 | 3 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| t0007 | 0/0 | 975 | 3 | 2 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| t0008 | 0/0 | 974 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| t0009 | 0/0 | 974 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| t0010 | 0/0 | 975 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| t0011 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| t0012 | 0/0 | 975 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| t0013 | 0/0 | 975 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| t0014 | 0/0 | 974 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| t0015 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| t0016 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| t0017 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| t0018 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0251 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4548 | 242 | 35 | 51 | 113 | 11 | 30 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0002 | 0/0 | 4548 | 12 | 8 | 1 | 0 | 1 | 2 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0016 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0018 | 0/0 | 4548 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0021 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0025 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0002c0006 | 0/0 | 4549 | 8 | 1 | 3 | 2 | 0 | 2 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0002c0011 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0002c0012 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0002c0013 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0002c0014 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0003c0003 | 0/0 | 4548 | 12 | 12 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0004c0004 | 0/0 | 4548 | 10 | 10 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0004c0017 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0005c0005 | 0/0 | 4548 | 9 | 2 | 2 | 2 | 0 | 3 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0006c0008 | 0/0 | 4548 | 8 | 5 | 0 | 2 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0007c0007 | 0/0 | 4548 | 8 | 8 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0008c0009 | 0/0 | 4548 | 4 | 0 | 0 | 4 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0009c0010 | 0/0 | 4548 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0010c0022 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0011c0023 | 0/0 | 4548 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0012c0020 | 0/0 | 4548 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0013c0019 | 0/0 | 4548 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0014c0024 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0015c0015 | 0/0 | 4548 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5522 | 138 | 26 | 22 | 62 | 8 | 18 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0001t0002 | 0/0 | 5522 | 88 | 5 | 25 | 43 | 3 | 12 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0001t0003 | 0/0 | 5522 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0001t0004 | 0/0 | 5522 | 5 | 0 | 0 | 5 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0001t0006 | 0/0 | 5522 | 4 | 0 | 1 | 3 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0001t0007 | 0/0 | 5522 | 2 | 1 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0001t0008 | 0/0 | 5521 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0001t0010 | 0/0 | 5522 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0001t0012 | 0/0 | 5522 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0002t0001 | 0/0 | 5522 | 5 | 4 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0002t0003 | 0/0 | 5522 | 4 | 2 | 0 | 0 | 1 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0002t0009 | 0/0 | 5521 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0002t0013 | 0/0 | 5522 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0002t0016 | 0/0 | 5522 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0016t0001 | 0/0 | 5522 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0018t0001 | 0/0 | 5522 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0021t0003 | 0/0 | 5522 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0001c0025t0001 | 0/0 | 5522 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0002c0006t0001 | 0/0 | 5523 | 3 | 1 | 1 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0002c0006t0002 | 0/0 | 5523 | 4 | 0 | 2 | 0 | 0 | 2 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0002c0006t0017 | 0/0 | 5523 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0002c0011t0003 | 0/0 | 5523 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0002c0012t0004 | 0/0 | 5523 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0002c0013t0002 | 0/0 | 5523 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0002c0014t0001 | 0/0 | 5523 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0003c0003t0001 | 0/0 | 5522 | 5 | 5 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0003c0003t0004 | 0/0 | 5522 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0003c0003t0005 | 0/0 | 5522 | 5 | 5 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0003c0003t0011 | 0/0 | 5522 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0004c0004t0001 | 0/0 | 5522 | 7 | 7 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0004c0004t0003 | 0/0 | 5522 | 3 | 3 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0004c0017t0001 | 0/0 | 5522 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0005c0005t0002 | 0/0 | 5522 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0005c0005t0004 | 0/0 | 5522 | 7 | 1 | 2 | 2 | 0 | 2 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0005c0005t0007 | 0/0 | 5522 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0006c0008t0001 | 0/0 | 5522 | 8 | 5 | 0 | 2 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0007c0007t0001 | 0/0 | 5522 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0007c0007t0003 | 0/0 | 5522 | 6 | 6 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0008c0009t0001 | 0/0 | 5522 | 4 | 0 | 0 | 4 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0009c0010t0014 | 0/0 | 5521 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0009c0010t0015 | 0/0 | 5522 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0010c0022t0001 | 0/0 | 5522 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0011c0023t0001 | 0/0 | 5522 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0012c0020t0004 | 0/0 | 5522 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0013c0019t0002 | 0/0 | 5522 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0014c0024t0018 | 0/0 | 5522 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| a0015c0015t0002 | 0/0 | 5522 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | copy fasta | chr4 | 2531647 | 2737573 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0251 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0007g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0007g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0010g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0001t0012g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0002t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0002t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0002t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0002t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0002t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0002t0013g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0002t0016g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0016t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0018t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0021t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0001c0025t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0002c0006t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0002c0006t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0002c0006t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0002c0006t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0002c0006t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0002c0006t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0002c0006t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0002c0006t0017g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0002c0011t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0002c0012t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0002c0013t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0002c0014t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0003c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0003c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0003c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0003c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0003c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0003c0003t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0003c0003t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0003c0003t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0003c0003t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0003c0003t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0003c0003t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0003c0003t0011g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0004c0004t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0004c0004t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0004c0004t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0004c0004t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0004c0004t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0004c0004t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0004c0004t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0004c0004t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0004c0004t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0004c0004t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0004c0017t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0005c0005t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0005c0005t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0005c0005t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0005c0005t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0005c0005t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0005c0005t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0005c0005t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0005c0005t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0005c0005t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0006c0008t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0006c0008t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0006c0008t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0006c0008t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0006c0008t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0006c0008t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0006c0008t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0006c0008t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0007c0007t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0007c0007t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0007c0007t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0007c0007t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0007c0007t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0007c0007t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0007c0007t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0007c0007t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0008c0009t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0008c0009t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0008c0009t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0008c0009t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0009c0010t0014g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0009c0010t0015g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0010c0022t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0011c0023t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0012c0020t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0013c0019t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0014c0024t0018g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| a0015c0015t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0026 | EUR | GBR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0306 | EUR | GBR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | GBR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | GBR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | FIN | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00280 | hp2 | a0015 | c0015 | t0002 | g0028 | EUR | FIN | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0271 | EUR | FIN | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0043 | EUR | FIN | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00408 | hp1 | a0005 | c0005 | t0004 | g0134 | EAS | CHS | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0196 | EAS | CHS | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00544 | hp2 | a0002 | c0006 | t0001 | g0268 | EAS | CHS | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | CHS | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00609 | hp2 | a0006 | c0008 | t0001 | g0124 | EAS | CHS | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00735 | hp2 | a0001 | c0018 | t0001 | g0260 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG00741 | hp2 | a0002 | c0006 | t0001 | g0287 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01074 | hp1 | a0005 | c0005 | t0004 | g0135 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01099 | hp1 | a0002 | c0006 | t0002 | g0060 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01109 | hp1 | a0011 | c0023 | t0001 | g0247 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0129 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01192 | hp2 | a0002 | c0006 | t0002 | g0102 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01243 | hp1 | a0001 | c0001 | t0012 | g0148 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0037 | AMR | CLM | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | CLM | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01361 | hp2 | a0001 | c0001 | t0010 | g0149 | AMR | CLM | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01516 | hp1 | a0001 | c0002 | t0003 | g0112 | EUR | IBS | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | IBS | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0263 | EUR | IBS | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01517 | hp2 | a0002 | c0013 | t0002 | g0018 | EUR | IBS | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01884 | hp1 | a0014 | c0024 | t0018 | g0139 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01891 | hp1 | a0007 | c0007 | t0003 | g0107 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0234 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PEL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01975 | hp1 | a0013 | c0019 | t0002 | g0055 | AMR | PEL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01975 | hp2 | a0005 | c0005 | t0004 | g0136 | AMR | PEL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02055 | hp1 | a0002 | c0006 | t0001 | g0242 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0240 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02145 | hp1 | a0004 | c0004 | t0001 | g0323 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CDX | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | CDX | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02257 | hp1 | a0004 | c0004 | t0001 | g0326 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02257 | hp2 | a0003 | c0003 | t0005 | g0190 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02258 | hp2 | a0004 | c0004 | t0001 | g0318 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02572 | hp1 | a0003 | c0003 | t0004 | g0155 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02572 | hp2 | a0001 | c0021 | t0003 | g0143 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02615 | hp1 | a0004 | c0004 | t0001 | g0322 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02615 | hp2 | a0002 | c0011 | t0003 | g0114 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02622 | hp2 | a0004 | c0004 | t0003 | g0320 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02630 | hp2 | a0004 | c0004 | t0001 | g0321 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02717 | hp1 | a0007 | c0007 | t0003 | g0108 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02717 | hp2 | a0005 | c0005 | t0004 | g0130 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02723 | hp1 | a0004 | c0004 | t0003 | g0319 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02723 | hp2 | a0007 | c0007 | t0003 | g0111 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02818 | hp1 | a0006 | c0008 | t0001 | g0127 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02818 | hp2 | a0001 | c0002 | t0009 | g0239 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0235 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0329 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02895 | hp1 | a0006 | c0008 | t0001 | g0216 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02896 | hp1 | a0003 | c0003 | t0001 | g0238 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02922 | hp1 | a0007 | c0007 | t0003 | g0109 | AFR | ESN | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02922 | hp2 | a0001 | c0016 | t0001 | g0308 | AFR | ESN | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0119 | AFR | ESN | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02970 | hp2 | a0003 | c0003 | t0005 | g0164 | AFR | ESN | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02976 | hp1 | a0003 | c0003 | t0005 | g0187 | AFR | ESN | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03017 | hp1 | a0002 | c0006 | t0002 | g0105 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0116 | AFR | GWD | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03098 | hp2 | a0003 | c0003 | t0001 | g0233 | AFR | MSL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03130 | hp2 | a0009 | c0010 | t0015 | g0229 | AFR | ESN | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0215 | AFR | ESN | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03195 | hp1 | a0007 | c0007 | t0003 | g0106 | AFR | ESN | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0137 | AFR | MSL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03209 | hp2 | a0003 | c0003 | t0005 | g0188 | AFR | MSL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03225 | hp2 | a0004 | c0004 | t0003 | g0317 | AFR | MSL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03453 | hp1 | a0007 | c0007 | t0001 | g0115 | AFR | MSL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03453 | hp2 | a0001 | c0002 | t0016 | g0023 | AFR | MSL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | MSL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03486 | hp2 | a0003 | c0003 | t0005 | g0189 | AFR | MSL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03579 | hp1 | a0010 | c0022 | t0001 | g0227 | AFR | MSL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03579 | hp2 | a0007 | c0007 | t0001 | g0110 | AFR | MSL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03654 | hp1 | a0005 | c0005 | t0004 | g0128 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03669 | hp1 | a0005 | c0005 | t0004 | g0140 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03704 | hp2 | a0001 | c0002 | t0013 | g0117 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0120 | SAS | BEB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03834 | hp2 | a0006 | c0008 | t0001 | g0121 | SAS | BEB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03927 | hp1 | a0005 | c0005 | t0002 | g0138 | SAS | BEB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03927 | hp2 | a0002 | c0006 | t0002 | g0046 | SAS | BEB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | BEB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | BEB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | BEB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0330 | SAS | STU | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | STU | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0236 | AFR | YRI | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | YRI | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | CHB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | CHB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18747 | hp1 | a0001 | c0001 | t0006 | g0052 | EAS | CHB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18906 | hp1 | a0004 | c0017 | t0001 | g0324 | AFR | YRI | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18906 | hp2 | a0007 | c0007 | t0003 | g0118 | AFR | YRI | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0042 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18944 | hp2 | a0008 | c0009 | t0001 | g0266 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18947 | hp2 | a0008 | c0009 | t0001 | g0295 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18957 | hp2 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18960 | hp1 | a0012 | c0020 | t0004 | g0192 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0316 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18981 | hp1 | a0002 | c0006 | t0017 | g0096 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18981 | hp2 | a0002 | c0014 | t0001 | g0270 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18984 | hp1 | a0005 | c0005 | t0004 | g0141 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18984 | hp2 | a0008 | c0009 | t0001 | g0310 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19007 | hp1 | a0006 | c0008 | t0001 | g0005 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19030 | hp1 | a0006 | c0008 | t0001 | g0132 | AFR | LWK | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | LWK | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | LWK | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0113 | AFR | LWK | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19062 | hp2 | a0002 | c0012 | t0004 | g0328 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19070 | hp2 | a0008 | c0009 | t0001 | g0301 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ASW | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0249 | AFR | ASW | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0313 | EUR | TSI | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | TSI | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02109 | hp1 | a0005 | c0005 | t0007 | g0131 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02486 | hp2 | a0009 | c0010 | t0014 | g0228 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02559 | hp1 | a0001 | c0025 | t0001 | g0224 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG02559 | hp2 | a0006 | c0008 | t0001 | g0125 | AFR | ACB | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03471 | hp1 | a0004 | c0004 | t0001 | g0325 | AFR | MSL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | USA | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| HG06807 | hp2 | a0004 | c0004 | t0001 | g0327 | AFR | USA | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA20300 | hp1 | a0006 | c0008 | t0001 | g0126 | AFR | USA | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | USA | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA21309 | hp1 | a0003 | c0003 | t0011 | g0186 | AFR | LWK | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | LWK | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0251 | REF | REF | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0237 | REF | REF | FAM193A_chr4_2531647_2737573 | FAM193A | chr4 | 2531647 | 2737573 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:2536987
|
C | CG | 1 | a0002 | 12 | HG00544.hp2 HG00741.hp2 HG01099.hp1 others(9): Show |
frameshift_variant | HIGH | c.77dupG | p.Asn27fs | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/21 | 347/5522 | 78/4548 | 26/1515 | INFO_REALIGN_3_PRIME | chr4 | 2536987 | |
| chr4:2537066
|
G | A | 1 | a0015 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.151G>A | p.Ala51Thr | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/21 | 420/5522 | 151/4548 | 51/1515 | chr4 | 2537066 | ||
| chr4:2631039
|
C | T | 2 | a0002a0008 | 5 | NA18944.hp2 NA18947.hp2 NA18981.hp2 others(2): Show |
missense_variant | MODERATE | c.908C>T | p.Ala303Val | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/21 | 1177/5522 | 908/4548 | 303/1515 | chr4 | 2631039 | ||
| chr4:2657816
|
C | A | 1 | a0009 | 2 | HG02486.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.1325C>A | p.Thr442Asn | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/21 | 1594/5522 | 1325/4548 | 442/1515 | chr4 | 2657816 | ||
| chr4:2659615
|
A | G | 3 | a0003a0004a0014 | 24 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(21): Show |
missense_variant | MODERATE | c.1447A>G | p.Met483Val | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 9/21 | 1716/5522 | 1447/4548 | 483/1515 | chr4 | 2659615 | ||
| chr4:2660003
|
T | A | 1 | a0013 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.1694T>A | p.Ile565Asn | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/21 | 1963/5522 | 1694/4548 | 565/1515 | chr4 | 2660003 | ||
| chr4:2662965
|
G | A | 1 | a0012 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.1873G>A | p.Gly625Arg | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 11/21 | 2142/5522 | 1873/4548 | 625/1515 | chr4 | 2662965 | ||
| chr4:2663247
|
A | G | 1 | a0006 | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
missense_variant | MODERATE | c.2038A>G | p.Ser680Gly | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/21 | 2307/5522 | 2038/4548 | 680/1515 | chr4 | 2663247 | ||
| chr4:2672185
|
C | A | 1 | a0009 | 2 | HG02486.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.2144C>A | p.Pro715Gln | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/21 | 2413/5522 | 2144/4548 | 715/1515 | chr4 | 2672185 | ||
| chr4:2672356
|
C | G | 1 | a0011 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.2315C>G | p.Pro772Arg | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/21 | 2584/5522 | 2315/4548 | 772/1515 | chr4 | 2672356 | ||
| chr4:2690782
|
C | T | 1 | a0010 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.2615C>T | p.Ser872Leu | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/21 | 2884/5522 | 2615/4548 | 872/1515 | chr4 | 2690782 | ||
| chr4:2693799
|
C | T | 1 | a0002 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.3017C>T | p.Thr1006Ile | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 16/21 | 3286/5522 | 3017/4548 | 1006/1515 | chr4 | 2693799 | ||
| chr4:2699945
|
A | G | 1 | a0007 | 8 | HG01891.hp1 HG02717.hp1 HG02723.hp2 others(5): Show |
missense_variant | MODERATE | c.3773A>G | p.Asn1258Ser | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/21 | 4042/5522 | 3773/4548 | 1258/1515 | chr4 | 2699945 | ||
| chr4:2700089
|
A | G | 1 | a0007 | 8 | HG01891.hp1 HG02717.hp1 HG02723.hp2 others(5): Show |
missense_variant | MODERATE | c.3917A>G | p.Lys1306Arg | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/21 | 4186/5522 | 3917/4548 | 1306/1515 | chr4 | 2700089 | ||
| chr4:2700339
|
G | C | 2 | a0003a0014 | 13 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
missense_variant | MODERATE | c.4167G>C | p.Glu1389Asp | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/21 | 4436/5522 | 4167/4548 | 1389/1515 | chr4 | 2700339 | ||
| chr4:2700388
|
A | G | 3 | a0002a0005a0014 | 11 | HG00408.hp1 HG01074.hp1 HG01884.hp1 others(8): Show |
missense_variant | MODERATE | c.4216A>G | p.Ile1406Val | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/21 | 4485/5522 | 4216/4548 | 1406/1515 | chr4 | 2700388 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:2596260
|
G | A | 4 | a0001c0016a0004c0004a0004c0017others(1): Show | 14 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(11): Show |
synonymous_variant | LOW | c.432G>A | p.Leu144Leu | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/21 | 701/5522 | 432/4548 | 144/1515 | chr4 | 2596260 | ||
| chr4:2626419
|
G | A | 1 | a0001c0018 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.645G>A | p.Ser215Ser | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/21 | 914/5522 | 645/4548 | 215/1515 | chr4 | 2626419 | ||
| chr4:2646748
|
C | T | 1 | a0001c0025 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.1227C>T | p.Tyr409Tyr | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/21 | 1496/5522 | 1227/4548 | 409/1515 | chr4 | 2646748 | ||
| chr4:2659980
|
C | T | 1 | a0009c0010 | 2 | HG02486.hp2 HG03130.hp2 |
synonymous_variant | LOW | c.1671C>T | p.Ser557Ser | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/21 | 1940/5522 | 1671/4548 | 557/1515 | chr4 | 2659980 | ||
| chr4:2672165
|
G | A | 3 | a0001c0021a0004c0004a0009c0010 | 13 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
synonymous_variant | LOW | c.2124G>A | p.Gln708Gln | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/21 | 2393/5522 | 2124/4548 | 708/1515 | chr4 | 2672165 | ||
| chr4:2693710
|
G | A | 1 | a0014c0024 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.2928G>A | p.Ala976Ala | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 16/21 | 3197/5522 | 2928/4548 | 976/1515 | chr4 | 2693710 | ||
| chr4:2693833
|
G | A | 1 | a0012c0020 | 1 | NA18960.hp1 | synonymous_variant | LOW | c.3051G>A | p.Pro1017Pro | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 16/21 | 3320/5522 | 3051/4548 | 1017/1515 | chr4 | 2693833 | ||
| chr4:2696503
|
G | A | 3 | a0001c0002a0002c0011a0007c0007 | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
synonymous_variant | LOW | c.3417G>A | p.Val1139Val | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/21 | 3686/5522 | 3417/4548 | 1139/1515 | chr4 | 2696503 | ||
| chr4:2700466
|
C | T | 1 | a0009c0010 | 2 | HG02486.hp2 HG03130.hp2 |
synonymous_variant | LOW | c.4294C>T | p.Leu1432Leu | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/21 | 4563/5522 | 4294/4548 | 1432/1515 | chr4 | 2700466 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:2536758
|
C | T | 1 | a0014c0024t0018 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-158C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/21 | 158 | chr4 | 2536758 | |||||
| chr4:2536874
|
C | T | 9 | a0001c0001t0002a0001c0001t0006a0001c0002t0016others(6): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-42C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/21 | chr4 | 2536874 | ||||||
| chr4:2732032
|
C | T | 2 | a0009c0010t0014a0009c0010t0015 | 2 | HG02486.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*164C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 164 | chr4 | 2732032 | |||||
| chr4:2732081
|
C | T | 1 | a0001c0002t0013 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*213C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 213 | chr4 | 2732081 | |||||
| chr4:2732189
|
C | T | 1 | a0001c0001t0012 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*321C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 321 | chr4 | 2732189 | |||||
| chr4:2732221
|
G | C | 8 | a0001c0001t0004a0001c0001t0006a0002c0012t0004others(5): Show | 21 | HG00408.hp1 HG00544.hp1 HG01074.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*353G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 353 | chr4 | 2732221 | |||||
| chr4:2732257
|
C | T | 2 | a0001c0001t0007a0005c0005t0007 | 3 | HG01167.hp2 HG02109.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*389C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 389 | chr4 | 2732257 | |||||
| chr4:2732292
|
C | T | 2 | a0002c0006t0017a0003c0003t0011 | 2 | NA18981.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*424C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 424 | chr4 | 2732292 | |||||
| chr4:2732396
|
CT | C | 3 | a0001c0001t0008a0001c0002t0009a0009c0010t0014 | 4 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*530delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 530 | INFO_REALIGN_3_PRIME | chr4 | 2732396 | ||||
| chr4:2732406
|
G | A | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*538G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 538 | chr4 | 2732406 | |||||
| chr4:2732409
|
A | C | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*541A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 541 | chr4 | 2732409 | |||||
| chr4:2732410
|
A | T | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*542A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 542 | chr4 | 2732410 | |||||
| chr4:2732411
|
A | G | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*543A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 543 | chr4 | 2732411 | |||||
| chr4:2732413
|
T | C | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*545T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 545 | chr4 | 2732413 | |||||
| chr4:2732418
|
A | G | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*550A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 550 | chr4 | 2732418 | |||||
| chr4:2732419
|
A | T | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*551A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 551 | chr4 | 2732419 | |||||
| chr4:2732422
|
A | G | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*554A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 554 | chr4 | 2732422 | |||||
| chr4:2732424
|
C | G | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*556C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 556 | chr4 | 2732424 | |||||
| chr4:2732425
|
C | G | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*557C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 557 | chr4 | 2732425 | |||||
| chr4:2732426
|
C | G | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*558C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 558 | chr4 | 2732426 | |||||
| chr4:2732428
|
C | T | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*560C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 560 | chr4 | 2732428 | |||||
| chr4:2732430
|
C | A | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*562C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 562 | chr4 | 2732430 | |||||
| chr4:2732432
|
G | A | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*564G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 564 | chr4 | 2732432 | |||||
| chr4:2732433
|
T | C | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*565T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 565 | chr4 | 2732433 | |||||
| chr4:2732436
|
T | A | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*568T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 568 | chr4 | 2732436 | |||||
| chr4:2732437
|
C | A | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*569C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 569 | chr4 | 2732437 | |||||
| chr4:2732441
|
C | G | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*573C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 573 | chr4 | 2732441 | |||||
| chr4:2732443
|
A | G | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*575A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 575 | chr4 | 2732443 | |||||
| chr4:2732444
|
T | C | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*576T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 576 | chr4 | 2732444 | |||||
| chr4:2732445
|
C | A | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*577C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 577 | chr4 | 2732445 | |||||
| chr4:2732447
|
A | C | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*579A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 579 | chr4 | 2732447 | |||||
| chr4:2732448
|
G | A | 9 | a0001c0001t0003a0001c0002t0003a0001c0002t0009others(6): Show | 19 | HG01516.hp1 HG01891.hp1 HG02572.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*580G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 580 | chr4 | 2732448 | |||||
| chr4:2732450
|
C | G | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*582C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 582 | chr4 | 2732450 | |||||
| chr4:2732452
|
G | A | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*584G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 584 | chr4 | 2732452 | |||||
| chr4:2732453
|
T | C | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*585T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 585 | chr4 | 2732453 | |||||
| chr4:2732454
|
T | A | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*586T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 586 | chr4 | 2732454 | |||||
| chr4:2732455
|
A | C | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*587A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 587 | chr4 | 2732455 | |||||
| chr4:2732457
|
A | G | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*589A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 589 | chr4 | 2732457 | |||||
| chr4:2732460
|
G | C | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*592G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 592 | chr4 | 2732460 | |||||
| chr4:2732461
|
T | A | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*593T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 593 | chr4 | 2732461 | |||||
| chr4:2732461
|
T | C | 1 | a0003c0003t0005 | 5 | HG02257.hp2 HG02970.hp2 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*593T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 593 | chr4 | 2732461 | |||||
| chr4:2732468
|
C | T | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*600C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 600 | chr4 | 2732468 | |||||
| chr4:2732472
|
A | G | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*604A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 604 | chr4 | 2732472 | |||||
| chr4:2732473
|
T | G | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*605T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 605 | chr4 | 2732473 | |||||
| chr4:2732474
|
T | A | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*606T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 21/21 | 606 | chr4 | 2732474 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:2537284
|
G | A | 3 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003 | 3 | HG01243.hp2 HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.255+114G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2537284 | ||||||
| chr4:2537330
|
C | T | 1 | a0001c0001t0002g0330 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.255+160C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2537330 | ||||||
| chr4:2537400
|
G | C | 1 | a0001c0001t0001g0004 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.255+230G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2537400 | ||||||
| chr4:2537618
|
C | T | 1 | a0001c0001t0002g0329 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.255+448C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2537618 | ||||||
| chr4:2537757
|
C | T | 1 | a0002c0012t0004g0328 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.255+587C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2537757 | ||||||
| chr4:2537848
|
G | A | 1 | a0006c0008t0001g0005 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.255+678G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2537848 | ||||||
| chr4:2537921
|
C | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+751C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2537921 | ||||||
| chr4:2538080
|
G | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+910G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2538080 | ||||||
| chr4:2538121
|
G | T | 1 | a0001c0001t0004g0316 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.255+951G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2538121 | ||||||
| chr4:2538122
|
T | G | 1 | a0001c0001t0004g0316 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.255+952T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2538122 | ||||||
| chr4:2538362
|
C | G | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG02015.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.255+1192C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2538362 | ||||||
| chr4:2538382
|
A | G | 1 | a0001c0002t0001g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.255+1212A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2538382 | ||||||
| chr4:2538419
|
G | C | 113 | a0001c0001t0001g0065a0001c0001t0002g0006a0001c0001t0002g0007others(110): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.255+1249G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2538419 | ||||||
| chr4:2538450
|
C | G | 75 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.255+1280C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2538450 | ||||||
| chr4:2538459
|
C | T | 5 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(2): Show | 5 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+1289C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2538459 | ||||||
| chr4:2538533
|
T | C | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.255+1363T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2538533 | ||||||
| chr4:2538564
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255+1394C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2538564 | ||||||
| chr4:2538672
|
C | T | 2 | a0001c0001t0001g0312a0001c0001t0001g0313 | 2 | HG01934.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.255+1502C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2538672 | ||||||
| chr4:2538768
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.255+1598A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2538768 | ||||||
| chr4:2538783
|
A | G | 1 | a0001c0001t0001g0311 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.255+1613A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2538783 | ||||||
| chr4:2538899
|
AT | A | 16 | a0001c0001t0001g0241a0001c0002t0001g0113a0001c0002t0003g0112others(13): Show | 16 | HG01516.hp1 HG01891.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.255+1738delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2538899 | |||||
| chr4:2538967
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.255+1797C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2538967 | ||||||
| chr4:2539000
|
C | T | 1 | a0010c0022t0001g0227 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.255+1830C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2539000 | ||||||
| chr4:2539057
|
A | C | 1 | a0002c0006t0002g0105 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.255+1887A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2539057 | ||||||
| chr4:2539103
|
A | T | 4 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(1): Show | 4 | HG02451.hp2 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+1933A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2539103 | ||||||
| chr4:2539370
|
A | T | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.255+2200A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2539370 | ||||||
| chr4:2539373
|
A | G | 1 | a0008c0009t0001g0310 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.255+2203A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2539373 | ||||||
| chr4:2539426
|
T | C | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG02015.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.255+2256T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2539426 | ||||||
| chr4:2539488
|
A | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.255+2318A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2539488 | ||||||
| chr4:2539557
|
C | G | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | NA18960.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.255+2387C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2539557 | ||||||
| chr4:2539920
|
ATGAAACC others(10): Show |
A | 1 | a0001c0001t0001g0220 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.255+2760_255+2776d others(19): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2539920 | |||||
| chr4:2540118
|
C | CA | 15 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0241others(12): Show | 15 | HG01243.hp2 HG02055.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.255+2964dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2540118 | |||||
| chr4:2540118
|
CA | C | 105 | a0001c0001t0001g0065a0001c0001t0001g0217a0001c0001t0001g0218others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.255+2964delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2540118 | |||||
| chr4:2540152
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.255+2982C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2540152 | ||||||
| chr4:2540194
|
G | A | 7 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(4): Show | 7 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.255+3024G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2540194 | ||||||
| chr4:2540257
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.255+3087C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2540257 | ||||||
| chr4:2540286
|
A | G | 1 | a0001c0001t0002g0009 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.255+3116A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2540286 | ||||||
| chr4:2540336
|
C | T | 76 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.255+3166C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2540336 | ||||||
| chr4:2540466
|
TCAAAA | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+3301_255+3305d others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2540466 | |||||
| chr4:2540541
|
C | G | 1 | a0001c0001t0001g0304 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.255+3371C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2540541 | ||||||
| chr4:2540605
|
G | A | 76 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.255+3435G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2540605 | ||||||
| chr4:2540817
|
C | T | 171 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.255+3647C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2540817 | ||||||
| chr4:2540954
|
G | C | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.255+3784G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2540954 | ||||||
| chr4:2540972
|
C | CA | 10 | a0001c0001t0001g0142a0001c0001t0001g0217a0001c0001t0001g0304others(7): Show | 10 | HG01175.hp2 HG01981.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.255+3818dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2540972 | |||||
| chr4:2540972
|
CA | C | 9 | a0001c0001t0001g0214a0001c0001t0001g0302a0001c0001t0001g0303others(6): Show | 9 | HG00609.hp2 HG01070.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+3818delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2540972 | |||||
| chr4:2540972
|
CAA | C | 12 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.255+3817_255+3818d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2540972 | |||||
| chr4:2540988
|
A | G | 1 | a0005c0005t0004g0141 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.255+3818A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2540988 | ||||||
| chr4:2541421
|
G | A | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.255+4251G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2541421 | ||||||
| chr4:2541446
|
C | CT | 18 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0304others(15): Show | 18 | HG01192.hp2 HG01884.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.255+4294dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2541446 | |||||
| chr4:2541446
|
CT | C | 26 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(23): Show | 26 | HG00140.hp1 HG01074.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.255+4294delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2541446 | |||||
| chr4:2541447
|
T | TTTTTTTT others(52): Show |
1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.255+4314_255+4315i others(61): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2541447 | |||||
| chr4:2541506
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+4336C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2541506 | ||||||
| chr4:2541823
|
C | T | 67 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(64): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.255+4653C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2541823 | ||||||
| chr4:2541938
|
CCTCCTGA others(12): Show |
C | 1 | a0008c0009t0001g0301 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.255+4775_255+4793d others(21): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2541938 | |||||
| chr4:2542101
|
C | T | 1 | a0001c0001t0002g0099 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.255+4931C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2542101 | ||||||
| chr4:2542106
|
C | T | 103 | a0001c0001t0001g0065a0001c0001t0002g0006a0001c0001t0002g0007others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.255+4936C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2542106 | ||||||
| chr4:2542381
|
C | G | 1 | a0001c0001t0001g0300 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.255+5211C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2542381 | ||||||
| chr4:2542384
|
T | C | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+5214T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2542384 | ||||||
| chr4:2542404
|
A | G | 5 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(2): Show | 5 | HG00673.hp1 HG02015.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.255+5234A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2542404 | ||||||
| chr4:2542545
|
T | A | 1 | a0001c0001t0002g0019 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.255+5375T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2542545 | ||||||
| chr4:2542757
|
G | T | 1 | a0001c0001t0002g0098 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.255+5587G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2542757 | ||||||
| chr4:2542817
|
G | A | 7 | a0007c0007t0001g0110a0007c0007t0003g0106a0007c0007t0003g0107others(4): Show | 7 | HG01891.hp1 HG02717.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.255+5647G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2542817 | ||||||
| chr4:2542825
|
C | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+5655C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2542825 | ||||||
| chr4:2542829
|
C | A | 1 | a0001c0001t0001g0147 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.255+5659C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2542829 | ||||||
| chr4:2542841
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.255+5671C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2542841 | ||||||
| chr4:2542893
|
C | T | 1 | a0005c0005t0002g0138 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.255+5723C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2542893 | ||||||
| chr4:2542967
|
A | G | 1 | a0001c0001t0007g0137 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.255+5797A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2542967 | ||||||
| chr4:2542983
|
G | A | 6 | a0001c0001t0002g0008a0001c0001t0002g0020a0001c0001t0002g0021others(3): Show | 6 | HG01106.hp1 HG02886.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.255+5813G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2542983 | ||||||
| chr4:2543094
|
C | CT | 116 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0145others(113): Show | 116 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.255+5936dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2543094 | |||||
| chr4:2543196
|
T | C | 1 | a0001c0002t0003g0112 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.255+6026T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2543196 | ||||||
| chr4:2543268
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.255+6098T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2543268 | ||||||
| chr4:2543379
|
T | G | 1 | a0001c0001t0001g0201 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.255+6209T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2543379 | ||||||
| chr4:2543508
|
G | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.255+6338G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2543508 | ||||||
| chr4:2543529
|
C | T | 103 | a0001c0001t0001g0065a0001c0001t0002g0006a0001c0001t0002g0007others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.255+6359C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2543529 | ||||||
| chr4:2543608
|
G | A | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0329 | 3 | HG01106.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.255+6438G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2543608 | ||||||
| chr4:2543801
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+6631C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2543801 | ||||||
| chr4:2543817
|
C | G | 1 | a0001c0001t0001g0200 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.255+6647C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2543817 | ||||||
| chr4:2543869
|
C | CA | 7 | a0001c0001t0001g0251a0001c0001t0002g0029a0001c0001t0002g0094others(4): Show | 7 | HG01168.hp1 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.255+6725dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2543869 | |||||
| chr4:2543869
|
C | CAA | 41 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0017others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.255+6724_255+6725d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2543869 | |||||
| chr4:2543869
|
C | CAAA | 47 | a0001c0001t0001g0065a0001c0001t0002g0008a0001c0001t0002g0009others(44): Show | 47 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.255+6723_255+6725d others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2543869 | |||||
| chr4:2543869
|
C | CAAAA | 9 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0010others(6): Show | 9 | HG00438.hp2 HG01934.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+6722_255+6725d others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2543869 | |||||
| chr4:2543869
|
CA | C | 64 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0001t0001g0150others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.255+6725delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2543869 | |||||
| chr4:2543869
|
CAA | C | 41 | a0001c0001t0001g0142a0001c0001t0001g0152a0001c0001t0001g0153others(38): Show | 41 | HG00558.hp1 HG00642.hp1 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.255+6724_255+6725d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2543869 | |||||
| chr4:2543869
|
CAAA | C | 63 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0144others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.255+6723_255+6725d others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2543869 | |||||
| chr4:2543895
|
A | C | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+6725A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2543895 | ||||||
| chr4:2543919
|
C | T | 4 | a0004c0004t0001g0321a0004c0004t0003g0317a0004c0004t0003g0319others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+6749C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2543919 | ||||||
| chr4:2543946
|
G | A | 5 | a0001c0001t0001g0252a0001c0001t0001g0271a0001c0001t0001g0272others(2): Show | 5 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(2): Show |
intron_variant | MODIFIER | c.255+6776G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2543946 | ||||||
| chr4:2544138
|
A | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+6968A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2544138 | ||||||
| chr4:2544181
|
C | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.255+7011C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2544181 | ||||||
| chr4:2544236
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.255+7066A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2544236 | ||||||
| chr4:2544260
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255+7090T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2544260 | ||||||
| chr4:2544284
|
G | A | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.255+7114G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2544284 | ||||||
| chr4:2544358
|
A | G | 1 | a0004c0004t0001g0321 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.255+7188A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2544358 | ||||||
| chr4:2544547
|
C | CA | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.255+7384dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2544547 | |||||
| chr4:2544606
|
A | G | 5 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0166others(2): Show | 5 | HG00639.hp1 HG01175.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.255+7436A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2544606 | ||||||
| chr4:2544894
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.255+7724G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2544894 | ||||||
| chr4:2544907
|
T | A | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.255+7737T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2544907 | ||||||
| chr4:2544937
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.255+7767G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2544937 | ||||||
| chr4:2545061
|
C | T | 5 | a0001c0001t0001g0165a0001c0001t0001g0197a0001c0001t0001g0198others(2): Show | 5 | HG00738.hp2 HG01257.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+7891C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545061 | ||||||
| chr4:2545078
|
T | C | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.255+7908T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545078 | ||||||
| chr4:2545167
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.255+7997A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545167 | ||||||
| chr4:2545169
|
T | G | 1 | a0001c0001t0002g0033 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.255+7999T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545169 | ||||||
| chr4:2545212
|
T | C | 1 | a0001c0001t0002g0034 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.255+8042T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545212 | ||||||
| chr4:2545310
|
AGAACAAG others(6): Show |
A | 1 | a0001c0001t0001g0307 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.255+8141_255+8153d others(15): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545310 | ||||||
| chr4:2545392
|
A | AT | 103 | a0001c0001t0001g0065a0001c0001t0002g0006a0001c0001t0002g0007others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.255+8232dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2545392 | |||||
| chr4:2545508
|
A | G | 103 | a0001c0001t0001g0065a0001c0001t0002g0006a0001c0001t0002g0007others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.255+8338A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545508 | ||||||
| chr4:2545534
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.255+8364G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545534 | ||||||
| chr4:2545687
|
A | T | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.255+8517A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545687 | ||||||
| chr4:2545693
|
A | T | 2 | a0002c0014t0001g0270a0008c0009t0001g0295 | 2 | NA18947.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.255+8523A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545693 | ||||||
| chr4:2545737
|
A | C | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.255+8567A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545737 | ||||||
| chr4:2545804
|
C | T | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.255+8634C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545804 | ||||||
| chr4:2545877
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.255+8707C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545877 | ||||||
| chr4:2545884
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.255+8714T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545884 | ||||||
| chr4:2545890
|
C | G | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.255+8720C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545890 | ||||||
| chr4:2545898
|
C | G | 1 | a0001c0001t0002g0097 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.255+8728C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545898 | ||||||
| chr4:2545923
|
G | C | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.255+8753G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545923 | ||||||
| chr4:2545924
|
C | G | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.255+8754C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2545924 | ||||||
| chr4:2546123
|
G | T | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.255+8953G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2546123 | ||||||
| chr4:2546159
|
A | T | 90 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(87): Show | 90 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.255+8989A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2546159 | ||||||
| chr4:2546159
|
AT | A | 30 | a0001c0001t0002g0007a0001c0002t0001g0001a0001c0002t0001g0002others(27): Show | 30 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.255+9002delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2546159 | |||||
| chr4:2546200
|
C | T | 3 | a0005c0005t0004g0130a0005c0005t0004g0136a0005c0005t0007g0131 | 3 | HG01975.hp2 HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.255+9030C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2546200 | ||||||
| chr4:2546308
|
A | G | 1 | a0002c0006t0002g0102 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.255+9138A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2546308 | ||||||
| chr4:2546436
|
AAGTCTTG others(2): Show |
A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+9269_255+9277d others(11): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2546436 | |||||
| chr4:2546591
|
C | A | 1 | a0006c0008t0001g0132 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.255+9421C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2546591 | ||||||
| chr4:2546644
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.255+9474A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2546644 | ||||||
| chr4:2546657
|
T | A | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.255+9487T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2546657 | ||||||
| chr4:2546925
|
A | G | 7 | a0007c0007t0001g0110a0007c0007t0003g0106a0007c0007t0003g0107others(4): Show | 7 | HG01891.hp1 HG02717.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.255+9755A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2546925 | ||||||
| chr4:2547112
|
G | C | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.255+9942G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2547112 | ||||||
| chr4:2547381
|
G | A | 1 | a0008c0009t0001g0310 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.255+10211G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2547381 | ||||||
| chr4:2547498
|
C | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+10328C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2547498 | ||||||
| chr4:2547507
|
T | G | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.255+10337T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2547507 | ||||||
| chr4:2547529
|
C | T | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.255+10359C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2547529 | ||||||
| chr4:2547604
|
C | CTG | 26 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0001t0007g0129others(23): Show | 26 | HG00408.hp1 HG00609.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.255+10454_255+1045 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2547604 | |||||
| chr4:2547604
|
C | CTGTG | 5 | a0006c0008t0001g0127a0006c0008t0001g0132a0006c0008t0001g0216others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.255+10452_255+1045 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2547604 | |||||
| chr4:2547604
|
C | CTGTGTGT others(13): Show |
9 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(6): Show | 9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.255+10451_255+1045 others(24): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2547604 | |||||
| chr4:2547604
|
C | CTGTGTGT others(15): Show |
2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.255+10451_255+1045 others(26): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2547604 | |||||
| chr4:2547626
|
A | G | 10 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0220others(7): Show | 10 | HG00544.hp1 NA18612.hp1 NA18940.hp2 others(7): Show |
intron_variant | MODIFIER | c.255+10456A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2547626 | ||||||
| chr4:2547642
|
T | G | 1 | a0011c0023t0001g0247 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.255+10472T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2547642 | ||||||
| chr4:2547692
|
C | T | 101 | a0001c0001t0001g0065a0001c0001t0002g0006a0001c0001t0002g0007others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.255+10522C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2547692 | ||||||
| chr4:2547865
|
T | C | 1 | a0001c0001t0002g0035 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.255+10695T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2547865 | ||||||
| chr4:2547890
|
G | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.255+10720G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2547890 | ||||||
| chr4:2548040
|
T | C | 7 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0066others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.255+10870T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2548040 | ||||||
| chr4:2548071
|
A | AT | 14 | a0001c0001t0001g0185a0001c0001t0001g0202a0001c0001t0001g0217others(11): Show | 14 | HG01081.hp2 HG01981.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.255+10919dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2548071 | |||||
| chr4:2548071
|
AT | A | 182 | a0001c0001t0001g0065a0001c0001t0001g0214a0001c0001t0001g0221others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.255+10919delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2548071 | |||||
| chr4:2548245
|
A | G | 1 | a0006c0008t0001g0132 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.255+11075A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2548245 | ||||||
| chr4:2548272
|
T | C | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.255+11102T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2548272 | ||||||
| chr4:2548381
|
A | G | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | NA18960.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.255+11211A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2548381 | ||||||
| chr4:2548404
|
T | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+11234T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2548404 | ||||||
| chr4:2548493
|
G | A | 1 | a0001c0001t0001g0275 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.255+11323G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2548493 | ||||||
| chr4:2548515
|
G | A | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.255+11345G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2548515 | ||||||
| chr4:2548611
|
C | T | 2 | a0007c0007t0003g0106a0007c0007t0003g0107 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.255+11441C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2548611 | ||||||
| chr4:2548612
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.255+11442G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2548612 | ||||||
| chr4:2548745
|
C | T | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.255+11575C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2548745 | ||||||
| chr4:2549076
|
TA | T | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.255+11908delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2549076 | |||||
| chr4:2549180
|
G | T | 3 | a0004c0004t0001g0318a0004c0004t0001g0322a0004c0017t0001g0324 | 3 | HG02258.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.255+12010G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2549180 | ||||||
| chr4:2549230
|
A | T | 1 | a0001c0001t0001g0167 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.255+12060A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2549230 | ||||||
| chr4:2549309
|
T | C | 1 | a0001c0001t0002g0070 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.255+12139T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2549309 | ||||||
| chr4:2549337
|
G | A | 2 | a0004c0004t0001g0323a0004c0004t0001g0327 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.255+12167G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2549337 | ||||||
| chr4:2549395
|
C | CT | 30 | a0001c0001t0001g0152a0001c0001t0001g0184a0001c0001t0001g0231others(27): Show | 30 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.255+12244dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2549395 | |||||
| chr4:2549395
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.255+12225C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2549395 | ||||||
| chr4:2549400
|
T | C | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.255+12230T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2549400 | ||||||
| chr4:2549401
|
T | C | 1 | a0001c0001t0002g0030 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.255+12231T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2549401 | ||||||
| chr4:2549465
|
C | T | 2 | a0001c0001t0001g0312a0001c0001t0001g0313 | 2 | HG01934.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.255+12295C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2549465 | ||||||
| chr4:2549556
|
T | C | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.255+12386T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2549556 | ||||||
| chr4:2549557
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.255+12387C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2549557 | ||||||
| chr4:2549597
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.255+12427C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2549597 | ||||||
| chr4:2549618
|
G | A | 1 | a0003c0003t0004g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.255+12448G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2549618 | ||||||
| chr4:2549648
|
A | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+12478A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2549648 | ||||||
| chr4:2549931
|
A | G | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.255+12761A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2549931 | ||||||
| chr4:2550025
|
C | CT | 102 | a0001c0001t0001g0065a0001c0001t0001g0206a0001c0001t0001g0309others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.255+12871dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2550025 | |||||
| chr4:2550065
|
G | C | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+12895G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550065 | ||||||
| chr4:2550068
|
G | C | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.255+12898G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550068 | ||||||
| chr4:2550295
|
C | G | 1 | a0001c0001t0002g0013 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.255+13125C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550295 | ||||||
| chr4:2550326
|
G | A | 101 | a0001c0001t0001g0065a0001c0001t0002g0006a0001c0001t0002g0007others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.255+13156G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550326 | ||||||
| chr4:2550355
|
T | A | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.255+13185T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550355 | ||||||
| chr4:2550357
|
A | T | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.255+13187A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550357 | ||||||
| chr4:2550360
|
C | T | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.255+13190C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550360 | ||||||
| chr4:2550444
|
GTTTA | G | 4 | a0001c0001t0001g0163a0001c0001t0001g0181a0001c0001t0001g0182others(1): Show | 4 | NA18945.hp2 NA18983.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+13278_255+1328 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2550444 | |||||
| chr4:2550448
|
A | G | 287 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.255+13278A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550448 | ||||||
| chr4:2550499
|
C | T | 6 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0179others(3): Show | 6 | HG01256.hp2 HG01258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+13329C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550499 | ||||||
| chr4:2550505
|
T | C | 323 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(320): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.255+13335T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550505 | ||||||
| chr4:2550529
|
C | T | 1 | a0003c0003t0004g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.255+13359C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550529 | ||||||
| chr4:2550771
|
TTTTA | T | 41 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(38): Show | 41 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.255+13646_255+1364 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2550771 | |||||
| chr4:2550771
|
TTTTATTT others(1): Show |
T | 26 | a0001c0001t0001g0254a0001c0001t0001g0267a0001c0001t0001g0293others(23): Show | 26 | HG00673.hp1 HG01074.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.255+13642_255+1364 others(12): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2550771 | |||||
| chr4:2550771
|
TTTTATTT others(5): Show |
T | 113 | a0001c0001t0001g0065a0001c0001t0001g0152a0001c0001t0001g0231others(110): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.255+13638_255+1364 others(16): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2550771 | |||||
| chr4:2550771
|
TTTTATTT others(9): Show |
T | 16 | a0001c0001t0001g0133a0001c0001t0001g0253a0001c0002t0003g0116others(13): Show | 16 | HG01167.hp1 HG02132.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.255+13634_255+1364 others(20): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2550771 | |||||
| chr4:2550771
|
TTTTATTT others(13): Show |
T | 87 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(84): Show | 87 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.255+13630_255+1364 others(24): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2550771 | |||||
| chr4:2550780
|
T | G | 12 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(9): Show | 12 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.255+13610T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550780 | ||||||
| chr4:2550781
|
T | G | 1 | a0001c0001t0002g0036 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.255+13611T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550781 | ||||||
| chr4:2550784
|
T | G | 6 | a0001c0002t0001g0113a0001c0002t0003g0112a0001c0002t0003g0120others(3): Show | 6 | HG01516.hp1 HG02615.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+13614T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550784 | ||||||
| chr4:2550788
|
T | G | 2 | a0001c0002t0003g0116a0001c0002t0003g0119 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.255+13618T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550788 | ||||||
| chr4:2550843
|
C | G | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.255+13673C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550843 | ||||||
| chr4:2550865
|
A | T | 1 | a0001c0001t0001g0147 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.255+13695A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550865 | ||||||
| chr4:2550893
|
C | T | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | HG02004.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.255+13723C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550893 | ||||||
| chr4:2550942
|
A | C | 1 | a0001c0001t0001g0303 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.255+13772A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550942 | ||||||
| chr4:2550985
|
A | G | 1 | a0006c0008t0001g0121 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.255+13815A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2550985 | ||||||
| chr4:2551025
|
C | T | 1 | a0001c0001t0002g0035 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.255+13855C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2551025 | ||||||
| chr4:2551063
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+13893G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2551063 | ||||||
| chr4:2551084
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.255+13914G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2551084 | ||||||
| chr4:2551389
|
A | G | 2 | a0001c0001t0001g0282a0001c0001t0001g0296 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.255+14219A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2551389 | ||||||
| chr4:2551518
|
C | T | 3 | a0006c0008t0001g0127a0006c0008t0001g0132a0006c0008t0001g0216 | 3 | HG02818.hp1 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.255+14348C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2551518 | ||||||
| chr4:2551587
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255+14417T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2551587 | ||||||
| chr4:2551644
|
T | C | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.255+14474T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2551644 | ||||||
| chr4:2551672
|
T | C | 13 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0001t0007g0129others(10): Show | 13 | HG00408.hp1 HG01074.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.255+14502T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2551672 | ||||||
| chr4:2551753
|
G | GT | 6 | a0001c0001t0001g0147a0001c0001t0001g0212a0001c0001t0002g0062others(3): Show | 6 | HG02080.hp1 NA18967.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.255+14588dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2551753 | |||||
| chr4:2551777
|
A | G | 6 | a0001c0001t0002g0017a0001c0001t0002g0032a0001c0001t0002g0033others(3): Show | 6 | HG00558.hp2 HG01074.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+14607A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2551777 | ||||||
| chr4:2551821
|
G | T | 1 | a0007c0007t0003g0107 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.255+14651G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2551821 | ||||||
| chr4:2552008
|
A | AT | 274 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.255+14858dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2552008 | |||||
| chr4:2552008
|
A | ATT | 34 | a0001c0001t0001g0151a0001c0001t0001g0178a0001c0001t0001g0214others(31): Show | 34 | HG01099.hp1 HG01106.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.255+14857_255+1485 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2552008 | |||||
| chr4:2552063
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+14893G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2552063 | ||||||
| chr4:2552091
|
A | G | 1 | a0001c0001t0002g0015 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.255+14921A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2552091 | ||||||
| chr4:2552130
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.255+14960G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2552130 | ||||||
| chr4:2552210
|
A | G | 3 | a0004c0004t0001g0318a0004c0004t0001g0322a0004c0017t0001g0324 | 3 | HG02258.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.255+15040A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2552210 | ||||||
| chr4:2552235
|
C | T | 223 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0123others(220): Show | 223 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.255+15065C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2552235 | ||||||
| chr4:2552307
|
G | A | 5 | a0001c0001t0001g0165a0001c0001t0001g0197a0001c0001t0001g0198others(2): Show | 5 | HG00738.hp2 HG01257.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+15137G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2552307 | ||||||
| chr4:2552312
|
AT | A | 323 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(320): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.255+15151delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2552312 | |||||
| chr4:2552430
|
C | T | 101 | a0001c0001t0001g0065a0001c0001t0002g0006a0001c0001t0002g0007others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.255+15260C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2552430 | ||||||
| chr4:2552474
|
C | G | 1 | a0001c0001t0002g0032 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.255+15304C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2552474 | ||||||
| chr4:2552495
|
A | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.255+15325A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2552495 | ||||||
| chr4:2552551
|
T | G | 2 | a0007c0007t0003g0106a0007c0007t0003g0107 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.255+15381T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2552551 | ||||||
| chr4:2552569
|
C | T | 75 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.255+15399C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2552569 | ||||||
| chr4:2552738
|
C | T | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.255+15568C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2552738 | ||||||
| chr4:2552842
|
A | AATTT | 3 | a0004c0004t0001g0323a0004c0004t0001g0327a0004c0004t0003g0320 | 3 | HG02145.hp1 HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.255+15672_255+1567 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2552842 | ||||||
| chr4:2552843
|
C | A | 8 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(5): Show | 8 | HG02257.hp1 HG02258.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.255+15673C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2552843 | ||||||
| chr4:2552847
|
C | CT | 95 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0123others(92): Show | 95 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.255+15697dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2552847 | |||||
| chr4:2552847
|
C | CTT | 6 | a0001c0001t0001g0142a0002c0012t0004g0328a0003c0003t0005g0164others(3): Show | 6 | HG02257.hp2 HG02970.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.255+15696_255+1569 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2552847 | |||||
| chr4:2552847
|
C | CTTT | 8 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(5): Show | 8 | HG02257.hp1 HG02258.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.255+15695_255+1569 others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2552847 | |||||
| chr4:2552847
|
C | T | 3 | a0004c0004t0001g0323a0004c0004t0001g0327a0004c0004t0003g0320 | 3 | HG02145.hp1 HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.255+15677C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2552847 | ||||||
| chr4:2552847
|
CT | C | 29 | a0001c0001t0001g0293a0001c0001t0001g0296a0001c0001t0002g0032others(26): Show | 29 | HG00738.hp1 HG01081.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.255+15697delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2552847 | |||||
| chr4:2552851
|
T | C | 1 | a0001c0001t0006g0042 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.255+15681T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2552851 | ||||||
| chr4:2553008
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.255+15838C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2553008 | ||||||
| chr4:2553124
|
G | A | 2 | a0004c0004t0001g0318a0004c0004t0001g0322 | 2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.255+15954G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2553124 | ||||||
| chr4:2553196
|
G | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0265 | 2 | NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.255+16026G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2553196 | ||||||
| chr4:2553367
|
A | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.255+16197A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2553367 | ||||||
| chr4:2553376
|
C | CT | 7 | a0001c0001t0001g0252a0001c0001t0001g0264a0001c0001t0001g0273others(4): Show | 7 | HG00733.hp1 HG00735.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.255+16211dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2553376 | |||||
| chr4:2553381
|
TG | T | 10 | a0001c0001t0001g0241a0001c0001t0001g0271a0001c0001t0001g0283others(7): Show | 10 | HG00323.hp1 HG02004.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.255+16212delG | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2553381 | ||||||
| chr4:2553382
|
G | GT | 14 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0030others(11): Show | 14 | HG00438.hp2 HG00609.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.255+16229dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2553382 | |||||
| chr4:2553382
|
G | T | 64 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.255+16212G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2553382 | ||||||
| chr4:2553382
|
GT | G | 192 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(189): Show | 192 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.255+16229delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2553382 | |||||
| chr4:2553382
|
GTT | G | 10 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.255+16228_255+1622 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2553382 | |||||
| chr4:2553383
|
T | G | 1 | a0001c0001t0002g0015 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.255+16213T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2553383 | ||||||
| chr4:2553636
|
T | C | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.255+16466T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2553636 | ||||||
| chr4:2553651
|
T | A | 1 | a0001c0002t0013g0117 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.255+16481T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2553651 | ||||||
| chr4:2553659
|
G | A | 2 | a0004c0004t0001g0323a0004c0004t0001g0327 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.255+16489G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2553659 | ||||||
| chr4:2553682
|
T | A | 2 | a0001c0001t0001g0312a0001c0001t0001g0313 | 2 | HG01934.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.255+16512T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2553682 | ||||||
| chr4:2554058
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.255+16888G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2554058 | ||||||
| chr4:2554082
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.255+16912C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2554082 | ||||||
| chr4:2554189
|
G | A | 33 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(30): Show | 33 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.255+17019G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2554189 | ||||||
| chr4:2554271
|
G | T | 1 | a0001c0001t0001g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.255+17101G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2554271 | ||||||
| chr4:2554287
|
G | T | 1 | a0001c0001t0001g0251 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.255+17117G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2554287 | ||||||
| chr4:2554331
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+17161G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2554331 | ||||||
| chr4:2554360
|
G | A | 2 | a0008c0009t0001g0266a0008c0009t0001g0301 | 2 | NA18944.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.255+17190G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2554360 | ||||||
| chr4:2554374
|
G | C | 76 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.255+17204G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2554374 | ||||||
| chr4:2554380
|
G | A | 9 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(6): Show | 9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.255+17210G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2554380 | ||||||
| chr4:2554522
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.255+17352A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2554522 | ||||||
| chr4:2554540
|
A | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+17370A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2554540 | ||||||
| chr4:2554634
|
T | G | 1 | a0001c0001t0002g0015 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.255+17464T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2554634 | ||||||
| chr4:2554745
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.255+17575G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2554745 | ||||||
| chr4:2554882
|
T | G | 2 | a0001c0001t0002g0075a0001c0001t0002g0100 | 2 | HG02056.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.255+17712T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2554882 | ||||||
| chr4:2554951
|
A | G | 3 | a0001c0001t0002g0036a0001c0001t0002g0067a0001c0001t0002g0068 | 3 | HG01070.hp2 HG01071.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.255+17781A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2554951 | ||||||
| chr4:2555070
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.255+17900C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2555070 | ||||||
| chr4:2555174
|
C | T | 14 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0001t0007g0129others(11): Show | 14 | HG00408.hp1 HG01074.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.255+18004C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2555174 | ||||||
| chr4:2555230
|
T | C | 1 | a0003c0003t0004g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.255+18060T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2555230 | ||||||
| chr4:2555476
|
T | C | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | NA18960.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.255+18306T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2555476 | ||||||
| chr4:2555562
|
T | G | 1 | a0001c0001t0002g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.255+18392T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2555562 | ||||||
| chr4:2555635
|
TGAGA | T | 9 | a0001c0001t0002g0035a0001c0001t0002g0039a0001c0001t0002g0054others(6): Show | 9 | HG01928.hp1 NA18612.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+18466_255+1846 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2555635 | ||||||
| chr4:2555636
|
G | C | 93 | a0001c0001t0001g0065a0001c0001t0002g0006a0001c0001t0002g0007others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.255+18466G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2555636 | ||||||
| chr4:2555659
|
T | C | 33 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(30): Show | 33 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.255+18489T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2555659 | ||||||
| chr4:2555698
|
A | G | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.255+18528A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2555698 | ||||||
| chr4:2555793
|
AT | A | 89 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(86): Show | 89 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.255+18628delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2555793 | |||||
| chr4:2555795
|
T | C | 1 | a0001c0001t0002g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.255+18625T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2555795 | ||||||
| chr4:2555858
|
C | T | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.255+18688C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2555858 | ||||||
| chr4:2555868
|
G | A | 1 | a0003c0003t0011g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.255+18698G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2555868 | ||||||
| chr4:2555908
|
G | GT | 18 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0001t0001g0259others(15): Show | 18 | HG00408.hp1 HG01074.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.255+18751dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2555908 | |||||
| chr4:2555974
|
G | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+18804G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2555974 | ||||||
| chr4:2556120
|
G | A | 10 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0259others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.255+18950G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2556120 | ||||||
| chr4:2556139
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.255+18969G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2556139 | ||||||
| chr4:2556176
|
A | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+19006A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2556176 | ||||||
| chr4:2556185
|
T | C | 1 | a0007c0007t0003g0111 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.255+19015T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2556185 | ||||||
| chr4:2556331
|
G | A | 2 | a0004c0004t0001g0318a0004c0004t0001g0322 | 2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.255+19161G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2556331 | ||||||
| chr4:2556331
|
G | T | 102 | a0001c0001t0001g0065a0001c0001t0002g0006a0001c0001t0002g0007others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.255+19161G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2556331 | ||||||
| chr4:2556574
|
C | T | 5 | a0003c0003t0005g0164a0003c0003t0005g0187a0003c0003t0005g0188others(2): Show | 5 | HG02257.hp2 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.255+19404C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2556574 | ||||||
| chr4:2556622
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0291 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.255+19452C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2556622 | ||||||
| chr4:2556759
|
T | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+19589T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2556759 | ||||||
| chr4:2556777
|
G | C | 166 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.255+19607G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2556777 | ||||||
| chr4:2556780
|
T | C | 1 | a0001c0001t0002g0086 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.255+19610T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2556780 | ||||||
| chr4:2556787
|
C | T | 1 | a0001c0001t0002g0070 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.255+19617C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2556787 | ||||||
| chr4:2557176
|
C | A | 76 | a0001c0001t0001g0004a0001c0001t0001g0241a0001c0001t0001g0243others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.255+20006C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2557176 | ||||||
| chr4:2557226
|
A | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0175 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.255+20056A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2557226 | ||||||
| chr4:2557314
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.255+20144G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2557314 | ||||||
| chr4:2557382
|
C | T | 1 | a0001c0001t0002g0009 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.255+20212C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2557382 | ||||||
| chr4:2557588
|
C | T | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.255+20418C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2557588 | ||||||
| chr4:2557605
|
A | G | 1 | a0001c0001t0002g0085 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.255+20435A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2557605 | ||||||
| chr4:2557698
|
A | G | 1 | a0001c0002t0003g0112 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.255+20528A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2557698 | ||||||
| chr4:2557731
|
T | G | 1 | a0003c0003t0001g0236 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.255+20561T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2557731 | ||||||
| chr4:2557748
|
C | A | 1 | a0001c0001t0002g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.255+20578C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2557748 | ||||||
| chr4:2557811
|
G | A | 2 | a0001c0001t0007g0129a0001c0001t0007g0137 | 2 | HG01167.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.255+20641G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2557811 | ||||||
| chr4:2557881
|
G | C | 1 | a0001c0001t0001g0218 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.255+20711G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2557881 | ||||||
| chr4:2558039
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.255+20869G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2558039 | ||||||
| chr4:2558083
|
G | A | 1 | a0001c0001t0006g0016 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.255+20913G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2558083 | ||||||
| chr4:2558144
|
T | C | 56 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(53): Show | 56 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.255+20974T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2558144 | ||||||
| chr4:2558195
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.255+21025C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2558195 | ||||||
| chr4:2558201
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.255+21031G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2558201 | ||||||
| chr4:2558228
|
T | A | 89 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(86): Show | 89 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.255+21058T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2558228 | ||||||
| chr4:2558263
|
C | T | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.255+21093C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2558263 | ||||||
| chr4:2558273
|
GA | G | 7 | a0001c0001t0001g0144a0001c0001t0001g0160a0001c0001t0001g0174others(4): Show | 7 | HG03453.hp2 NA18947.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.255+21117delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2558273 | |||||
| chr4:2558274
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.255+21104A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2558274 | ||||||
| chr4:2558383
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.255+21213A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2558383 | ||||||
| chr4:2558566
|
G | T | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.255+21396G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2558566 | ||||||
| chr4:2558641
|
G | A | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.255+21471G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2558641 | ||||||
| chr4:2558694
|
C | T | 2 | a0006c0008t0001g0125a0006c0008t0001g0126 | 2 | HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.255+21524C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2558694 | ||||||
| chr4:2558758
|
C | T | 2 | a0001c0001t0008g0249a0011c0023t0001g0247 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.255+21588C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2558758 | ||||||
| chr4:2558952
|
A | G | 6 | a0006c0008t0001g0121a0006c0008t0001g0125a0006c0008t0001g0126others(3): Show | 6 | HG02559.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+21782A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2558952 | ||||||
| chr4:2559091
|
G | A | 6 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0179others(3): Show | 6 | HG01256.hp2 HG01258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+21921G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2559091 | ||||||
| chr4:2559226
|
C | T | 3 | a0001c0001t0002g0072a0001c0001t0002g0074a0002c0006t0002g0105 | 3 | HG00738.hp1 HG01081.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.255+22056C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2559226 | ||||||
| chr4:2559228
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.255+22058G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2559228 | ||||||
| chr4:2559244
|
C | T | 2 | a0001c0001t0002g0022a0001c0002t0016g0023 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.255+22074C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2559244 | ||||||
| chr4:2559342
|
G | A | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.255+22172G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2559342 | ||||||
| chr4:2559484
|
G | T | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.255+22314G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2559484 | ||||||
| chr4:2559512
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.255+22342A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2559512 | ||||||
| chr4:2559535
|
A | G | 13 | a0001c0001t0001g0122a0001c0001t0006g0016a0001c0001t0007g0129others(10): Show | 13 | HG01074.hp1 HG01167.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.255+22365A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2559535 | ||||||
| chr4:2559626
|
C | T | 2 | a0001c0001t0001g0223a0001c0025t0001g0224 | 2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.255+22456C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2559626 | ||||||
| chr4:2559692
|
G | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0231a0001c0001t0001g0232 | 3 | HG02647.hp1 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255+22522G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2559692 | ||||||
| chr4:2559712
|
C | T | 1 | a0006c0008t0001g0121 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.255+22542C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2559712 | ||||||
| chr4:2559802
|
C | T | 2 | a0004c0004t0001g0323a0004c0004t0001g0327 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.255+22632C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2559802 | ||||||
| chr4:2559940
|
C | T | 4 | a0004c0004t0001g0321a0004c0004t0003g0317a0004c0004t0003g0319others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+22770C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2559940 | ||||||
| chr4:2559965
|
C | CT | 21 | a0001c0001t0001g0256a0001c0002t0001g0001a0001c0002t0001g0002others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.255+22805dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2559965 | |||||
| chr4:2560066
|
C | G | 1 | a0001c0001t0001g0147 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.255+22896C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2560066 | ||||||
| chr4:2560177
|
A | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+23007A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2560177 | ||||||
| chr4:2560248
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.255+23078A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2560248 | ||||||
| chr4:2560251
|
C | G | 268 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0123others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.255+23081C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2560251 | ||||||
| chr4:2560348
|
C | T | 1 | a0001c0001t0002g0053 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.255+23178C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2560348 | ||||||
| chr4:2560360
|
G | T | 2 | a0001c0001t0001g0255a0002c0006t0001g0242 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.255+23190G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2560360 | ||||||
| chr4:2560681
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+23511G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2560681 | ||||||
| chr4:2560804
|
C | G | 1 | a0001c0001t0001g0147 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.255+23634C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2560804 | ||||||
| chr4:2560932
|
C | G | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.255+23762C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2560932 | ||||||
| chr4:2561015
|
G | A | 2 | a0001c0001t0002g0022a0001c0002t0016g0023 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.255+23845G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2561015 | ||||||
| chr4:2561053
|
C | G | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.255+23883C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2561053 | ||||||
| chr4:2561066
|
C | T | 11 | a0001c0001t0001g0122a0001c0001t0001g0133a0002c0012t0004g0328others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+23896C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2561066 | ||||||
| chr4:2561080
|
G | A | 87 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(84): Show | 87 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.255+23910G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2561080 | ||||||
| chr4:2561083
|
A | C | 1 | a0001c0001t0001g0293 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.255+23913A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2561083 | ||||||
| chr4:2561109
|
C | A | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.255+23939C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2561109 | ||||||
| chr4:2561250
|
A | G | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.255+24080A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2561250 | ||||||
| chr4:2561408
|
C | T | 5 | a0001c0001t0002g0012a0001c0001t0002g0029a0001c0001t0002g0084others(2): Show | 5 | HG01168.hp1 HG01175.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+24238C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2561408 | ||||||
| chr4:2561442
|
C | G | 1 | a0001c0001t0002g0083 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.255+24272C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2561442 | ||||||
| chr4:2561497
|
C | CT | 78 | a0001c0001t0001g0122a0001c0001t0001g0184a0001c0001t0001g0231others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.255+24344dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2561497 | |||||
| chr4:2561523
|
G | C | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+24353G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2561523 | ||||||
| chr4:2561568
|
C | A | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.255+24398C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2561568 | ||||||
| chr4:2561621
|
C | T | 1 | a0001c0001t0004g0208 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.255+24451C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2561621 | ||||||
| chr4:2561673
|
G | T | 33 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(30): Show | 33 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.255+24503G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2561673 | ||||||
| chr4:2561685
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.255+24515C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2561685 | ||||||
| chr4:2561697
|
G | A | 1 | a0001c0001t0004g0196 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.255+24527G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2561697 | ||||||
| chr4:2561918
|
G | C | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.255+24748G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2561918 | ||||||
| chr4:2561981
|
T | C | 1 | a0001c0001t0001g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.255+24811T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2561981 | ||||||
| chr4:2562096
|
C | G | 1 | a0001c0001t0001g0272 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.255+24926C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2562096 | ||||||
| chr4:2562334
|
C | A | 1 | a0001c0001t0012g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.255+25164C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2562334 | ||||||
| chr4:2562470
|
C | T | 17 | a0001c0001t0001g0004a0001c0001t0001g0145a0001c0001t0001g0146others(14): Show | 17 | HG00558.hp1 HG00609.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.255+25300C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2562470 | ||||||
| chr4:2562482
|
A | G | 2 | a0001c0001t0006g0042a0001c0001t0006g0052 | 2 | NA18747.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.255+25312A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2562482 | ||||||
| chr4:2562485
|
C | G | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.255+25315C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2562485 | ||||||
| chr4:2562505
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.255+25335C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2562505 | ||||||
| chr4:2562514
|
G | A | 1 | a0001c0001t0002g0053 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.255+25344G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2562514 | ||||||
| chr4:2562595
|
G | C | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.255+25425G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2562595 | ||||||
| chr4:2562636
|
G | GT | 26 | a0001c0001t0001g0258a0001c0001t0004g0316a0001c0002t0001g0001others(23): Show | 26 | HG01106.hp2 HG01243.hp2 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.255+25479dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2562636 | |||||
| chr4:2562665
|
C | T | 2 | a0006c0008t0001g0125a0006c0008t0001g0126 | 2 | HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.255+25495C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2562665 | ||||||
| chr4:2562706
|
C | T | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.255+25536C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2562706 | ||||||
| chr4:2562781
|
C | A | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.255+25611C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2562781 | ||||||
| chr4:2562810
|
A | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.255+25640A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2562810 | ||||||
| chr4:2562826
|
C | T | 2 | a0004c0004t0001g0323a0004c0004t0001g0327 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.255+25656C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2562826 | ||||||
| chr4:2562922
|
C | A | 13 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0021t0003g0143others(10): Show | 13 | HG00408.hp1 HG01074.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.255+25752C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2562922 | ||||||
| chr4:2562946
|
C | G | 1 | a0001c0001t0002g0031 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.255+25776C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2562946 | ||||||
| chr4:2562983
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.255+25813C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2562983 | ||||||
| chr4:2563009
|
A | G | 2 | a0004c0004t0001g0323a0004c0004t0001g0327 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.255+25839A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563009 | ||||||
| chr4:2563060
|
T | G | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.255+25890T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563060 | ||||||
| chr4:2563099
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.255+25929C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563099 | ||||||
| chr4:2563189
|
T | C | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.255+26019T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563189 | ||||||
| chr4:2563223
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+26053G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563223 | ||||||
| chr4:2563525
|
C | CA | 81 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0156others(78): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.255+26364dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2563525 | |||||
| chr4:2563530
|
A | G | 1 | a0001c0001t0002g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.255+26360A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563530 | ||||||
| chr4:2563536
|
A | G | 276 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0123others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.255+26366A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563536 | ||||||
| chr4:2563539
|
A | G | 1 | a0003c0003t0005g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.255+26369A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563539 | ||||||
| chr4:2563615
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.255+26445G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563615 | ||||||
| chr4:2563652
|
C | T | 33 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(30): Show | 33 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.255+26482C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563652 | ||||||
| chr4:2563684
|
A | G | 15 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0001t0007g0129others(12): Show | 15 | HG00408.hp1 HG01074.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.255+26514A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563684 | ||||||
| chr4:2563687
|
A | G | 1 | a0005c0005t0004g0136 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.255+26517A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563687 | ||||||
| chr4:2563709
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+26539C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563709 | ||||||
| chr4:2563714
|
C | T | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0329 | 3 | HG01106.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.255+26544C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563714 | ||||||
| chr4:2563777
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.255+26607G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563777 | ||||||
| chr4:2563834
|
C | T | 1 | a0001c0001t0002g0013 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.255+26664C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563834 | ||||||
| chr4:2563949
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+26779G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563949 | ||||||
| chr4:2563972
|
T | G | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.255+26802T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563972 | ||||||
| chr4:2563999
|
T | C | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.255+26829T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2563999 | ||||||
| chr4:2564362
|
T | C | 33 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(30): Show | 33 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.255+27192T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2564362 | ||||||
| chr4:2564449
|
C | T | 5 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(2): Show | 5 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+27279C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2564449 | ||||||
| chr4:2564592
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.255+27422A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2564592 | ||||||
| chr4:2564675
|
A | C | 1 | a0001c0001t0002g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.255+27505A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2564675 | ||||||
| chr4:2564896
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.255+27726C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2564896 | ||||||
| chr4:2565129
|
G | C | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+27959G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565129 | ||||||
| chr4:2565137
|
T | C | 1 | a0006c0008t0001g0124 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.255+27967T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565137 | ||||||
| chr4:2565254
|
C | CTTTT | 7 | a0001c0001t0001g0263a0001c0001t0001g0290a0006c0008t0001g0121others(4): Show | 7 | HG01516.hp2 HG01517.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.255+28103_255+2810 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2565254 | |||||
| chr4:2565254
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.255+28084C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565254 | ||||||
| chr4:2565276
|
T | A | 3 | a0001c0001t0002g0026a0009c0010t0014g0228a0009c0010t0015g0229 | 3 | HG00099.hp1 HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.255+28106T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565276 | ||||||
| chr4:2565276
|
T | TTTA | 13 | a0001c0001t0001g0244a0001c0001t0001g0246a0001c0001t0001g0250others(10): Show | 13 | HG01109.hp1 HG01168.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.255+28106_255+2810 others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565276 | ||||||
| chr4:2565276
|
T | TTTTA | 58 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0245others(55): Show | 58 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.255+28106_255+2810 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565276 | ||||||
| chr4:2565276
|
T | TTTTTA | 25 | a0001c0001t0001g0144a0001c0001t0001g0197a0001c0001t0001g0225others(22): Show | 25 | HG01070.hp2 HG01168.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.255+28106_255+2810 others(9): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565276 | ||||||
| chr4:2565276
|
T | TTTTTAAA | 12 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0113others(9): Show | 12 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.255+28106_255+2810 others(11): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565276 | ||||||
| chr4:2565276
|
T | TTTTTTA | 153 | a0001c0001t0001g0004a0001c0001t0001g0133a0001c0001t0001g0145others(150): Show | 153 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.255+28106_255+2810 others(10): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565276 | ||||||
| chr4:2565276
|
T | TTTTTTTA | 34 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0123others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.255+28106_255+2810 others(11): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565276 | ||||||
| chr4:2565343
|
T | A | 3 | a0006c0008t0001g0127a0006c0008t0001g0132a0006c0008t0001g0216 | 3 | HG02818.hp1 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.255+28173T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565343 | ||||||
| chr4:2565569
|
T | G | 104 | a0001c0001t0001g0065a0001c0001t0002g0006a0001c0001t0002g0007others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.255+28399T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565569 | ||||||
| chr4:2565574
|
T | TA | 11 | a0001c0001t0001g0142a0001c0001t0002g0015a0001c0001t0002g0017others(8): Show | 11 | HG00558.hp2 HG01074.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.255+28416dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2565574 | |||||
| chr4:2565591
|
T | C | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.255+28421T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565591 | ||||||
| chr4:2565616
|
G | A | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.255+28446G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565616 | ||||||
| chr4:2565728
|
A | G | 1 | a0001c0016t0001g0308 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.255+28558A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565728 | ||||||
| chr4:2565739
|
A | T | 6 | a0006c0008t0001g0121a0006c0008t0001g0125a0006c0008t0001g0126others(3): Show | 6 | HG02559.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+28569A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565739 | ||||||
| chr4:2565788
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255+28618C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565788 | ||||||
| chr4:2565873
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.255+28703G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565873 | ||||||
| chr4:2565968
|
A | T | 1 | a0015c0015t0002g0028 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.255+28798A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2565968 | ||||||
| chr4:2566051
|
C | CTTTTTTT others(1): Show |
6 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0003g0317others(3): Show | 6 | HG02258.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.255+28888_255+2889 others(12): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2566051 | |||||
| chr4:2566079
|
G | A | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.255+28909G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2566079 | ||||||
| chr4:2566112
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.255+28942A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2566112 | ||||||
| chr4:2566121
|
G | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255+28951G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2566121 | ||||||
| chr4:2566133
|
T | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255+28963T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2566133 | ||||||
| chr4:2566138
|
T | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255+28968T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2566138 | ||||||
| chr4:2566140
|
T | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255+28970T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2566140 | ||||||
| chr4:2566205
|
G | A | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255+29035G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2566205 | ||||||
| chr4:2566260
|
C | G | 2 | a0004c0004t0001g0322a0007c0007t0001g0110 | 2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.255+29090C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2566260 | ||||||
| chr4:2566274
|
T | C | 1 | a0007c0007t0001g0110 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.255+29104T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2566274 | ||||||
| chr4:2566277
|
G | A | 75 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.255+29107G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2566277 | ||||||
| chr4:2566282
|
C | T | 1 | a0007c0007t0001g0110 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.255+29112C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2566282 | ||||||
| chr4:2566442
|
C | T | 3 | a0004c0004t0001g0318a0004c0004t0001g0322a0004c0017t0001g0324 | 3 | HG02258.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.255+29272C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2566442 | ||||||
| chr4:2566459
|
G | A | 1 | a0001c0002t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.255+29289G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2566459 | ||||||
| chr4:2566465
|
G | A | 6 | a0006c0008t0001g0121a0006c0008t0001g0125a0006c0008t0001g0126others(3): Show | 6 | HG02559.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+29295G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2566465 | ||||||
| chr4:2566620
|
C | T | 11 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0259others(8): Show | 11 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.255+29450C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2566620 | ||||||
| chr4:2566853
|
A | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-29231A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2566853 | ||||||
| chr4:2566916
|
T | C | 1 | a0001c0001t0002g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.256-29168T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2566916 | ||||||
| chr4:2566942
|
C | CT | 91 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(88): Show | 91 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.256-29127dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2566942 | |||||
| chr4:2567100
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.256-28984C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2567100 | ||||||
| chr4:2567106
|
A | AT | 29 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0002t0001g0001others(26): Show | 29 | HG00609.hp2 HG01243.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.256-28963dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2567106 | |||||
| chr4:2567106
|
AT | A | 6 | a0001c0001t0001g0146a0001c0001t0001g0202a0001c0001t0001g0204others(3): Show | 6 | NA18957.hp1 NA18989.hp1 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.256-28963delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2567106 | |||||
| chr4:2567194
|
C | T | 1 | a0004c0017t0001g0324 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.256-28890C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2567194 | ||||||
| chr4:2567228
|
G | GTGAGCCA others(12): Show |
2 | a0001c0001t0001g0133a0001c0001t0001g0200 | 2 | HG02132.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.256-28833_256-2881 others(23): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2567228 | |||||
| chr4:2567228
|
GTGAGCCA others(12): Show |
G | 12 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.256-28833_256-2881 others(23): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2567228 | |||||
| chr4:2567243
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.256-28841C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2567243 | ||||||
| chr4:2567352
|
T | C | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.256-28732T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2567352 | ||||||
| chr4:2567460
|
C | G | 1 | a0001c0001t0007g0129 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.256-28624C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2567460 | ||||||
| chr4:2567729
|
G | A | 31 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(28): Show | 31 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.256-28355G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2567729 | ||||||
| chr4:2567730
|
T | C | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.256-28354T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2567730 | ||||||
| chr4:2567785
|
T | C | 1 | a0001c0001t0002g0039 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.256-28299T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2567785 | ||||||
| chr4:2567819
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.256-28265G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2567819 | ||||||
| chr4:2568080
|
C | T | 1 | a0001c0001t0008g0249 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.256-28004C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2568080 | ||||||
| chr4:2568096
|
C | T | 1 | a0003c0003t0004g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.256-27988C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2568096 | ||||||
| chr4:2568198
|
T | C | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-27886T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2568198 | ||||||
| chr4:2568452
|
G | T | 323 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(320): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.256-27632G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2568452 | ||||||
| chr4:2568517
|
G | C | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.256-27567G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2568517 | ||||||
| chr4:2568684
|
A | G | 323 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(320): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.256-27400A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2568684 | ||||||
| chr4:2568902
|
CTT | C | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.256-27180_256-2717 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2568902 | |||||
| chr4:2568973
|
C | CT | 246 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0123others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.256-27090dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2568973 | |||||
| chr4:2568973
|
C | CTT | 14 | a0001c0001t0001g0184a0001c0001t0001g0200a0001c0001t0001g0225others(11): Show | 14 | HG00438.hp1 HG00544.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.256-27091_256-2709 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2568973 | |||||
| chr4:2568973
|
CT | C | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.256-27090delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2568973 | |||||
| chr4:2569110
|
C | G | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.256-26974C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2569110 | ||||||
| chr4:2569111
|
A | C | 1 | a0001c0001t0001g0133 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.256-26973A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2569111 | ||||||
| chr4:2569135
|
A | G | 83 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.256-26949A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2569135 | ||||||
| chr4:2569186
|
A | G | 322 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(319): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.256-26898A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2569186 | ||||||
| chr4:2569298
|
A | G | 1 | a0001c0001t0002g0048 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.256-26786A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2569298 | ||||||
| chr4:2569303
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-26781C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2569303 | ||||||
| chr4:2569308
|
G | A | 1 | a0003c0003t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.256-26776G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2569308 | ||||||
| chr4:2569400
|
C | T | 10 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0259others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.256-26684C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2569400 | ||||||
| chr4:2569419
|
C | T | 5 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0166others(2): Show | 5 | HG00639.hp1 HG01175.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.256-26665C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2569419 | ||||||
| chr4:2569542
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-26542G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2569542 | ||||||
| chr4:2569561
|
G | C | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.256-26523G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2569561 | ||||||
| chr4:2569600
|
C | G | 1 | a0001c0001t0001g0255 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.256-26484C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2569600 | ||||||
| chr4:2569757
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0003g0154 | 2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.256-26327G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2569757 | ||||||
| chr4:2569762
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.256-26322C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2569762 | ||||||
| chr4:2569915
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.256-26169T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2569915 | ||||||
| chr4:2569968
|
C | G | 1 | a0001c0001t0001g0306 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.256-26116C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2569968 | ||||||
| chr4:2569969
|
G | T | 103 | a0001c0001t0001g0065a0001c0001t0002g0006a0001c0001t0002g0007others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.256-26115G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2569969 | ||||||
| chr4:2570059
|
A | T | 74 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.256-26025A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2570059 | ||||||
| chr4:2570072
|
T | TGAGAGTA others(311): Show |
20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.256-25994_256-2599 others(322): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2570072 | |||||
| chr4:2570121
|
G | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.256-25963G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2570121 | ||||||
| chr4:2570219
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.256-25865G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2570219 | ||||||
| chr4:2570237
|
C | T | 3 | a0001c0001t0001g0261a0001c0001t0001g0265a0001c0001t0001g0289 | 3 | HG02165.hp1 NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.256-25847C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2570237 | ||||||
| chr4:2570270
|
G | T | 1 | a0001c0001t0001g0209 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.256-25814G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2570270 | ||||||
| chr4:2570438
|
A | G | 2 | a0006c0008t0001g0125a0006c0008t0001g0126 | 2 | HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.256-25646A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2570438 | ||||||
| chr4:2570552
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.256-25532C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2570552 | ||||||
| chr4:2570787
|
C | T | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.256-25297C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2570787 | ||||||
| chr4:2570873
|
C | G | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.256-25211C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2570873 | ||||||
| chr4:2570890
|
G | A | 7 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0032others(4): Show | 7 | HG00558.hp2 HG01074.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.256-25194G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2570890 | ||||||
| chr4:2570933
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.256-25151G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2570933 | ||||||
| chr4:2570937
|
A | T | 1 | a0001c0001t0001g0212 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.256-25147A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2570937 | ||||||
| chr4:2571196
|
G | A | 1 | a0005c0005t0004g0141 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.256-24888G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2571196 | ||||||
| chr4:2571232
|
G | A | 2 | a0001c0001t0001g0257a0001c0001t0001g0309 | 2 | NA18959.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.256-24852G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2571232 | ||||||
| chr4:2571274
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-24810C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2571274 | ||||||
| chr4:2571283
|
A | G | 31 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(28): Show | 31 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.256-24801A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2571283 | ||||||
| chr4:2571434
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.256-24650C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2571434 | ||||||
| chr4:2571558
|
T | G | 3 | a0001c0001t0001g0251a0001c0001t0001g0258a0001c0001t0001g0278 | 3 | HG01099.hp2 HG01106.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.256-24526T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2571558 | ||||||
| chr4:2571654
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.256-24430C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2571654 | ||||||
| chr4:2571767
|
C | T | 3 | a0001c0002t0003g0112a0001c0002t0003g0120a0001c0002t0013g0117 | 3 | HG01516.hp1 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.256-24317C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2571767 | ||||||
| chr4:2572092
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-23992G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2572092 | ||||||
| chr4:2572114
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-23970G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2572114 | ||||||
| chr4:2572143
|
C | T | 9 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(6): Show | 9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.256-23941C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2572143 | ||||||
| chr4:2572165
|
CA | C | 307 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(304): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.256-23901delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2572165 | |||||
| chr4:2572165
|
CAA | C | 10 | a0001c0001t0002g0329a0004c0004t0001g0321a0004c0004t0001g0322others(7): Show | 10 | HG02257.hp1 HG02615.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.256-23902_256-2390 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2572165 | |||||
| chr4:2572328
|
C | CA | 162 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(159): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.256-23740dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2572328 | |||||
| chr4:2572473
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-23611G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2572473 | ||||||
| chr4:2572524
|
G | T | 1 | a0001c0001t0001g0255 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.256-23560G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2572524 | ||||||
| chr4:2572691
|
G | A | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.256-23393G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2572691 | ||||||
| chr4:2572777
|
A | AT | 79 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(76): Show |
intron_variant | MODIFIER | c.256-23287dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2572777 | |||||
| chr4:2572777
|
AT | A | 22 | a0001c0001t0001g0133a0001c0001t0001g0144a0001c0001t0001g0157others(19): Show | 22 | HG00544.hp1 HG01070.hp2 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.256-23287delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2572777 | |||||
| chr4:2572798
|
A | T | 83 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.256-23286A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2572798 | ||||||
| chr4:2572800
|
A | G | 1 | a0001c0001t0002g0094 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.256-23284A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2572800 | ||||||
| chr4:2572833
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.256-23251G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2572833 | ||||||
| chr4:2572887
|
AGTGGCGA others(1): Show |
A | 11 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0259others(8): Show | 11 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-23195_256-2318 others(12): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2572887 | |||||
| chr4:2572939
|
C | A | 1 | a0001c0001t0001g0251 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.256-23145C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2572939 | ||||||
| chr4:2572972
|
T | C | 1 | a0001c0001t0004g0191 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.256-23112T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2572972 | ||||||
| chr4:2573270
|
T | C | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-22814T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2573270 | ||||||
| chr4:2573513
|
C | CA | 8 | a0001c0001t0001g0193a0001c0001t0002g0053a0004c0004t0001g0318others(5): Show | 8 | HG02257.hp1 HG02258.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.256-22555dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2573513 | |||||
| chr4:2573639
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-22445C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2573639 | ||||||
| chr4:2573658
|
G | A | 1 | a0003c0003t0011g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.256-22426G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2573658 | ||||||
| chr4:2573876
|
C | G | 3 | a0001c0002t0003g0112a0001c0002t0003g0120a0001c0002t0013g0117 | 3 | HG01516.hp1 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.256-22208C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2573876 | ||||||
| chr4:2573925
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-22159C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2573925 | ||||||
| chr4:2573932
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-22152G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2573932 | ||||||
| chr4:2573988
|
T | A | 1 | a0001c0001t0001g0289 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.256-22096T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2573988 | ||||||
| chr4:2574169
|
A | G | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.256-21915A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2574169 | ||||||
| chr4:2574221
|
CAT | C | 14 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(11): Show | 14 | HG01167.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.256-21862_256-2186 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2574221 | ||||||
| chr4:2574296
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-21788C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2574296 | ||||||
| chr4:2574326
|
C | G | 1 | a0001c0001t0001g0269 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.256-21758C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2574326 | ||||||
| chr4:2574375
|
G | A | 2 | a0001c0001t0001g0133a0005c0005t0004g0134 | 2 | HG00408.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.256-21709G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2574375 | ||||||
| chr4:2574506
|
T | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-21578T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2574506 | ||||||
| chr4:2574607
|
C | T | 2 | a0004c0004t0001g0318a0004c0004t0001g0322 | 2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.256-21477C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2574607 | ||||||
| chr4:2574613
|
A | G | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.256-21471A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2574613 | ||||||
| chr4:2574664
|
T | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-21420T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2574664 | ||||||
| chr4:2574768
|
C | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-21316C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2574768 | ||||||
| chr4:2574862
|
G | C | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.256-21222G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2574862 | ||||||
| chr4:2574887
|
T | C | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.256-21197T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2574887 | ||||||
| chr4:2574934
|
G | A | 1 | a0001c0001t0001g0251 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.256-21150G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2574934 | ||||||
| chr4:2575036
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.256-21048G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2575036 | ||||||
| chr4:2575041
|
A | C | 2 | a0001c0021t0003g0143a0014c0024t0018g0139 | 2 | HG01884.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.256-21043A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2575041 | ||||||
| chr4:2575223
|
C | T | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.256-20861C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2575223 | ||||||
| chr4:2575272
|
T | C | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.256-20812T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2575272 | ||||||
| chr4:2575465
|
A | AT | 31 | a0001c0001t0001g0169a0001c0001t0001g0212a0001c0001t0001g0217others(28): Show | 31 | HG00438.hp2 HG00609.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.256-20600dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2575465 | |||||
| chr4:2575465
|
A | ATT | 16 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0001t0002g0010others(13): Show | 16 | HG00408.hp1 HG01074.hp1 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.256-20601_256-2060 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2575465 | |||||
| chr4:2575465
|
AT | A | 76 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.256-20600delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2575465 | |||||
| chr4:2575627
|
T | C | 1 | a0001c0001t0002g0085 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.256-20457T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2575627 | ||||||
| chr4:2575655
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-20429C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2575655 | ||||||
| chr4:2575743
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-20341G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2575743 | ||||||
| chr4:2575761
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-20323C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2575761 | ||||||
| chr4:2575875
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.256-20209C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2575875 | ||||||
| chr4:2576042
|
A | G | 9 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(6): Show | 9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.256-20042A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2576042 | ||||||
| chr4:2576089
|
G | GTTAT | 12 | a0001c0001t0001g0122a0001c0001t0001g0133a0002c0012t0004g0328others(9): Show | 12 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.256-19976_256-1997 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2576089 | |||||
| chr4:2576270
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.256-19814T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2576270 | ||||||
| chr4:2576289
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.256-19795G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2576289 | ||||||
| chr4:2576313
|
T | G | 3 | a0001c0001t0001g0261a0001c0001t0001g0265a0001c0001t0001g0289 | 3 | HG02165.hp1 NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.256-19771T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2576313 | ||||||
| chr4:2576367
|
G | A | 1 | a0005c0005t0002g0138 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.256-19717G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2576367 | ||||||
| chr4:2576549
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.256-19535G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2576549 | ||||||
| chr4:2576571
|
C | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-19513C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2576571 | ||||||
| chr4:2576870
|
A | G | 4 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0008g0215others(1): Show | 4 | HG01884.hp1 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.256-19214A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2576870 | ||||||
| chr4:2576924
|
A | G | 101 | a0001c0001t0001g0065a0001c0001t0001g0273a0001c0001t0002g0006others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.256-19160A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2576924 | ||||||
| chr4:2576928
|
A | G | 1 | a0001c0001t0002g0034 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.256-19156A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2576928 | ||||||
| chr4:2577126
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.256-18958A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2577126 | ||||||
| chr4:2577175
|
CGAA | C | 200 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0123others(197): Show | 200 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.256-18907_256-1890 others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2577175 | |||||
| chr4:2577183
|
C | T | 3 | a0004c0004t0001g0318a0004c0004t0001g0322a0004c0017t0001g0324 | 3 | HG02258.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.256-18901C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2577183 | ||||||
| chr4:2577373
|
T | G | 1 | a0001c0001t0002g0097 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.256-18711T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2577373 | ||||||
| chr4:2577411
|
G | GTTTTTTT others(7): Show |
1 | a0001c0001t0001g0264 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.256-18663_256-1866 others(18): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2577411 | |||||
| chr4:2577411
|
G | GTTTTTTT others(5): Show |
2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | HG02004.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.256-18663_256-1866 others(16): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2577411 | |||||
| chr4:2577411
|
G | GTTTTTTT others(7): Show |
1 | a0001c0001t0002g0048 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.256-18663_256-1866 others(18): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2577411 | |||||
| chr4:2577411
|
GT | G | 13 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0021t0003g0143others(10): Show | 13 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.256-18663delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2577411 | |||||
| chr4:2577417
|
TTTTTG | T | 8 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(5): Show | 8 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.256-18662_256-1865 others(9): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2577417 | |||||
| chr4:2577422
|
G | GT | 47 | a0001c0001t0001g0158a0001c0001t0001g0173a0001c0001t0001g0177others(44): Show | 47 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.256-18648dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2577422 | |||||
| chr4:2577422
|
G | GTTTTTTT others(5): Show |
40 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(37): Show | 40 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.256-18659_256-1864 others(16): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2577422 | |||||
| chr4:2577422
|
G | GTTTTTTT others(6): Show |
27 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0001g0255others(24): Show | 27 | HG00673.hp1 HG01099.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.256-18660_256-1864 others(17): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2577422 | |||||
| chr4:2577422
|
G | GTTTTTTT others(7): Show |
4 | a0001c0001t0001g0256a0001c0001t0001g0279a0001c0001t0001g0285others(1): Show | 4 | HG02109.hp2 HG03492.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.256-18661_256-1864 others(18): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2577422 | |||||
| chr4:2577422
|
G | T | 8 | a0001c0001t0001g0264a0001c0001t0001g0304a0001c0001t0001g0305others(5): Show | 8 | HG01071.hp2 HG01168.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.256-18662G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2577422 | ||||||
| chr4:2577521
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.256-18563C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2577521 | ||||||
| chr4:2577697
|
G | C | 2 | a0001c0001t0001g0255a0002c0006t0001g0242 | 2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.256-18387G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2577697 | ||||||
| chr4:2577782
|
T | C | 2 | a0004c0004t0001g0323a0004c0004t0001g0327 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.256-18302T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2577782 | ||||||
| chr4:2578045
|
C | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-18039C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2578045 | ||||||
| chr4:2578150
|
T | C | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.256-17934T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2578150 | ||||||
| chr4:2578169
|
A | G | 2 | a0001c0001t0001g0277a0001c0001t0001g0281 | 2 | NA18957.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.256-17915A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2578169 | ||||||
| chr4:2578284
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.256-17800C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2578284 | ||||||
| chr4:2578444
|
T | G | 227 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0123others(224): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.256-17640T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2578444 | ||||||
| chr4:2578445
|
G | C | 1 | a0007c0007t0001g0115 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.256-17639G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2578445 | ||||||
| chr4:2578610
|
C | T | 97 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(94): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.256-17474C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2578610 | ||||||
| chr4:2578654
|
A | G | 3 | a0001c0001t0001g0262a0001c0001t0001g0285a0001c0016t0001g0308 | 3 | HG02109.hp2 HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.256-17430A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2578654 | ||||||
| chr4:2578656
|
C | G | 1 | a0001c0001t0001g0254 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.256-17428C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2578656 | ||||||
| chr4:2578741
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.256-17343A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2578741 | ||||||
| chr4:2578819
|
A | G | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.256-17265A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2578819 | ||||||
| chr4:2578869
|
A | AGAG | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-17195_256-1719 others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2578869 | |||||
| chr4:2578889
|
A | C | 91 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(88): Show | 91 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.256-17195A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2578889 | ||||||
| chr4:2578892
|
C | T | 4 | a0001c0001t0002g0011a0001c0001t0002g0040a0001c0001t0002g0047others(1): Show | 4 | NA18967.hp1 NA18970.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.256-17192C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2578892 | ||||||
| chr4:2578907
|
T | C | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.256-17177T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2578907 | ||||||
| chr4:2578921
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-17163C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2578921 | ||||||
| chr4:2578996
|
C | T | 1 | a0002c0012t0004g0328 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.256-17088C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2578996 | ||||||
| chr4:2579099
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.256-16985A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2579099 | ||||||
| chr4:2579173
|
G | A | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.256-16911G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2579173 | ||||||
| chr4:2579175
|
TTTAAA | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-16904_256-1690 others(9): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2579175 | |||||
| chr4:2579221
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.256-16863G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2579221 | ||||||
| chr4:2579232
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.256-16852C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2579232 | ||||||
| chr4:2579311
|
A | G | 1 | a0001c0002t0003g0112 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.256-16773A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2579311 | ||||||
| chr4:2579328
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.256-16756C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2579328 | ||||||
| chr4:2579351
|
T | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-16733T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2579351 | ||||||
| chr4:2579358
|
G | A | 5 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(2): Show | 5 | HG01891.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.256-16726G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2579358 | ||||||
| chr4:2579369
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.256-16715C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2579369 | ||||||
| chr4:2579686
|
G | A | 1 | a0001c0002t0013g0117 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.256-16398G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2579686 | ||||||
| chr4:2579718
|
A | C | 4 | a0001c0001t0001g0257a0001c0001t0001g0292a0001c0001t0001g0309others(1): Show | 4 | NA18940.hp1 NA18959.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.256-16366A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2579718 | ||||||
| chr4:2579723
|
GAAA | G | 91 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(88): Show | 91 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.256-16359_256-1635 others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2579723 | |||||
| chr4:2579814
|
T | C | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.256-16270T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2579814 | ||||||
| chr4:2580037
|
A | G | 1 | a0001c0001t0002g0098 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.256-16047A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580037 | ||||||
| chr4:2580136
|
A | G | 77 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.256-15948A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580136 | ||||||
| chr4:2580267
|
T | G | 1 | a0001c0001t0002g0053 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.256-15817T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580267 | ||||||
| chr4:2580378
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0185 | 2 | HG01081.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.256-15706G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580378 | ||||||
| chr4:2580412
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.256-15672C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580412 | ||||||
| chr4:2580425
|
G | C | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-15659G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580425 | ||||||
| chr4:2580506
|
A | C | 1 | a0001c0001t0002g0032 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.256-15578A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580506 | ||||||
| chr4:2580747
|
T | C | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-15337T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580747 | ||||||
| chr4:2580787
|
G | A | 11 | a0001c0001t0001g0122a0001c0001t0001g0133a0002c0012t0004g0328others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-15297G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580787 | ||||||
| chr4:2580830
|
A | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-15254A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580830 | ||||||
| chr4:2580835
|
T | A | 75 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.256-15249T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580835 | ||||||
| chr4:2580895
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.256-15189C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580895 | ||||||
| chr4:2580899
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.256-15185G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580899 | ||||||
| chr4:2580901
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.256-15183G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580901 | ||||||
| chr4:2580903
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.256-15181G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580903 | ||||||
| chr4:2580905
|
A | G | 3 | a0001c0001t0001g0303a0009c0010t0014g0228a0009c0010t0015g0229 | 3 | HG01070.hp1 HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-15179A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580905 | ||||||
| chr4:2580908
|
T | A | 1 | a0001c0001t0001g0303 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.256-15176T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580908 | ||||||
| chr4:2580912
|
A | G | 1 | a0001c0001t0001g0303 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.256-15172A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580912 | ||||||
| chr4:2580924
|
T | A | 1 | a0001c0001t0001g0303 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.256-15160T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580924 | ||||||
| chr4:2580926
|
T | G | 1 | a0001c0001t0001g0303 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.256-15158T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580926 | ||||||
| chr4:2580957
|
G | A | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.256-15127G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580957 | ||||||
| chr4:2580985
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.256-15099C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580985 | ||||||
| chr4:2580988
|
G | C | 93 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(90): Show | 93 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.256-15096G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2580988 | ||||||
| chr4:2581123
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-14961C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2581123 | ||||||
| chr4:2581132
|
A | AAAC | 125 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.256-14943_256-1494 others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2581132 | |||||
| chr4:2581144
|
A | C | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.256-14940A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2581144 | ||||||
| chr4:2581211
|
G | GT | 77 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.256-14871dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2581211 | |||||
| chr4:2581255
|
C | CT | 77 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.256-14814dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2581255 | |||||
| chr4:2581255
|
CT | C | 24 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(21): Show | 24 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.256-14814delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2581255 | |||||
| chr4:2581324
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.256-14760G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2581324 | ||||||
| chr4:2581325
|
C | A | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.256-14759C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2581325 | ||||||
| chr4:2581537
|
A | G | 77 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.256-14547A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2581537 | ||||||
| chr4:2581668
|
C | T | 9 | a0001c0001t0001g0122a0002c0012t0004g0328a0005c0005t0004g0128others(6): Show | 9 | HG01074.hp1 HG01975.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.256-14416C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2581668 | ||||||
| chr4:2581669
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-14415G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2581669 | ||||||
| chr4:2581676
|
C | T | 79 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.256-14408C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2581676 | ||||||
| chr4:2581697
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.256-14387G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2581697 | ||||||
| chr4:2581710
|
G | A | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.256-14374G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2581710 | ||||||
| chr4:2581813
|
A | C | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.256-14271A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2581813 | ||||||
| chr4:2581819
|
A | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0166 | 2 | HG01175.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.256-14265A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2581819 | ||||||
| chr4:2581851
|
C | T | 6 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(3): Show | 6 | HG01884.hp1 HG01891.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.256-14233C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2581851 | ||||||
| chr4:2581891
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.256-14193G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2581891 | ||||||
| chr4:2582360
|
T | C | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-13724T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2582360 | ||||||
| chr4:2582481
|
T | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.256-13603T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2582481 | ||||||
| chr4:2582591
|
TTTG | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-13484_256-1348 others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2582591 | |||||
| chr4:2582615
|
C | T | 1 | a0003c0003t0004g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.256-13469C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2582615 | ||||||
| chr4:2582670
|
A | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-13414A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2582670 | ||||||
| chr4:2582780
|
T | C | 1 | a0001c0001t0007g0137 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.256-13304T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2582780 | ||||||
| chr4:2582842
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.256-13242G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2582842 | ||||||
| chr4:2582924
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-13160C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2582924 | ||||||
| chr4:2582989
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.256-13095A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2582989 | ||||||
| chr4:2582990
|
C | T | 76 | a0001c0001t0001g0226a0001c0001t0001g0241a0001c0001t0001g0244others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.256-13094C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2582990 | ||||||
| chr4:2583007
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.256-13077C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2583007 | ||||||
| chr4:2583072
|
G | A | 12 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0021t0003g0143others(9): Show | 12 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.256-13012G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2583072 | ||||||
| chr4:2583135
|
G | A | 6 | a0001c0001t0001g0252a0001c0001t0001g0271a0001c0001t0001g0272others(3): Show | 6 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(3): Show |
intron_variant | MODIFIER | c.256-12949G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2583135 | ||||||
| chr4:2583390
|
G | T | 1 | a0001c0001t0001g0307 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.256-12694G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2583390 | ||||||
| chr4:2583540
|
G | C | 11 | a0001c0001t0001g0122a0001c0001t0001g0133a0002c0012t0004g0328others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-12544G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2583540 | ||||||
| chr4:2583649
|
T | C | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-12435T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2583649 | ||||||
| chr4:2583669
|
A | G | 1 | a0007c0007t0001g0110 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.256-12415A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2583669 | ||||||
| chr4:2584126
|
A | T | 4 | a0001c0001t0001g0257a0001c0001t0001g0292a0001c0001t0001g0309others(1): Show | 4 | NA18940.hp1 NA18959.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.256-11958A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2584126 | ||||||
| chr4:2584168
|
T | C | 1 | a0001c0001t0002g0054 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.256-11916T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2584168 | ||||||
| chr4:2584328
|
A | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-11756A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2584328 | ||||||
| chr4:2584425
|
C | CA | 11 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0002g0063others(8): Show | 11 | HG00735.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.256-11643dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2584425 | |||||
| chr4:2584453
|
A | G | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.256-11631A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2584453 | ||||||
| chr4:2584519
|
A | C | 4 | a0001c0001t0001g0257a0001c0001t0001g0292a0001c0001t0001g0309others(1): Show | 4 | NA18940.hp1 NA18959.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.256-11565A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2584519 | ||||||
| chr4:2584525
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.256-11559C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2584525 | ||||||
| chr4:2584692
|
C | T | 2 | a0001c0001t0002g0054a0001c0001t0002g0071 | 2 | NA18974.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.256-11392C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2584692 | ||||||
| chr4:2584824
|
C | T | 1 | a0001c0002t0009g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.256-11260C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2584824 | ||||||
| chr4:2584877
|
A | G | 28 | a0001c0001t0001g0123a0001c0001t0001g0142a0001c0001t0001g0144others(25): Show | 28 | HG00438.hp1 HG00639.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.256-11207A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2584877 | ||||||
| chr4:2584880
|
G | A | 1 | a0001c0002t0001g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.256-11204G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2584880 | ||||||
| chr4:2584902
|
C | A | 1 | a0002c0011t0003g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.256-11182C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2584902 | ||||||
| chr4:2585113
|
A | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-10971A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2585113 | ||||||
| chr4:2585293
|
T | C | 12 | a0001c0001t0001g0122a0001c0001t0001g0133a0002c0012t0004g0328others(9): Show | 12 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.256-10791T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2585293 | ||||||
| chr4:2585554
|
A | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-10530A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2585554 | ||||||
| chr4:2585748
|
A | G | 229 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0123others(226): Show | 229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.256-10336A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2585748 | ||||||
| chr4:2585763
|
C | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0309a0001c0001t0001g0311 | 3 | NA18940.hp1 NA18959.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.256-10321C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2585763 | ||||||
| chr4:2585796
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.256-10288C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2585796 | ||||||
| chr4:2585837
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.256-10247G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2585837 | ||||||
| chr4:2585916
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.256-10168G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2585916 | ||||||
| chr4:2586090
|
A | C | 92 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(89): Show | 92 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.256-9994A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2586090 | ||||||
| chr4:2586104
|
G | A | 2 | a0001c0021t0003g0143a0014c0024t0018g0139 | 2 | HG01884.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.256-9980G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2586104 | ||||||
| chr4:2586197
|
G | C | 227 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0123others(224): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.256-9887G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2586197 | ||||||
| chr4:2586244
|
C | CA | 66 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(63): Show | 66 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.256-9829dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2586244 | |||||
| chr4:2586244
|
CA | C | 13 | a0001c0001t0001g0276a0003c0003t0001g0236a0004c0004t0001g0318others(10): Show | 13 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.256-9829delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2586244 | |||||
| chr4:2586252
|
A | T | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.256-9832A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2586252 | ||||||
| chr4:2586254
|
A | AT | 8 | a0001c0001t0001g0219a0001c0001t0007g0129a0001c0001t0007g0137others(5): Show | 8 | HG01167.hp2 HG02257.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.256-9830_256-9829i others(3): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2586254 | ||||||
| chr4:2586254
|
A | T | 105 | a0001c0001t0001g0176a0001c0001t0001g0223a0001c0001t0001g0225others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.256-9830A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2586254 | ||||||
| chr4:2586255
|
AT | A | 4 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(1): Show | 4 | HG01891.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.256-9828delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2586255 | ||||||
| chr4:2586256
|
T | A | 21 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0001t0001g0166others(18): Show | 21 | HG00558.hp2 HG00609.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.256-9828T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2586256 | ||||||
| chr4:2586336
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-9748C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2586336 | ||||||
| chr4:2586437
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.256-9647T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2586437 | ||||||
| chr4:2586574
|
G | A | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.256-9510G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2586574 | ||||||
| chr4:2586654
|
T | C | 5 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(2): Show | 5 | HG00673.hp1 HG02015.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.256-9430T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2586654 | ||||||
| chr4:2586694
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.256-9390C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2586694 | ||||||
| chr4:2586763
|
C | G | 1 | a0001c0001t0001g0147 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.256-9321C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2586763 | ||||||
| chr4:2586848
|
C | T | 3 | a0001c0001t0001g0151a0001c0001t0001g0166a0001c0001t0001g0167 | 3 | HG01175.hp1 HG01358.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.256-9236C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2586848 | ||||||
| chr4:2587091
|
A | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-8993A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2587091 | ||||||
| chr4:2587193
|
A | G | 2 | a0001c0001t0001g0267a0001c0001t0001g0293 | 2 | NA18946.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.256-8891A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2587193 | ||||||
| chr4:2587222
|
T | G | 56 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(53): Show | 56 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.256-8862T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2587222 | ||||||
| chr4:2587297
|
C | T | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.256-8787C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2587297 | ||||||
| chr4:2587429
|
G | A | 1 | a0006c0008t0001g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.256-8655G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2587429 | ||||||
| chr4:2587513
|
A | G | 20 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(17): Show | 20 | HG00609.hp2 HG02145.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.256-8571A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2587513 | ||||||
| chr4:2587561
|
G | T | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.256-8523G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2587561 | ||||||
| chr4:2587566
|
C | CCT | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.256-8517_256-8516d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2587566 | |||||
| chr4:2587649
|
G | A | 11 | a0001c0001t0001g0122a0001c0001t0001g0133a0002c0012t0004g0328others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-8435G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2587649 | ||||||
| chr4:2587687
|
G | T | 1 | a0003c0003t0005g0164 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.256-8397G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2587687 | ||||||
| chr4:2587915
|
G | A | 2 | a0001c0001t0001g0284a0001c0001t0001g0291 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.256-8169G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2587915 | ||||||
| chr4:2588064
|
G | C | 1 | a0001c0001t0001g0280 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.256-8020G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2588064 | ||||||
| chr4:2588220
|
C | G | 1 | a0001c0001t0001g0245 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.256-7864C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2588220 | ||||||
| chr4:2588431
|
G | T | 1 | a0001c0001t0001g0245 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.256-7653G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2588431 | ||||||
| chr4:2588496
|
G | A | 1 | a0001c0001t0002g0329 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.256-7588G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2588496 | ||||||
| chr4:2588533
|
G | T | 3 | a0001c0001t0001g0263a0001c0001t0001g0290a0002c0006t0001g0287 | 3 | HG00741.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.256-7551G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2588533 | ||||||
| chr4:2588597
|
A | G | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0329 | 3 | HG01106.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.256-7487A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2588597 | ||||||
| chr4:2588698
|
A | AT | 14 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(11): Show | 14 | HG01167.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.256-7383dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2588698 | |||||
| chr4:2588821
|
A | G | 2 | a0001c0001t0001g0251a0001c0001t0001g0258 | 2 | HG01106.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.256-7263A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2588821 | ||||||
| chr4:2589439
|
C | T | 1 | a0001c0001t0002g0104 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.256-6645C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2589439 | ||||||
| chr4:2589472
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.256-6612G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2589472 | ||||||
| chr4:2589638
|
T | A | 1 | a0001c0001t0001g0163 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.256-6446T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2589638 | ||||||
| chr4:2589902
|
C | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-6182C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2589902 | ||||||
| chr4:2589991
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.256-6093C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2589991 | ||||||
| chr4:2590004
|
G | T | 1 | a0001c0001t0001g0275 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.256-6080G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590004 | ||||||
| chr4:2590121
|
C | T | 6 | a0006c0008t0001g0121a0006c0008t0001g0125a0006c0008t0001g0126others(3): Show | 6 | HG02559.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.256-5963C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590121 | ||||||
| chr4:2590134
|
C | CA | 71 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0245others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.256-5935dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590134 | |||||
| chr4:2590134
|
CA | C | 38 | a0001c0001t0001g0168a0001c0001t0001g0225a0001c0001t0002g0022others(35): Show | 38 | HG01167.hp2 HG01243.hp2 HG01516.hp1 others(35): Show |
intron_variant | MODIFIER | c.256-5935delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590134 | |||||
| chr4:2590146
|
A | G | 6 | a0006c0008t0001g0121a0006c0008t0001g0125a0006c0008t0001g0126others(3): Show | 6 | HG02559.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.256-5938A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590146 | ||||||
| chr4:2590147
|
AAAG | A | 6 | a0001c0001t0001g0248a0001c0001t0001g0255a0001c0001t0001g0259others(3): Show | 6 | HG02055.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.256-5934_256-5932d others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590147 | |||||
| chr4:2590150
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-5934G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590150 | ||||||
| chr4:2590313
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.256-5771C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590313 | ||||||
| chr4:2590385
|
A | C | 11 | a0001c0001t0001g0122a0001c0001t0001g0133a0002c0012t0004g0328others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-5699A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590385 | ||||||
| chr4:2590390
|
G | A | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.256-5694G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590390 | ||||||
| chr4:2590438
|
CT | C | 75 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.256-5645delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590438 | ||||||
| chr4:2590450
|
C | T | 1 | a0003c0003t0011g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.256-5634C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590450 | ||||||
| chr4:2590463
|
C | CA | 23 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(20): Show | 23 | HG00735.hp2 HG01516.hp2 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.256-5609dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590463 | |||||
| chr4:2590465
|
AAAAAAAA others(4): Show |
A | 9 | a0001c0001t0001g0133a0002c0012t0004g0328a0005c0005t0004g0128others(6): Show | 9 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.256-5609_256-5599d others(13): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590465 | |||||
| chr4:2590466
|
AAAAAAAA others(3): Show |
A | 9 | a0001c0001t0002g0021a0001c0001t0002g0027a0001c0001t0002g0040others(6): Show | 9 | HG00738.hp1 HG00741.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.256-5578_256-5569d others(12): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590466 | |||||
| chr4:2590469
|
AAAAAAAC others(30): Show |
A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-5608_256-5572d others(39): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590469 | |||||
| chr4:2590471
|
AAAAACAA others(18): Show |
A | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.256-5608_256-5584d others(27): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590471 | |||||
| chr4:2590471
|
AAAAACAA others(28): Show |
A | 6 | a0001c0016t0001g0308a0004c0004t0001g0322a0004c0004t0001g0323others(3): Show | 6 | HG02145.hp1 HG02257.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.256-5608_256-5574d others(37): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590471 | |||||
| chr4:2590472
|
AAAACAAA others(7): Show |
A | 1 | a0006c0008t0001g0216 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.256-5608_256-5595d others(16): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590472 | |||||
| chr4:2590472
|
AAAACAAA others(27): Show |
A | 1 | a0004c0004t0001g0318 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.256-5608_256-5575d others(36): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590472 | |||||
| chr4:2590474
|
AACAAAAA others(5): Show |
A | 2 | a0005c0005t0004g0141a0006c0008t0001g0132 | 2 | NA18984.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.256-5608_256-5597d others(14): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590474 | |||||
| chr4:2590474
|
AACAAAAA others(15): Show |
A | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.256-5608_256-5587d others(24): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590474 | |||||
| chr4:2590475
|
AC | A | 28 | a0001c0001t0001g0152a0001c0001t0001g0202a0001c0001t0001g0207others(25): Show | 28 | HG00558.hp1 HG01167.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.256-5608delC | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590475 | ||||||
| chr4:2590475
|
ACAAAAAA others(24): Show |
A | 1 | a0001c0002t0003g0116 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.256-5608_256-5578d others(33): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590475 | ||||||
| chr4:2590476
|
C | A | 142 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(139): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.256-5608C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590476 | ||||||
| chr4:2590478
|
A | C | 3 | a0001c0001t0001g0223a0001c0001t0001g0226a0001c0025t0001g0224 | 3 | HG02451.hp2 HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.256-5606A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590478 | ||||||
| chr4:2590480
|
A | C | 8 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(5): Show | 8 | HG02258.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.256-5604A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590480 | ||||||
| chr4:2590481
|
A | C | 1 | a0001c0001t0001g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.256-5603A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590481 | ||||||
| chr4:2590482
|
A | C | 7 | a0001c0001t0001g0151a0001c0001t0001g0166a0001c0001t0001g0223others(4): Show | 7 | HG01175.hp1 HG01358.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.256-5602A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590482 | ||||||
| chr4:2590484
|
A | C | 15 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0001g0156others(12): Show | 15 | HG00639.hp1 HG01361.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.256-5600A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590484 | ||||||
| chr4:2590485
|
A | C | 1 | a0001c0001t0003g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.256-5599A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590485 | ||||||
| chr4:2590486
|
C | A | 74 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(71): Show | 74 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.256-5598C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590486 | ||||||
| chr4:2590486
|
C | CA | 5 | a0001c0001t0002g0032a0001c0001t0002g0057a0001c0001t0002g0062others(2): Show | 5 | HG01109.hp1 HG01358.hp2 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.256-5589dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590486 | |||||
| chr4:2590486
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.256-5589_256-5579d others(13): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590486 | |||||
| chr4:2590486
|
CAAAAAAA others(19): Show |
C | 3 | a0006c0008t0001g0125a0006c0008t0001g0126a0006c0008t0001g0127 | 3 | HG02559.hp2 HG02818.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.256-5593_256-5568d others(28): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590486 | |||||
| chr4:2590487
|
A | C | 1 | a0005c0005t0004g0141 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.256-5597A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590487 | ||||||
| chr4:2590488
|
A | AC | 9 | a0001c0001t0001g0144a0001c0001t0001g0158a0001c0001t0001g0193others(6): Show | 9 | HG00642.hp1 NA18940.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.256-5596_256-5595i others(3): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590488 | ||||||
| chr4:2590488
|
A | C | 60 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(57): Show | 60 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.256-5596A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590488 | ||||||
| chr4:2590490
|
A | C | 10 | a0001c0001t0001g0202a0001c0001t0001g0219a0001c0001t0003g0154others(7): Show | 10 | HG01167.hp2 HG02257.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.256-5594A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590490 | ||||||
| chr4:2590490
|
AAAAAACA others(30): Show |
A | 11 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-5593_256-5557d others(39): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590490 | ||||||
| chr4:2590491
|
A | G | 5 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(2): Show | 5 | HG00673.hp1 HG02015.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.256-5593A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590491 | ||||||
| chr4:2590492
|
A | C | 78 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(75): Show | 78 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.256-5592A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590492 | ||||||
| chr4:2590494
|
A | C | 10 | a0001c0001t0001g0202a0001c0001t0001g0219a0001c0001t0003g0154others(7): Show | 10 | HG01167.hp2 HG02257.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.256-5590A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590494 | ||||||
| chr4:2590494
|
AAC | A | 9 | a0001c0001t0001g0133a0002c0012t0004g0328a0005c0005t0004g0128others(6): Show | 9 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.256-5588_256-5587d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590494 | |||||
| chr4:2590495
|
A | C | 1 | a0001c0001t0002g0009 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.256-5589A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590495 | ||||||
| chr4:2590496
|
C | A | 13 | a0001c0001t0001g0202a0001c0001t0001g0219a0001c0001t0003g0154others(10): Show | 13 | HG01167.hp2 HG02257.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.256-5588C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590496 | ||||||
| chr4:2590497
|
A | C | 10 | a0001c0001t0001g0122a0001c0001t0001g0133a0002c0012t0004g0328others(7): Show | 10 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.256-5587A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590497 | ||||||
| chr4:2590498
|
A | C | 10 | a0001c0001t0001g0202a0001c0001t0001g0219a0001c0001t0003g0154others(7): Show | 10 | HG01167.hp2 HG02257.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.256-5586A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590498 | ||||||
| chr4:2590500
|
A | C | 155 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(152): Show | 155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.256-5584A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590500 | ||||||
| chr4:2590501
|
A | C | 74 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.256-5583A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590501 | ||||||
| chr4:2590502
|
A | C | 11 | a0001c0001t0001g0167a0001c0001t0001g0202a0001c0001t0001g0219others(8): Show | 11 | HG01167.hp2 HG02257.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.256-5582A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590502 | ||||||
| chr4:2590504
|
A | C | 79 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(76): Show | 79 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.256-5580A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590504 | ||||||
| chr4:2590505
|
AC | A | 79 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(76): Show | 79 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.256-5578delC | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590505 | ||||||
| chr4:2590506
|
C | A | 76 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.256-5578C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590506 | ||||||
| chr4:2590506
|
C | CA | 12 | a0001c0001t0001g0167a0001c0001t0001g0202a0001c0001t0002g0025others(9): Show | 12 | HG00735.hp1 HG01167.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.256-5568dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590506 | |||||
| chr4:2590510
|
A | C | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.256-5574A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590510 | ||||||
| chr4:2590511
|
A | C | 1 | a0001c0002t0003g0116 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.256-5573A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590511 | ||||||
| chr4:2590512
|
A | C | 13 | a0001c0001t0001g0122a0001c0001t0001g0133a0002c0012t0004g0328others(10): Show | 13 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.256-5572A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590512 | ||||||
| chr4:2590512
|
AAAAAC | A | 20 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(17): Show | 20 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.256-5562_256-5558d others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590512 | |||||
| chr4:2590517
|
C | A | 20 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0001t0001g0305others(17): Show | 20 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.256-5567C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590517 | ||||||
| chr4:2590523
|
A | C | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.256-5561A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590523 | ||||||
| chr4:2590526
|
AT | A | 7 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0322others(4): Show | 7 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.256-5556delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590526 | |||||
| chr4:2590697
|
A | G | 1 | a0001c0001t0001g0275 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.256-5387A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590697 | ||||||
| chr4:2590809
|
C | T | 1 | a0001c0001t0002g0032 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.256-5275C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590809 | ||||||
| chr4:2590857
|
C | CTCTA | 6 | a0006c0008t0001g0121a0006c0008t0001g0125a0006c0008t0001g0126others(3): Show | 6 | HG02559.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.256-5226_256-5223d others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2590857 | |||||
| chr4:2590859
|
C | G | 3 | a0001c0001t0001g0152a0001c0001t0001g0231a0001c0001t0001g0232 | 3 | HG02647.hp1 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.256-5225C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590859 | ||||||
| chr4:2590895
|
C | T | 3 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0322 | 3 | HG02258.hp2 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.256-5189C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590895 | ||||||
| chr4:2590908
|
T | C | 18 | a0001c0016t0001g0308a0003c0003t0001g0233a0003c0003t0001g0234others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.256-5176T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590908 | ||||||
| chr4:2590981
|
C | A | 2 | a0001c0001t0002g0073a0001c0001t0002g0079 | 2 | NA18951.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.256-5103C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2590981 | ||||||
| chr4:2591026
|
C | CA | 21 | a0001c0001t0001g0122a0001c0001t0001g0133a0002c0012t0004g0328others(18): Show | 21 | HG00408.hp1 HG00609.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.256-5045dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2591026 | |||||
| chr4:2591069
|
A | G | 1 | a0001c0001t0002g0034 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.256-5015A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2591069 | ||||||
| chr4:2591180
|
A | C | 2 | a0001c0001t0001g0251a0001c0001t0001g0258 | 2 | HG01106.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.256-4904A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2591180 | ||||||
| chr4:2591287
|
T | A | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.256-4797T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2591287 | ||||||
| chr4:2591416
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.256-4668C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2591416 | ||||||
| chr4:2591540
|
A | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.256-4544A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2591540 | ||||||
| chr4:2591593
|
A | G | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.256-4491A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2591593 | ||||||
| chr4:2591726
|
C | G | 1 | a0001c0001t0008g0249 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.256-4358C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2591726 | ||||||
| chr4:2591848
|
G | T | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.256-4236G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2591848 | ||||||
| chr4:2592091
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.256-3993T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2592091 | ||||||
| chr4:2592161
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.256-3923C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2592161 | ||||||
| chr4:2592441
|
A | G | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.256-3643A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2592441 | ||||||
| chr4:2592467
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.256-3617A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2592467 | ||||||
| chr4:2592551
|
G | A | 2 | a0004c0004t0001g0323a0004c0004t0001g0327 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.256-3533G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2592551 | ||||||
| chr4:2592581
|
C | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.256-3503C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2592581 | ||||||
| chr4:2592581
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.256-3503C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2592581 | ||||||
| chr4:2593009
|
C | T | 1 | a0001c0002t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.256-3075C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2593009 | ||||||
| chr4:2593202
|
A | G | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.256-2882A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2593202 | ||||||
| chr4:2593251
|
A | G | 66 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(63): Show | 66 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.256-2833A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2593251 | ||||||
| chr4:2593447
|
T | G | 1 | a0006c0008t0001g0005 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.256-2637T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2593447 | ||||||
| chr4:2593602
|
C | G | 1 | a0001c0001t0001g0209 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.256-2482C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2593602 | ||||||
| chr4:2593698
|
T | C | 1 | a0003c0003t0004g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.256-2386T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2593698 | ||||||
| chr4:2593708
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.256-2376C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2593708 | ||||||
| chr4:2593741
|
C | G | 74 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.256-2343C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2593741 | ||||||
| chr4:2593850
|
G | C | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.256-2234G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2593850 | ||||||
| chr4:2593885
|
G | T | 1 | a0002c0006t0002g0105 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.256-2199G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2593885 | ||||||
| chr4:2593904
|
G | C | 1 | a0001c0001t0001g0293 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.256-2180G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2593904 | ||||||
| chr4:2594009
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.256-2075C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2594009 | ||||||
| chr4:2594310
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.256-1774C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2594310 | ||||||
| chr4:2594318
|
A | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.256-1766A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2594318 | ||||||
| chr4:2594351
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.256-1733G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2594351 | ||||||
| chr4:2594553
|
T | G | 1 | a0001c0001t0002g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.256-1531T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2594553 | ||||||
| chr4:2594566
|
C | T | 4 | a0001c0001t0001g0252a0001c0001t0001g0271a0001c0001t0001g0272others(1): Show | 4 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(1): Show |
intron_variant | MODIFIER | c.256-1518C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2594566 | ||||||
| chr4:2594581
|
C | T | 1 | a0001c0001t0002g0039 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.256-1503C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2594581 | ||||||
| chr4:2594815
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.256-1269T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2594815 | ||||||
| chr4:2594818
|
T | C | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.256-1266T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2594818 | ||||||
| chr4:2594820
|
C | CT | 92 | a0001c0001t0001g0122a0001c0001t0001g0241a0001c0001t0001g0243others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.256-1238dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2594820 | |||||
| chr4:2594820
|
C | CTT | 32 | a0001c0001t0001g0133a0001c0001t0001g0145a0001c0001t0001g0172others(29): Show | 32 | HG00408.hp1 HG01071.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.256-1239_256-1238d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2594820 | |||||
| chr4:2594820
|
C | CTTT | 62 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(59): Show | 62 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.256-1240_256-1238d others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2594820 | |||||
| chr4:2594820
|
C | CTTTT | 29 | a0001c0001t0001g0161a0001c0001t0001g0166a0001c0001t0001g0178others(26): Show | 29 | HG00738.hp2 HG01175.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.256-1241_256-1238d others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2594820 | |||||
| chr4:2594820
|
C | CTTTTT | 13 | a0001c0001t0001g0152a0001c0001t0001g0162a0001c0001t0001g0171others(10): Show | 13 | HG00609.hp2 HG01258.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.256-1242_256-1238d others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2594820 | |||||
| chr4:2594820
|
C | CTTTTTTT others(4): Show |
2 | a0007c0007t0001g0110a0007c0007t0003g0111 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.256-1248_256-1238d others(13): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 2594820 | |||||
| chr4:2594820
|
C | T | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.256-1264C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2594820 | ||||||
| chr4:2594865
|
A | G | 1 | a0001c0001t0002g0057 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.256-1219A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2594865 | ||||||
| chr4:2594891
|
T | C | 18 | a0001c0016t0001g0308a0003c0003t0001g0233a0003c0003t0001g0234others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.256-1193T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2594891 | ||||||
| chr4:2594932
|
G | T | 18 | a0001c0016t0001g0308a0003c0003t0001g0233a0003c0003t0001g0234others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.256-1152G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2594932 | ||||||
| chr4:2594961
|
T | C | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.256-1123T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2594961 | ||||||
| chr4:2595350
|
T | C | 18 | a0001c0016t0001g0308a0003c0003t0001g0233a0003c0003t0001g0234others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.256-734T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2595350 | ||||||
| chr4:2595650
|
G | C | 229 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0123others(226): Show | 229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.256-434G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2595650 | ||||||
| chr4:2595738
|
T | G | 1 | a0005c0005t0004g0141 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.256-346T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2595738 | ||||||
| chr4:2595754
|
C | T | 61 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0002t0001g0001others(58): Show | 61 | HG00408.hp1 HG00609.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.256-330C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 1/20 | chr4 | 2595754 | ||||||
| chr4:2596496
|
C | T | 1 | a0005c0005t0007g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.501+167C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2596496 | ||||||
| chr4:2596619
|
T | C | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.501+290T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2596619 | ||||||
| chr4:2596701
|
C | G | 1 | a0011c0023t0001g0247 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.501+372C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2596701 | ||||||
| chr4:2596719
|
T | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.501+390T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2596719 | ||||||
| chr4:2596743
|
C | CGAGGCCA others(4): Show |
231 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0123others(228): Show | 231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.501+424_501+425ins others(11): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2596743 | |||||
| chr4:2596745
|
A | AGGCCACA others(5): Show |
1 | a0001c0001t0004g0316 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.501+424_501+425ins others(12): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2596745 | |||||
| chr4:2596789
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.501+460T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2596789 | ||||||
| chr4:2596853
|
G | C | 4 | a0001c0001t0002g0073a0001c0001t0002g0079a0001c0001t0002g0093others(1): Show | 4 | NA18951.hp2 NA18983.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+524G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2596853 | ||||||
| chr4:2597061
|
A | G | 1 | a0004c0004t0001g0327 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.501+732A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2597061 | ||||||
| chr4:2597072
|
G | A | 79 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.501+743G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2597072 | ||||||
| chr4:2597185
|
G | A | 1 | a0001c0001t0012g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.501+856G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2597185 | ||||||
| chr4:2597221
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.501+892C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2597221 | ||||||
| chr4:2597471
|
C | G | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+1142C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2597471 | ||||||
| chr4:2597564
|
A | T | 1 | a0001c0001t0002g0048 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.501+1235A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2597564 | ||||||
| chr4:2597569
|
A | G | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+1240A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2597569 | ||||||
| chr4:2597651
|
G | A | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+1322G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2597651 | ||||||
| chr4:2597832
|
T | C | 56 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0002t0001g0001others(53): Show | 56 | HG00408.hp1 HG00609.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.501+1503T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2597832 | ||||||
| chr4:2597833
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.501+1504C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2597833 | ||||||
| chr4:2597855
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.501+1526C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2597855 | ||||||
| chr4:2597856
|
C | G | 1 | a0005c0005t0004g0140 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.501+1527C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2597856 | ||||||
| chr4:2597882
|
G | A | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.501+1553G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2597882 | ||||||
| chr4:2597906
|
C | A | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.501+1577C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2597906 | ||||||
| chr4:2598105
|
A | C | 1 | a0001c0001t0001g0174 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.501+1776A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2598105 | ||||||
| chr4:2598162
|
G | T | 1 | a0001c0001t0001g0292 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.501+1833G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2598162 | ||||||
| chr4:2598163
|
G | T | 1 | a0001c0001t0001g0292 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.501+1834G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2598163 | ||||||
| chr4:2598233
|
T | C | 1 | a0001c0001t0001g0300 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.501+1904T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2598233 | ||||||
| chr4:2598275
|
T | C | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+1946T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2598275 | ||||||
| chr4:2598277
|
C | T | 1 | a0002c0012t0004g0328 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.501+1948C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2598277 | ||||||
| chr4:2598298
|
G | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0276 | 2 | NA18951.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.501+1969G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2598298 | ||||||
| chr4:2598383
|
C | T | 6 | a0006c0008t0001g0121a0006c0008t0001g0125a0006c0008t0001g0126others(3): Show | 6 | HG02559.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.501+2054C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2598383 | ||||||
| chr4:2598394
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.501+2065T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2598394 | ||||||
| chr4:2598408
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.501+2079C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2598408 | ||||||
| chr4:2598477
|
A | G | 1 | a0001c0001t0002g0087 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.501+2148A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2598477 | ||||||
| chr4:2598482
|
A | AATGATTT others(29): Show |
1 | a0001c0001t0001g0206 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.501+2155_501+2190d others(38): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2598482 | |||||
| chr4:2598684
|
C | T | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.501+2355C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2598684 | ||||||
| chr4:2598742
|
T | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0166 | 2 | HG01175.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.501+2413T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2598742 | ||||||
| chr4:2598946
|
C | T | 4 | a0004c0004t0001g0321a0004c0004t0003g0317a0004c0004t0003g0319others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+2617C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2598946 | ||||||
| chr4:2599141
|
G | A | 1 | a0007c0007t0003g0118 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.501+2812G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2599141 | ||||||
| chr4:2599141
|
G | C | 14 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(11): Show | 14 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.501+2812G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2599141 | ||||||
| chr4:2599202
|
TTTAAAG | T | 11 | a0001c0001t0001g0122a0001c0001t0001g0133a0002c0012t0004g0328others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.501+2879_501+2884d others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2599202 | |||||
| chr4:2599216
|
G | GT | 6 | a0001c0001t0001g0170a0001c0001t0002g0012a0001c0001t0002g0015others(3): Show | 6 | HG01175.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.501+2899dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2599216 | |||||
| chr4:2599216
|
GT | G | 29 | a0001c0001t0001g0214a0001c0001t0002g0035a0001c0001t0002g0039others(26): Show | 29 | HG01928.hp1 HG02004.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.501+2899delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2599216 | |||||
| chr4:2599340
|
C | T | 14 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(11): Show | 14 | HG01167.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.501+3011C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2599340 | ||||||
| chr4:2599517
|
T | C | 1 | a0001c0002t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.501+3188T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2599517 | ||||||
| chr4:2599659
|
C | A | 1 | a0001c0001t0002g0015 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.501+3330C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2599659 | ||||||
| chr4:2599730
|
C | T | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.501+3401C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2599730 | ||||||
| chr4:2599739
|
G | GT | 18 | a0001c0001t0001g0290a0001c0001t0002g0012a0001c0001t0002g0022others(15): Show | 18 | HG01109.hp1 HG01109.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.501+3425dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2599739 | |||||
| chr4:2599739
|
GT | G | 74 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0144others(71): Show | 74 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.501+3425delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2599739 | |||||
| chr4:2599776
|
G | C | 4 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(1): Show | 4 | HG01891.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+3447G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2599776 | ||||||
| chr4:2599867
|
C | T | 1 | a0003c0003t0001g0235 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.501+3538C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2599867 | ||||||
| chr4:2599940
|
A | AC | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+3613dupC | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2599940 | |||||
| chr4:2600014
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.501+3685C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2600014 | ||||||
| chr4:2600260
|
A | C | 1 | a0001c0001t0002g0015 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.501+3931A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2600260 | ||||||
| chr4:2600289
|
G | C | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.501+3960G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2600289 | ||||||
| chr4:2600512
|
A | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.501+4183A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2600512 | ||||||
| chr4:2600698
|
G | GC | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.501+4372dupC | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2600698 | |||||
| chr4:2600745
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.501+4416C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2600745 | ||||||
| chr4:2600756
|
C | T | 1 | a0001c0001t0002g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.501+4427C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2600756 | ||||||
| chr4:2601004
|
C | T | 1 | a0001c0001t0007g0129 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.501+4675C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2601004 | ||||||
| chr4:2601115
|
G | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0040a0001c0001t0002g0047 | 3 | NA18967.hp1 NA19007.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.501+4786G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2601115 | ||||||
| chr4:2601227
|
C | CT | 142 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(139): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.501+4918dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2601227 | |||||
| chr4:2601227
|
C | CTT | 9 | a0001c0001t0001g0169a0001c0001t0001g0209a0001c0001t0001g0219others(6): Show | 9 | HG00544.hp2 HG01934.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.501+4917_501+4918d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2601227 | |||||
| chr4:2601227
|
CT | C | 19 | a0001c0001t0002g0012a0001c0001t0002g0014a0001c0001t0002g0026others(16): Show | 19 | HG00099.hp1 HG00140.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.501+4918delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2601227 | |||||
| chr4:2601228
|
T | TTC | 10 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.501+4900_501+4901i others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2601228 | |||||
| chr4:2601231
|
T | C | 1 | a0004c0004t0001g0327 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.501+4902T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2601231 | ||||||
| chr4:2601378
|
G | A | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.501+5049G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2601378 | ||||||
| chr4:2601391
|
C | G | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+5062C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2601391 | ||||||
| chr4:2601432
|
G | A | 2 | a0004c0004t0001g0323a0004c0004t0001g0327 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.501+5103G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2601432 | ||||||
| chr4:2601503
|
G | A | 4 | a0001c0001t0002g0011a0001c0001t0002g0040a0001c0001t0002g0047others(1): Show | 4 | NA18967.hp1 NA18970.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+5174G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2601503 | ||||||
| chr4:2601534
|
T | C | 11 | a0001c0001t0001g0122a0001c0001t0001g0133a0002c0012t0004g0328others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.501+5205T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2601534 | ||||||
| chr4:2601563
|
C | CT | 12 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+5242dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2601563 | |||||
| chr4:2601650
|
A | C | 1 | a0001c0001t0002g0015 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.501+5321A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2601650 | ||||||
| chr4:2601651
|
G | A | 1 | a0001c0001t0002g0015 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.501+5322G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2601651 | ||||||
| chr4:2601678
|
C | A | 1 | a0001c0001t0004g0316 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.501+5349C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2601678 | ||||||
| chr4:2601679
|
A | G | 1 | a0001c0001t0004g0316 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.501+5350A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2601679 | ||||||
| chr4:2601715
|
T | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.501+5386T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2601715 | ||||||
| chr4:2601725
|
TA | T | 7 | a0001c0001t0001g0163a0001c0001t0001g0206a0001c0001t0001g0290others(4): Show | 7 | HG01516.hp2 HG02615.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.501+5409delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2601725 | |||||
| chr4:2601726
|
A | T | 1 | a0001c0001t0004g0195 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.501+5397A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2601726 | ||||||
| chr4:2601748
|
A | C | 1 | a0001c0001t0001g0206 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.501+5419A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2601748 | ||||||
| chr4:2601839
|
TTTA | T | 5 | a0001c0001t0001g0255a0001c0001t0001g0259a0001c0001t0001g0282others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.501+5522_501+5524d others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2601839 | |||||
| chr4:2601900
|
G | A | 1 | a0003c0003t0004g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.501+5571G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2601900 | ||||||
| chr4:2601965
|
G | A | 233 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0123others(230): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.501+5636G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2601965 | ||||||
| chr4:2602052
|
T | C | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.501+5723T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2602052 | ||||||
| chr4:2602094
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.501+5765C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2602094 | ||||||
| chr4:2602118
|
C | T | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.501+5789C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2602118 | ||||||
| chr4:2602119
|
G | A | 1 | a0001c0001t0002g0035 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.501+5790G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2602119 | ||||||
| chr4:2602145
|
T | G | 1 | a0001c0001t0002g0019 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.501+5816T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2602145 | ||||||
| chr4:2602214
|
T | TA | 44 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(41): Show | 44 | HG00609.hp2 HG01243.hp2 HG01516.hp1 others(41): Show |
intron_variant | MODIFIER | c.501+5897dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2602214 | |||||
| chr4:2602214
|
T | TAA | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+5896_501+5897d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2602214 | |||||
| chr4:2602353
|
C | CT | 75 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0123others(72): Show | 75 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.501+6042dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2602353 | |||||
| chr4:2602353
|
C | CTT | 6 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0220others(3): Show | 6 | HG02486.hp2 HG03130.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.501+6041_501+6042d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2602353 | |||||
| chr4:2602353
|
CT | C | 24 | a0001c0001t0001g0152a0001c0001t0001g0226a0001c0001t0001g0232others(21): Show | 24 | HG01168.hp2 HG01496.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.501+6042delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2602353 | |||||
| chr4:2602438
|
T | A | 1 | a0005c0005t0004g0130 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.501+6109T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2602438 | ||||||
| chr4:2602519
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.501+6190A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2602519 | ||||||
| chr4:2602810
|
A | G | 1 | a0001c0002t0001g0240 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.501+6481A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2602810 | ||||||
| chr4:2602956
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.501+6627G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2602956 | ||||||
| chr4:2602959
|
C | CT | 16 | a0001c0001t0001g0133a0001c0001t0001g0177a0001c0001t0002g0008others(13): Show | 16 | HG00408.hp1 HG01074.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.501+6657dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2602959 | |||||
| chr4:2602959
|
C | CTT | 11 | a0001c0001t0001g0122a0001c0001t0002g0010a0003c0003t0001g0233others(8): Show | 11 | HG01884.hp1 HG01975.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.501+6656_501+6657d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2602959 | |||||
| chr4:2602959
|
C | CTTT | 14 | a0001c0021t0003g0143a0003c0003t0001g0234a0003c0003t0005g0164others(11): Show | 14 | HG00609.hp2 HG01891.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.501+6655_501+6657d others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2602959 | |||||
| chr4:2602959
|
C | CTTTT | 14 | a0001c0002t0016g0023a0001c0016t0001g0308a0003c0003t0005g0189others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.501+6654_501+6657d others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2602959 | |||||
| chr4:2602959
|
C | CTTTTTTT others(3): Show |
2 | a0001c0002t0009g0239a0003c0003t0004g0155 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.501+6648_501+6657d others(12): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2602959 | |||||
| chr4:2602959
|
C | CTTTTTTT others(4): Show |
3 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0240 | 3 | HG01243.hp2 HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.501+6647_501+6657d others(13): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2602959 | |||||
| chr4:2602959
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0232a0001c0002t0001g0001 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.501+6646_501+6657d others(14): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2602959 | |||||
| chr4:2602959
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0231 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.501+6645_501+6657d others(15): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2602959 | |||||
| chr4:2602959
|
CT | C | 141 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0142others(138): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.501+6657delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2602959 | |||||
| chr4:2602959
|
CTT | C | 62 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(59): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.501+6656_501+6657d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2602959 | |||||
| chr4:2602999
|
C | T | 3 | a0001c0002t0003g0112a0001c0002t0003g0120a0001c0002t0013g0117 | 3 | HG01516.hp1 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.501+6670C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2602999 | ||||||
| chr4:2603003
|
C | G | 1 | a0001c0001t0001g0213 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.501+6674C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2603003 | ||||||
| chr4:2603054
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.501+6725C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2603054 | ||||||
| chr4:2603069
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.501+6740C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2603069 | ||||||
| chr4:2603147
|
T | G | 1 | a0001c0002t0009g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.501+6818T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2603147 | ||||||
| chr4:2603167
|
TA | T | 14 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0016t0001g0308others(11): Show | 14 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.501+6839delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2603167 | ||||||
| chr4:2603228
|
G | T | 1 | a0001c0001t0001g0206 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.501+6899G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2603228 | ||||||
| chr4:2603229
|
C | G | 1 | a0001c0001t0001g0206 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.501+6900C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2603229 | ||||||
| chr4:2603263
|
T | C | 71 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0001t0001g0231others(68): Show | 71 | HG00408.hp1 HG00609.hp2 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.501+6934T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2603263 | ||||||
| chr4:2603275
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.501+6946C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2603275 | ||||||
| chr4:2603290
|
GT | G | 327 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(324): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.501+6972delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2603290 | |||||
| chr4:2603451
|
A | AT | 26 | a0001c0001t0001g0212a0001c0001t0001g0267a0001c0001t0001g0275others(23): Show | 26 | HG00140.hp2 HG00408.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.501+7145dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2603451 | |||||
| chr4:2603451
|
AT | A | 99 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(96): Show | 99 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.501+7145delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2603451 | |||||
| chr4:2603451
|
ATT | A | 16 | a0001c0001t0001g0179a0001c0001t0001g0231a0001c0001t0001g0232others(13): Show | 16 | HG01167.hp2 HG02145.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.501+7144_501+7145d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2603451 | |||||
| chr4:2603451
|
ATTTT | A | 9 | a0001c0001t0001g0122a0002c0012t0004g0328a0005c0005t0004g0128others(6): Show | 9 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.501+7142_501+7145d others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2603451 | |||||
| chr4:2603542
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.501+7213C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2603542 | ||||||
| chr4:2603811
|
C | T | 3 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0002g0044 | 3 | HG02602.hp2 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.501+7482C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2603811 | ||||||
| chr4:2603823
|
C | T | 77 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.501+7494C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2603823 | ||||||
| chr4:2604089
|
C | T | 12 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+7760C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2604089 | ||||||
| chr4:2604208
|
G | C | 1 | a0005c0005t0004g0128 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.501+7879G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2604208 | ||||||
| chr4:2604226
|
A | G | 5 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(2): Show | 5 | HG01891.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+7897A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2604226 | ||||||
| chr4:2604233
|
ACTGTATT others(2): Show |
A | 11 | a0001c0001t0001g0122a0001c0001t0001g0133a0002c0012t0004g0328others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.501+7916_501+7924d others(11): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2604233 | |||||
| chr4:2604343
|
CATTA | C | 14 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0030others(11): Show | 14 | HG00438.hp2 HG01934.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.501+8018_501+8021d others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2604343 | |||||
| chr4:2604434
|
G | A | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.501+8105G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2604434 | ||||||
| chr4:2604508
|
G | C | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.501+8179G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2604508 | ||||||
| chr4:2604591
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.501+8262G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2604591 | ||||||
| chr4:2604682
|
AT | A | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.501+8357delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2604682 | |||||
| chr4:2604724
|
A | G | 1 | a0001c0001t0007g0129 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.501+8395A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2604724 | ||||||
| chr4:2604732
|
T | A | 1 | a0005c0005t0004g0128 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.501+8403T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2604732 | ||||||
| chr4:2604791
|
C | CT | 26 | a0001c0001t0001g0151a0001c0001t0001g0166a0001c0001t0001g0193others(23): Show | 26 | HG00140.hp1 HG01175.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.501+8485dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2604791 | |||||
| chr4:2604791
|
CT | C | 28 | a0001c0001t0001g0146a0001c0001t0001g0204a0001c0001t0001g0241others(25): Show | 28 | HG01070.hp1 HG01243.hp2 HG01516.hp1 others(25): Show |
intron_variant | MODIFIER | c.501+8485delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2604791 | |||||
| chr4:2604791
|
CTT | C | 10 | a0004c0004t0001g0323a0004c0004t0001g0327a0006c0008t0001g0005others(7): Show | 10 | HG00609.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.501+8484_501+8485d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2604791 | |||||
| chr4:2604791
|
CTTT | C | 11 | a0001c0002t0013g0117a0001c0016t0001g0308a0004c0004t0001g0318others(8): Show | 11 | HG02257.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.501+8483_501+8485d others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2604791 | |||||
| chr4:2604791
|
CTTTT | C | 6 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0159others(3): Show | 6 | HG00438.hp1 NA18947.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.501+8482_501+8485d others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2604791 | |||||
| chr4:2604791
|
CTTTTTT | C | 12 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0001t0001g0245others(9): Show | 12 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+8480_501+8485d others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2604791 | |||||
| chr4:2604826
|
C | G | 3 | a0007c0007t0003g0106a0007c0007t0003g0107a0007c0007t0003g0108 | 3 | HG01891.hp1 HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.501+8497C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2604826 | ||||||
| chr4:2604981
|
A | T | 33 | a0001c0001t0001g0133a0001c0001t0001g0152a0001c0001t0001g0305others(30): Show | 33 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.501+8652A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2604981 | ||||||
| chr4:2605048
|
A | G | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.501+8719A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2605048 | ||||||
| chr4:2605158
|
G | C | 10 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(7): Show | 10 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.501+8829G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2605158 | ||||||
| chr4:2605254
|
C | A | 6 | a0003c0003t0005g0164a0003c0003t0005g0187a0003c0003t0005g0188others(3): Show | 6 | HG02257.hp2 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.501+8925C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2605254 | ||||||
| chr4:2605337
|
T | G | 1 | a0001c0002t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.501+9008T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2605337 | ||||||
| chr4:2605413
|
A | C | 1 | a0001c0002t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.501+9084A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2605413 | ||||||
| chr4:2605424
|
A | C | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.501+9095A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2605424 | ||||||
| chr4:2605487
|
C | T | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.501+9158C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2605487 | ||||||
| chr4:2605640
|
G | GT | 3 | a0001c0002t0003g0112a0001c0002t0003g0120a0001c0002t0013g0117 | 3 | HG01516.hp1 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.501+9316dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2605640 | |||||
| chr4:2605655
|
C | T | 1 | a0001c0018t0001g0260 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.501+9326C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2605655 | ||||||
| chr4:2605693
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.501+9364C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2605693 | ||||||
| chr4:2605700
|
G | A | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.501+9371G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2605700 | ||||||
| chr4:2605720
|
C | T | 1 | a0002c0006t0001g0242 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.501+9391C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2605720 | ||||||
| chr4:2605861
|
C | A | 11 | a0001c0001t0001g0122a0001c0001t0001g0133a0002c0012t0004g0328others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.501+9532C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2605861 | ||||||
| chr4:2605894
|
C | A | 1 | a0006c0008t0001g0132 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.501+9565C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2605894 | ||||||
| chr4:2605970
|
C | CA | 41 | a0001c0001t0001g0122a0001c0001t0001g0144a0001c0001t0001g0147others(38): Show | 41 | HG00438.hp1 HG00544.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.501+9669dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2605970 | |||||
| chr4:2605970
|
C | CAA | 11 | a0001c0001t0001g0123a0001c0001t0001g0142a0001c0001t0001g0151others(8): Show | 11 | HG01358.hp1 HG02630.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.501+9668_501+9669d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2605970 | |||||
| chr4:2605970
|
C | CAAA | 31 | a0001c0001t0001g0161a0001c0001t0001g0241a0001c0001t0001g0246others(28): Show | 31 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.501+9667_501+9669d others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2605970 | |||||
| chr4:2605970
|
C | CAAAA | 27 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0251others(24): Show | 27 | HG00099.hp2 HG00544.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.501+9666_501+9669d others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2605970 | |||||
| chr4:2605970
|
C | CAAAAA | 14 | a0001c0001t0001g0245a0001c0001t0001g0256a0001c0001t0001g0265others(11): Show | 14 | HG00140.hp2 HG00741.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.501+9665_501+9669d others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2605970 | |||||
| chr4:2605970
|
CA | C | 61 | a0001c0001t0001g0133a0001c0001t0001g0157a0001c0001t0001g0168others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.501+9669delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2605970 | |||||
| chr4:2605970
|
CAA | C | 15 | a0001c0001t0002g0021a0001c0001t0002g0061a0001c0001t0002g0329others(12): Show | 15 | HG01106.hp1 HG01243.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.501+9668_501+9669d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2605970 | |||||
| chr4:2605970
|
CAAA | C | 11 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0113others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.501+9667_501+9669d others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2605970 | |||||
| chr4:2605970
|
CAAAAAAA others(3): Show |
C | 14 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0016t0001g0308others(11): Show | 14 | HG01167.hp1 HG01496.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.501+9660_501+9669d others(12): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2605970 | |||||
| chr4:2605970
|
CAAAAAAA others(8): Show |
C | 5 | a0001c0001t0002g0011a0001c0001t0002g0034a0001c0001t0002g0040others(2): Show | 5 | NA18967.hp1 NA18970.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.501+9655_501+9669d others(17): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2605970 | |||||
| chr4:2605987
|
AAAAAAAA others(5): Show |
A | 1 | a0006c0008t0001g0125 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.501+9659_501+9670d others(14): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2605987 | ||||||
| chr4:2605996
|
A | G | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+9667A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2605996 | ||||||
| chr4:2605999
|
T | A | 7 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(4): Show | 7 | HG00609.hp2 HG02818.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.501+9670T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2605999 | ||||||
| chr4:2606045
|
C | CT | 51 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0001t0001g0163others(48): Show | 51 | HG00323.hp2 HG00408.hp1 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.501+9739dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2606045 | |||||
| chr4:2606045
|
C | CTT | 65 | a0001c0001t0001g0144a0001c0001t0001g0150a0001c0001t0001g0153others(62): Show | 65 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.501+9738_501+9739d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2606045 | |||||
| chr4:2606045
|
C | CTTT | 86 | a0001c0001t0001g0123a0001c0001t0001g0142a0001c0001t0001g0145others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.501+9737_501+9739d others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2606045 | |||||
| chr4:2606045
|
C | CTTTT | 25 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0202others(22): Show | 25 | HG00544.hp2 HG00741.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.501+9736_501+9739d others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2606045 | |||||
| chr4:2606298
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.501+9969C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2606298 | ||||||
| chr4:2606339
|
C | T | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.501+10010C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2606339 | ||||||
| chr4:2606342
|
A | G | 8 | a0001c0002t0016g0023a0007c0007t0001g0110a0007c0007t0003g0106others(5): Show | 8 | HG01891.hp1 HG02717.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.501+10013A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2606342 | ||||||
| chr4:2606387
|
C | G | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.501+10058C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2606387 | ||||||
| chr4:2606414
|
G | C | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.501+10085G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2606414 | ||||||
| chr4:2606592
|
T | C | 322 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(319): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.501+10263T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2606592 | ||||||
| chr4:2606745
|
T | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.501+10416T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2606745 | ||||||
| chr4:2606798
|
G | A | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.501+10469G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2606798 | ||||||
| chr4:2606818
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.501+10489G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2606818 | ||||||
| chr4:2607156
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.501+10827G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2607156 | ||||||
| chr4:2607253
|
T | TC | 11 | a0001c0001t0001g0122a0002c0012t0004g0328a0005c0005t0002g0138others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.501+10927dupC | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2607253 | |||||
| chr4:2607339
|
T | C | 11 | a0001c0001t0001g0122a0002c0012t0004g0328a0005c0005t0002g0138others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.501+11010T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2607339 | ||||||
| chr4:2607341
|
G | A | 5 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(2): Show | 5 | HG01891.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+11012G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2607341 | ||||||
| chr4:2607380
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.501+11051C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2607380 | ||||||
| chr4:2607384
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.501+11055G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2607384 | ||||||
| chr4:2607450
|
G | T | 1 | a0001c0001t0001g0298 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.501+11121G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2607450 | ||||||
| chr4:2607569
|
A | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0309a0001c0001t0001g0311 | 3 | NA18940.hp1 NA18959.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.501+11240A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2607569 | ||||||
| chr4:2607612
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.501+11283C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2607612 | ||||||
| chr4:2607817
|
T | C | 10 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(7): Show | 10 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.501+11488T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2607817 | ||||||
| chr4:2607938
|
C | G | 1 | a0001c0001t0002g0062 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.501+11609C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2607938 | ||||||
| chr4:2608042
|
T | C | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+11713T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2608042 | ||||||
| chr4:2608075
|
G | A | 1 | a0007c0007t0003g0118 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.501+11746G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2608075 | ||||||
| chr4:2608202
|
C | T | 11 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(8): Show | 11 | HG01891.hp2 HG02559.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.501+11873C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2608202 | ||||||
| chr4:2608265
|
AC | A | 4 | a0004c0004t0001g0321a0004c0004t0003g0317a0004c0004t0003g0319others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+11938delC | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2608265 | |||||
| chr4:2608326
|
G | A | 1 | a0001c0001t0002g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.501+11997G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2608326 | ||||||
| chr4:2608369
|
G | A | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+12040G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2608369 | ||||||
| chr4:2608473
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.501+12144A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2608473 | ||||||
| chr4:2608538
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.501+12209T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2608538 | ||||||
| chr4:2608563
|
G | T | 1 | a0001c0001t0004g0196 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.501+12234G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2608563 | ||||||
| chr4:2608666
|
A | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.501+12337A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2608666 | ||||||
| chr4:2608681
|
C | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.501+12352C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2608681 | ||||||
| chr4:2608815
|
G | T | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.501+12486G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2608815 | ||||||
| chr4:2608854
|
C | G | 2 | a0001c0021t0003g0143a0014c0024t0018g0139 | 2 | HG01884.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.501+12525C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2608854 | ||||||
| chr4:2608858
|
C | T | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.501+12529C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2608858 | ||||||
| chr4:2608892
|
C | CT | 17 | a0001c0001t0001g0170a0001c0001t0001g0280a0001c0002t0001g0001others(14): Show | 17 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.501+12579dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2608892 | |||||
| chr4:2608892
|
C | CTT | 6 | a0001c0002t0003g0112a0001c0002t0003g0116a0001c0002t0003g0120others(3): Show | 6 | HG01516.hp1 HG02615.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.501+12578_501+1257 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2608892 | |||||
| chr4:2608904
|
T | C | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+12575T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2608904 | ||||||
| chr4:2609013
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.501+12684C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2609013 | ||||||
| chr4:2609080
|
G | A | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.501+12751G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2609080 | ||||||
| chr4:2609139
|
G | A | 5 | a0001c0001t0001g0165a0001c0001t0001g0197a0001c0001t0001g0198others(2): Show | 5 | HG00738.hp2 HG01257.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.501+12810G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2609139 | ||||||
| chr4:2609175
|
AGCCACC | A | 3 | a0001c0001t0001g0261a0001c0001t0001g0265a0001c0001t0001g0289 | 3 | HG02165.hp1 NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.501+12848_501+1285 others(10): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2609175 | |||||
| chr4:2609290
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.501+12961A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2609290 | ||||||
| chr4:2609329
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.501+13000C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2609329 | ||||||
| chr4:2609452
|
A | C | 1 | a0001c0002t0001g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.501+13123A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2609452 | ||||||
| chr4:2609666
|
A | T | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.501+13337A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2609666 | ||||||
| chr4:2609696
|
G | A | 2 | a0001c0001t0001g0303a0006c0008t0001g0121 | 2 | HG01070.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.501+13367G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2609696 | ||||||
| chr4:2609927
|
T | TA | 6 | a0001c0001t0001g0193a0001c0001t0002g0011a0001c0001t0002g0015others(3): Show | 6 | HG02486.hp2 HG03130.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.501+13611dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2609927 | |||||
| chr4:2609977
|
A | G | 1 | a0002c0006t0001g0287 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.501+13648A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2609977 | ||||||
| chr4:2610151
|
G | C | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.501+13822G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2610151 | ||||||
| chr4:2610261
|
A | G | 1 | a0005c0005t0004g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.501+13932A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2610261 | ||||||
| chr4:2610295
|
G | T | 2 | a0001c0001t0002g0024a0001c0001t0002g0025 | 2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.501+13966G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2610295 | ||||||
| chr4:2610331
|
C | T | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.501+14002C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2610331 | ||||||
| chr4:2610337
|
T | TA | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.501+14011dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2610337 | |||||
| chr4:2610394
|
T | C | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.501+14065T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2610394 | ||||||
| chr4:2610652
|
A | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.501+14323A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2610652 | ||||||
| chr4:2610675
|
G | C | 1 | a0001c0001t0001g0177 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.501+14346G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2610675 | ||||||
| chr4:2610729
|
A | T | 2 | a0002c0011t0003g0114a0007c0007t0001g0115 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.501+14400A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2610729 | ||||||
| chr4:2610798
|
C | T | 6 | a0001c0001t0002g0017a0001c0001t0002g0032a0001c0001t0002g0033others(3): Show | 6 | HG00558.hp2 HG01074.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.502-14464C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2610798 | ||||||
| chr4:2610819
|
C | G | 3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | NA18945.hp2 NA18983.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.502-14443C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2610819 | ||||||
| chr4:2611100
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.502-14162G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2611100 | ||||||
| chr4:2611256
|
A | C | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.502-14006A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2611256 | ||||||
| chr4:2611261
|
C | CTATT | 10 | a0004c0004t0001g0323a0004c0004t0001g0327a0006c0008t0001g0005others(7): Show | 10 | HG00609.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.502-13979_502-1397 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2611261 | |||||
| chr4:2611332
|
A | C | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.502-13930A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2611332 | ||||||
| chr4:2611369
|
A | G | 1 | a0001c0001t0002g0034 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.502-13893A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2611369 | ||||||
| chr4:2611382
|
T | C | 56 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(53): Show | 56 | HG00609.hp2 HG01243.hp2 HG01516.hp1 others(53): Show |
intron_variant | MODIFIER | c.502-13880T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2611382 | ||||||
| chr4:2611466
|
G | A | 1 | a0001c0001t0012g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.502-13796G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2611466 | ||||||
| chr4:2611510
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.502-13752G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2611510 | ||||||
| chr4:2611565
|
C | T | 1 | a0001c0001t0002g0013 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.502-13697C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2611565 | ||||||
| chr4:2611592
|
C | T | 4 | a0001c0001t0001g0257a0001c0001t0001g0309a0001c0001t0001g0311others(1): Show | 4 | HG02015.hp1 NA18940.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.502-13670C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2611592 | ||||||
| chr4:2611770
|
G | C | 6 | a0006c0008t0001g0121a0006c0008t0001g0125a0006c0008t0001g0126others(3): Show | 6 | HG02559.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.502-13492G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2611770 | ||||||
| chr4:2611838
|
A | AT | 33 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(30): Show | 33 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.502-13408dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2611838 | |||||
| chr4:2611838
|
AT | A | 16 | a0001c0001t0001g0122a0001c0001t0001g0133a0001c0001t0002g0010others(13): Show | 16 | HG00408.hp2 HG00673.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.502-13408delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2611838 | |||||
| chr4:2611916
|
A | C | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.502-13346A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2611916 | ||||||
| chr4:2611982
|
G | A | 78 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(75): Show | 78 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.502-13280G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2611982 | ||||||
| chr4:2612271
|
A | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-12991A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2612271 | ||||||
| chr4:2612503
|
C | A | 19 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(16): Show | 19 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.502-12759C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2612503 | ||||||
| chr4:2612532
|
T | C | 5 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(2): Show | 5 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.502-12730T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2612532 | ||||||
| chr4:2612644
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-12618C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2612644 | ||||||
| chr4:2612747
|
C | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-12515C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2612747 | ||||||
| chr4:2612860
|
A | G | 3 | a0001c0002t0003g0112a0001c0002t0003g0120a0001c0002t0013g0117 | 3 | HG01516.hp1 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.502-12402A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2612860 | ||||||
| chr4:2612958
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.502-12304C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2612958 | ||||||
| chr4:2613177
|
C | T | 6 | a0006c0008t0001g0121a0006c0008t0001g0125a0006c0008t0001g0126others(3): Show | 6 | HG02559.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.502-12085C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2613177 | ||||||
| chr4:2613300
|
A | G | 4 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(1): Show | 4 | HG01891.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-11962A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2613300 | ||||||
| chr4:2613378
|
C | CT | 30 | a0001c0001t0001g0122a0001c0001t0001g0152a0001c0001t0001g0166others(27): Show | 30 | HG00323.hp2 HG00408.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.502-11867dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2613378 | |||||
| chr4:2613378
|
CT | C | 23 | a0001c0001t0001g0165a0001c0001t0001g0197a0001c0001t0001g0198others(20): Show | 23 | HG00738.hp2 HG01106.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.502-11867delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2613378 | |||||
| chr4:2613459
|
C | CT | 14 | a0001c0001t0001g0206a0001c0001t0002g0058a0001c0001t0002g0071others(11): Show | 14 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.502-11790dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2613459 | |||||
| chr4:2613753
|
C | CT | 12 | a0001c0001t0001g0122a0001c0021t0003g0143a0002c0012t0004g0328others(9): Show | 12 | HG00408.hp1 HG01074.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.502-11495dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2613753 | |||||
| chr4:2613753
|
CT | C | 200 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(197): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.502-11495delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2613753 | |||||
| chr4:2613767
|
TC | T | 10 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.502-11494delC | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2613767 | ||||||
| chr4:2613768
|
C | T | 1 | a0004c0004t0003g0320 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.502-11494C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2613768 | ||||||
| chr4:2613774
|
CT | C | 214 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0123others(211): Show | 214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.502-11478delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2613774 | |||||
| chr4:2613900
|
G | T | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.502-11362G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2613900 | ||||||
| chr4:2613963
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.502-11299C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2613963 | ||||||
| chr4:2613990
|
G | A | 1 | a0001c0002t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.502-11272G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2613990 | ||||||
| chr4:2614021
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.502-11241C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2614021 | ||||||
| chr4:2614027
|
C | G | 1 | a0003c0003t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.502-11235C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2614027 | ||||||
| chr4:2614075
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.502-11187C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2614075 | ||||||
| chr4:2614165
|
A | G | 5 | a0003c0003t0005g0164a0003c0003t0005g0187a0003c0003t0005g0188others(2): Show | 5 | HG02257.hp2 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-11097A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2614165 | ||||||
| chr4:2614217
|
A | G | 231 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0123others(228): Show | 231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.502-11045A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2614217 | ||||||
| chr4:2614331
|
A | G | 1 | a0001c0001t0002g0092 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.502-10931A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2614331 | ||||||
| chr4:2614475
|
G | A | 83 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(80): Show | 83 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.502-10787G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2614475 | ||||||
| chr4:2614642
|
T | G | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.502-10620T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2614642 | ||||||
| chr4:2614967
|
G | T | 1 | a0001c0001t0001g0209 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.502-10295G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2614967 | ||||||
| chr4:2615000
|
G | A | 75 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.502-10262G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2615000 | ||||||
| chr4:2615074
|
T | G | 22 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(19): Show | 22 | HG00609.hp2 HG02145.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.502-10188T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2615074 | ||||||
| chr4:2615475
|
T | G | 1 | a0006c0008t0001g0127 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.502-9787T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2615475 | ||||||
| chr4:2615563
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.502-9699G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2615563 | ||||||
| chr4:2615751
|
T | G | 3 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0002g0048 | 3 | HG01071.hp2 HG02004.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.502-9511T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2615751 | ||||||
| chr4:2615763
|
G | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0231a0001c0001t0001g0232 | 3 | HG02647.hp1 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.502-9499G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2615763 | ||||||
| chr4:2615776
|
G | A | 3 | a0001c0001t0001g0255a0001c0001t0001g0259a0002c0006t0001g0242 | 3 | HG02055.hp1 HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.502-9486G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2615776 | ||||||
| chr4:2615873
|
C | A | 1 | a0001c0001t0001g0300 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.502-9389C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2615873 | ||||||
| chr4:2615934
|
T | C | 12 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.502-9328T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2615934 | ||||||
| chr4:2615977
|
A | G | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.502-9285A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2615977 | ||||||
| chr4:2616002
|
T | C | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-9260T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2616002 | ||||||
| chr4:2616100
|
G | A | 1 | a0001c0002t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.502-9162G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2616100 | ||||||
| chr4:2616276
|
A | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-8986A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2616276 | ||||||
| chr4:2616465
|
T | C | 1 | a0001c0001t0002g0063 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.502-8797T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2616465 | ||||||
| chr4:2616542
|
C | T | 1 | a0003c0003t0001g0236 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.502-8720C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2616542 | ||||||
| chr4:2616618
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.502-8644C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2616618 | ||||||
| chr4:2616691
|
C | A | 4 | a0001c0001t0001g0163a0001c0001t0001g0181a0001c0001t0001g0182others(1): Show | 4 | NA18945.hp2 NA18983.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-8571C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2616691 | ||||||
| chr4:2616940
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-8322G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2616940 | ||||||
| chr4:2616943
|
C | T | 1 | a0001c0001t0002g0098 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.502-8319C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2616943 | ||||||
| chr4:2617047
|
C | A | 227 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0123others(224): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.502-8215C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617047 | ||||||
| chr4:2617168
|
C | CA | 16 | a0001c0001t0001g0304a0001c0001t0002g0059a0003c0003t0004g0155others(13): Show | 16 | HG00609.hp2 HG02074.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.502-8081dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617168 | |||||
| chr4:2617168
|
CAAAAAAA others(9): Show |
C | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-8080_502-8065d others(18): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617168 | |||||
| chr4:2617183
|
T | TA | 11 | a0001c0001t0001g0122a0001c0021t0003g0143a0002c0012t0004g0328others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-8065dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617183 | |||||
| chr4:2617212
|
C | T | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.502-8050C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617212 | ||||||
| chr4:2617239
|
A | ATTTT | 3 | a0007c0007t0003g0106a0007c0007t0003g0107a0007c0007t0003g0108 | 3 | HG01891.hp1 HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.502-8021_502-8020i others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617239 | |||||
| chr4:2617240
|
T | TTA | 12 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.502-8000_502-7999d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617240 | |||||
| chr4:2617240
|
T | TTTTATAT others(11): Show |
1 | a0001c0001t0008g0249 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.502-8021_502-8020i others(20): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617240 | |||||
| chr4:2617240
|
T | TTTTTTAT others(11): Show |
1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.502-8021_502-8020i others(20): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617240 | |||||
| chr4:2617242
|
A | T | 221 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0123others(218): Show | 221 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.502-8020A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617242 | ||||||
| chr4:2617258
|
A | T | 1 | a0001c0001t0002g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.502-8004A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617258 | ||||||
| chr4:2617260
|
A | ATTTTATA others(60): Show |
1 | a0003c0003t0005g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.502-8001_502-8000i others(69): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617260 | |||||
| chr4:2617260
|
A | ATTTTATA others(57): Show |
1 | a0003c0003t0005g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.502-8001_502-8000i others(66): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617260 | |||||
| chr4:2617260
|
A | ATTTTATA others(59): Show |
1 | a0003c0003t0005g0164 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.502-8001_502-8000i others(68): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617260 | |||||
| chr4:2617260
|
A | ATTTTATA others(57): Show |
1 | a0003c0003t0005g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.502-8001_502-8000i others(66): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617260 | |||||
| chr4:2617260
|
A | ATTTTATA others(51): Show |
1 | a0003c0003t0005g0187 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.502-8001_502-8000i others(60): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617260 | |||||
| chr4:2617260
|
A | ATTTTATA others(52): Show |
1 | a0003c0003t0011g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.502-8001_502-8000i others(61): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617260 | |||||
| chr4:2617260
|
A | T | 1 | a0001c0001t0002g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.502-8002A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617260 | ||||||
| chr4:2617262
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0156 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(15): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0300 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(17): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(44): Show |
1 | a0001c0002t0001g0001 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(53): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(44): Show |
1 | a0001c0002t0003g0120 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(53): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(40): Show |
1 | a0001c0002t0001g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(49): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(41): Show |
1 | a0001c0002t0013g0117 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(50): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(43): Show |
1 | a0005c0005t0004g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(52): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(72): Show |
1 | a0001c0002t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(81): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(39): Show |
2 | a0001c0002t0001g0002a0005c0005t0004g0135 | 2 | HG01074.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(48): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(46): Show |
1 | a0001c0001t0001g0122 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(55): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(36): Show |
2 | a0002c0011t0003g0114a0004c0004t0001g0327 | 2 | HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(45): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(37): Show |
2 | a0003c0003t0004g0155a0007c0007t0003g0111 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(46): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(41): Show |
1 | a0005c0005t0004g0136 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(50): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(44): Show |
1 | a0007c0007t0003g0109 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(53): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(31): Show |
2 | a0001c0002t0016g0023a0007c0007t0001g0115 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(40): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(33): Show |
1 | a0001c0002t0001g0240 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(42): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(38): Show |
1 | a0007c0007t0003g0106 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(47): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(40): Show |
1 | a0007c0007t0003g0107 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(49): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(42): Show |
1 | a0005c0005t0007g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(51): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(29): Show |
1 | a0002c0012t0004g0328 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(38): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(32): Show |
1 | a0004c0004t0001g0323 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(41): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(35): Show |
1 | a0005c0005t0004g0140 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(44): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(37): Show |
1 | a0007c0007t0003g0108 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(46): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(41): Show |
1 | a0003c0003t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(50): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(19): Show |
1 | a0002c0006t0001g0242 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(28): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(38): Show |
1 | a0003c0003t0001g0236 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(47): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0176 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(26): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(18): Show |
1 | a0004c0004t0001g0322 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(27): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(22): Show |
2 | a0001c0001t0001g0160a0001c0001t0001g0166 | 2 | HG01175.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(31): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(26): Show |
1 | a0005c0005t0004g0141 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(35): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0231 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(23): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0255a0001c0001t0001g0279 | 2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(26): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(19): Show |
1 | a0003c0003t0001g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(28): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(20): Show |
2 | a0001c0001t0001g0174a0001c0002t0009g0239 | 2 | HG02818.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(29): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(24): Show |
2 | a0007c0007t0001g0110a0007c0007t0003g0118 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(33): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(36): Show |
1 | a0003c0003t0001g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(45): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0226 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(21): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(22): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(14): Show |
1 | a0004c0004t0001g0318 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(23): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0169a0001c0001t0002g0048 | 2 | HG01071.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(24): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0285 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(25): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(17): Show |
1 | a0004c0004t0001g0321 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(26): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(18): Show |
4 | a0001c0001t0001g0142a0001c0001t0001g0151a0001c0001t0001g0184others(1): Show | 4 | HG00438.hp1 HG01358.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(27): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0144 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(29): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(23): Show |
1 | a0001c0002t0003g0112 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(32): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(34): Show |
1 | a0003c0003t0001g0235 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(43): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0177a0001c0001t0001g0225a0001c0001t0001g0232others(1): Show | 4 | HG02451.hp1 HG03017.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(19): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(13): Show |
5 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0175others(2): Show | 5 | HG02622.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(22): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(14): Show |
2 | a0006c0008t0001g0121a0006c0008t0001g0127 | 2 | HG02818.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(23): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0193 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(24): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0159a0006c0008t0001g0132 | 2 | NA19030.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(25): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(26): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0223a0001c0025t0001g0224 | 2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(18): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0158a0001c0001t0001g0173a0001c0001t0003g0154others(1): Show | 4 | HG00642.hp1 HG01167.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(19): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0007g0137 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(20): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(12): Show |
4 | a0001c0001t0001g0213a0001c0001t0001g0219a0001c0001t0010g0149others(1): Show | 4 | HG01361.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(21): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(13): Show |
3 | a0001c0001t0001g0199a0001c0001t0001g0206a0006c0008t0001g0216 | 3 | HG00738.hp2 HG02895.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(22): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(14): Show |
11 | a0001c0001t0001g0153a0001c0001t0001g0163a0001c0001t0001g0181others(8): Show | 11 | HG01109.hp1 HG03688.hp1 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(23): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0167a0001c0001t0001g0185 | 2 | HG01081.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(24): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0203 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(25): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(21): Show |
1 | a0005c0005t0004g0130 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(30): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0172 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(16): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(18): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0282a0001c0001t0001g0296 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(20): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(12): Show |
5 | a0001c0001t0001g0161a0001c0001t0001g0179a0001c0001t0001g0250others(2): Show | 5 | HG02083.hp2 HG02145.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(21): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(13): Show |
17 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0150others(14): Show | 17 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(22): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(14): Show |
7 | a0001c0001t0001g0123a0001c0001t0001g0145a0001c0001t0001g0198others(4): Show | 7 | HG00609.hp2 HG03654.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(23): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(15): Show |
7 | a0001c0001t0001g0004a0001c0001t0001g0162a0001c0001t0001g0165others(4): Show | 7 | HG00544.hp1 HG01257.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(24): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(7): Show |
1 | a0006c0008t0001g0125 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(16): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0253a0004c0004t0001g0325a0004c0004t0001g0326 | 3 | HG01167.hp1 HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(17): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(9): Show |
4 | a0001c0001t0001g0211a0001c0001t0001g0252a0001c0001t0001g0271others(1): Show | 4 | HG00323.hp1 HG00733.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(18): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0248a0001c0001t0001g0265a0001c0001t0001g0273others(1): Show | 4 | HG01168.hp2 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(19): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(11): Show |
5 | a0001c0001t0001g0261a0001c0001t0001g0272a0001c0001t0001g0304others(2): Show | 5 | HG00280.hp1 HG02004.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(20): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(12): Show |
5 | a0001c0001t0001g0180a0001c0001t0001g0201a0001c0001t0001g0210others(2): Show | 5 | HG00609.hp1 HG02040.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(21): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0171 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(23): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(8): Show |
10 | a0001c0001t0001g0246a0001c0001t0001g0254a0001c0001t0001g0263others(7): Show | 10 | HG00140.hp2 HG00741.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(17): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0293 | 3 | HG02165.hp1 HG02602.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(18): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0276a0008c0009t0001g0266 | 2 | NA18944.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(19): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0297 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(20): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0264 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(21): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0002g0095 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(22): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATTT others(5): Show |
1 | a0009c0010t0014g0228 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(14): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATTT others(6): Show |
1 | a0009c0010t0015g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(15): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATTT others(7): Show |
1 | a0001c0001t0001g0277 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(16): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATTT others(8): Show |
7 | a0001c0001t0001g0245a0001c0001t0001g0258a0001c0001t0001g0284others(4): Show | 7 | HG01106.hp2 HG02523.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(17): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATTT others(9): Show |
5 | a0001c0001t0001g0241a0001c0001t0001g0275a0001c0001t0001g0307others(2): Show | 5 | HG02056.hp1 HG02523.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(18): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATTT others(10): Show |
5 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0306others(2): Show | 5 | HG00099.hp2 HG02135.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.502-7999_502-7998i others(19): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATTT others(11): Show |
2 | a0001c0001t0001g0257a0002c0006t0001g0268 | 2 | HG00544.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(20): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATATTT others(12): Show |
2 | a0001c0001t0001g0309a0001c0018t0001g0260 | 2 | HG00735.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(21): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATTTTT others(7): Show |
1 | a0001c0001t0001g0313 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(16): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATTTTT others(9): Show |
2 | a0001c0001t0001g0267a0001c0001t0001g0311 | 2 | NA18940.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(18): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATTTTT others(10): Show |
1 | a0008c0009t0001g0310 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(19): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATATTTTT others(11): Show |
1 | a0008c0009t0001g0295 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.502-7999_502-7998i others(20): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0012g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.502-7991_502-7978d others(16): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | ATTTTTTT others(8): Show |
2 | a0001c0001t0001g0303a0001c0001t0001g0312 | 2 | HG01070.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.502-7992_502-7978d others(17): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2617262 | |||||
| chr4:2617262
|
A | T | 22 | a0001c0001t0001g0065a0001c0001t0002g0009a0001c0001t0002g0013others(19): Show | 22 | HG00673.hp2 HG01081.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.502-8000A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617262 | ||||||
| chr4:2617263
|
T | TA | 3 | a0001c0001t0002g0014a0001c0021t0003g0143a0005c0005t0002g0138 | 3 | HG00140.hp1 HG02572.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.502-7999_502-7998i others(3): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617263 | ||||||
| chr4:2617263
|
T | TATATATA others(8): Show |
1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(17): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617263 | ||||||
| chr4:2617263
|
T | TATATATA others(10): Show |
1 | a0004c0017t0001g0324 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.502-7999_502-7998i others(19): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617263 | ||||||
| chr4:2617264
|
T | A | 10 | a0001c0001t0002g0006a0001c0001t0002g0041a0001c0001t0002g0045others(7): Show | 10 | HG01257.hp1 HG01258.hp1 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.502-7998T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617264 | ||||||
| chr4:2617265
|
T | A | 5 | a0001c0001t0002g0081a0001c0021t0003g0143a0004c0017t0001g0324others(2): Show | 5 | HG01884.hp1 HG02572.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-7997T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617265 | ||||||
| chr4:2617267
|
T | A | 1 | a0004c0017t0001g0324 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.502-7995T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617267 | ||||||
| chr4:2617359
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-7903G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617359 | ||||||
| chr4:2617453
|
G | C | 1 | a0001c0018t0001g0260 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.502-7809G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617453 | ||||||
| chr4:2617487
|
A | G | 9 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(6): Show | 9 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.502-7775A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617487 | ||||||
| chr4:2617512
|
C | T | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.502-7750C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617512 | ||||||
| chr4:2617518
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.502-7744C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617518 | ||||||
| chr4:2617544
|
A | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-7718A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617544 | ||||||
| chr4:2617581
|
C | G | 5 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(2): Show | 5 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.502-7681C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617581 | ||||||
| chr4:2617614
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-7648G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617614 | ||||||
| chr4:2617615
|
T | C | 2 | a0001c0001t0001g0277a0001c0001t0001g0281 | 2 | NA18957.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.502-7647T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617615 | ||||||
| chr4:2617638
|
A | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.502-7624A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617638 | ||||||
| chr4:2617647
|
C | T | 1 | a0005c0005t0004g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.502-7615C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617647 | ||||||
| chr4:2617750
|
G | C | 1 | a0001c0018t0001g0260 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.502-7512G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617750 | ||||||
| chr4:2617982
|
G | A | 227 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0123others(224): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.502-7280G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2617982 | ||||||
| chr4:2618122
|
C | CATAT | 7 | a0007c0007t0001g0110a0007c0007t0003g0106a0007c0007t0003g0107others(4): Show | 7 | HG01891.hp1 HG02717.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.502-7139_502-7136d others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2618122 | |||||
| chr4:2618451
|
A | T | 20 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(17): Show | 20 | HG00609.hp2 HG01891.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.502-6811A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2618451 | ||||||
| chr4:2618483
|
G | A | 12 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.502-6779G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2618483 | ||||||
| chr4:2618591
|
C | CT | 106 | a0001c0001t0001g0173a0001c0001t0001g0241a0001c0001t0001g0243others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.502-6650dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2618591 | |||||
| chr4:2618591
|
C | CTT | 11 | a0001c0001t0001g0250a0001c0001t0001g0258a0001c0001t0001g0275others(8): Show | 11 | HG00544.hp2 HG01106.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-6651_502-6650d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2618591 | |||||
| chr4:2618636
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.502-6626C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2618636 | ||||||
| chr4:2618642
|
C | A | 1 | a0001c0001t0002g0069 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.502-6620C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2618642 | ||||||
| chr4:2618723
|
G | T | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.502-6539G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2618723 | ||||||
| chr4:2618777
|
A | T | 314 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(311): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.502-6485A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2618777 | ||||||
| chr4:2618843
|
C | T | 1 | a0001c0002t0001g0240 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.502-6419C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2618843 | ||||||
| chr4:2618884
|
C | T | 1 | a0010c0022t0001g0227 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.502-6378C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2618884 | ||||||
| chr4:2619022
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.502-6240G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2619022 | ||||||
| chr4:2619093
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.502-6169G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2619093 | ||||||
| chr4:2619186
|
T | TCCCATCG others(26): Show |
1 | a0001c0001t0002g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.502-6074_502-6042d others(35): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2619186 | |||||
| chr4:2619230
|
T | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-6032T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2619230 | ||||||
| chr4:2619372
|
G | A | 1 | a0001c0001t0002g0104 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.502-5890G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2619372 | ||||||
| chr4:2619386
|
T | C | 1 | a0001c0001t0002g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.502-5876T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2619386 | ||||||
| chr4:2619450
|
G | A | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.502-5812G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2619450 | ||||||
| chr4:2619507
|
T | A | 41 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(38): Show | 41 | HG00609.hp2 HG01243.hp2 HG01516.hp1 others(38): Show |
intron_variant | MODIFIER | c.502-5755T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2619507 | ||||||
| chr4:2619526
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-5736G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2619526 | ||||||
| chr4:2619588
|
G | A | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.502-5674G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2619588 | ||||||
| chr4:2619659
|
G | A | 1 | a0003c0003t0004g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.502-5603G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2619659 | ||||||
| chr4:2619749
|
G | A | 3 | a0001c0002t0003g0112a0001c0002t0003g0120a0001c0002t0013g0117 | 3 | HG01516.hp1 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.502-5513G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2619749 | ||||||
| chr4:2619811
|
C | G | 1 | a0001c0001t0002g0085 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.502-5451C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2619811 | ||||||
| chr4:2620030
|
T | C | 6 | a0003c0003t0005g0164a0003c0003t0005g0187a0003c0003t0005g0188others(3): Show | 6 | HG02257.hp2 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.502-5232T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2620030 | ||||||
| chr4:2620238
|
C | G | 66 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(63): Show | 66 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.502-5024C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2620238 | ||||||
| chr4:2620248
|
T | C | 3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | NA18945.hp2 NA18983.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.502-5014T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2620248 | ||||||
| chr4:2620423
|
A | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.502-4839A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2620423 | ||||||
| chr4:2620514
|
C | G | 1 | a0001c0001t0002g0048 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.502-4748C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2620514 | ||||||
| chr4:2620576
|
T | TG | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-4685dupG | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2620576 | |||||
| chr4:2620708
|
G | GGGT | 78 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.502-4545_502-4543d others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2620708 | |||||
| chr4:2620745
|
A | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.502-4517A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2620745 | ||||||
| chr4:2620836
|
C | CA | 19 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0011others(16): Show | 19 | HG01243.hp1 HG01928.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.502-4404dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2620836 | |||||
| chr4:2620836
|
C | CAAAA | 7 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(4): Show | 7 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.502-4407_502-4404d others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2620836 | |||||
| chr4:2620836
|
C | CAAAAAAA others(1): Show |
6 | a0007c0007t0003g0106a0007c0007t0003g0107a0007c0007t0003g0108others(3): Show | 6 | HG01891.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.502-4411_502-4404d others(10): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2620836 | |||||
| chr4:2620836
|
C | CAAAAAAA others(10): Show |
2 | a0001c0002t0016g0023a0007c0007t0001g0115 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.502-4420_502-4404d others(19): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2620836 | |||||
| chr4:2620836
|
C | CAAAAAAA others(12): Show |
4 | a0001c0002t0003g0112a0001c0002t0003g0119a0001c0002t0003g0120others(1): Show | 4 | HG01516.hp1 HG02615.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-4422_502-4404d others(21): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2620836 | |||||
| chr4:2620836
|
C | CAAAAAAA others(13): Show |
1 | a0001c0002t0003g0116 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.502-4423_502-4404d others(22): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2620836 | |||||
| chr4:2620836
|
C | CAAAAAAA others(16): Show |
1 | a0001c0002t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.502-4404_502-4403i others(25): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2620836 | |||||
| chr4:2620836
|
C | CAAAAAAA others(18): Show |
1 | a0001c0002t0013g0117 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.502-4404_502-4403i others(27): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2620836 | |||||
| chr4:2620836
|
C | CAAAAAAA others(24): Show |
1 | a0001c0002t0009g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.502-4404_502-4403i others(33): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2620836 | |||||
| chr4:2620836
|
C | CAAAAAAA others(12): Show |
3 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003 | 3 | HG01243.hp2 HG01884.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.502-4415_502-4414i others(21): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2620836 | |||||
| chr4:2620836
|
C | CAAAAAAA others(13): Show |
1 | a0001c0002t0001g0240 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.502-4415_502-4414i others(22): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2620836 | |||||
| chr4:2620836
|
CA | C | 159 | a0001c0001t0001g0004a0001c0001t0001g0122a0001c0001t0001g0123others(156): Show | 159 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.502-4404delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2620836 | |||||
| chr4:2621012
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-4250G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2621012 | ||||||
| chr4:2621018
|
C | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0142others(78): Show | 81 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.502-4244C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2621018 | ||||||
| chr4:2621089
|
G | A | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.502-4173G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2621089 | ||||||
| chr4:2621118
|
T | G | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.502-4144T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2621118 | ||||||
| chr4:2621632
|
C | T | 33 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(30): Show | 33 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.502-3630C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2621632 | ||||||
| chr4:2622121
|
G | T | 1 | a0001c0002t0001g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.502-3141G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2622121 | ||||||
| chr4:2622171
|
T | C | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.502-3091T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2622171 | ||||||
| chr4:2622257
|
C | CA | 45 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0142others(42): Show | 45 | HG00408.hp1 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.502-2979dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2622257 | |||||
| chr4:2622257
|
C | CAA | 23 | a0001c0001t0001g0158a0001c0001t0001g0194a0001c0001t0001g0220others(20): Show | 23 | HG00642.hp1 HG00741.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.502-2980_502-2979d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2622257 | |||||
| chr4:2622257
|
C | CAAA | 8 | a0001c0002t0001g0240a0001c0002t0003g0119a0001c0002t0003g0120others(5): Show | 8 | HG02055.hp2 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.502-2981_502-2979d others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2622257 | |||||
| chr4:2622257
|
C | CAAAAAAA others(3): Show |
2 | a0003c0003t0001g0233a0003c0003t0001g0238 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.502-2988_502-2979d others(12): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2622257 | |||||
| chr4:2622257
|
C | CAAAAAAA others(4): Show |
1 | a0003c0003t0001g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.502-2989_502-2979d others(13): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2622257 | |||||
| chr4:2622257
|
C | CAAAAAAA others(11): Show |
1 | a0003c0003t0001g0236 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.502-2996_502-2979d others(20): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2622257 | |||||
| chr4:2622257
|
CA | C | 90 | a0001c0001t0001g0145a0001c0001t0001g0157a0001c0001t0001g0168others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.502-2979delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2622257 | |||||
| chr4:2622257
|
CAAAAAA | C | 6 | a0001c0001t0002g0021a0006c0008t0001g0125a0006c0008t0001g0126others(3): Show | 6 | HG01106.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.502-2984_502-2979d others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2622257 | |||||
| chr4:2622257
|
CAAAAAAA others(3): Show |
C | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.502-2988_502-2979d others(12): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2622257 | |||||
| chr4:2622282
|
A | C | 1 | a0001c0001t0001g0305 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.502-2980A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2622282 | ||||||
| chr4:2622319
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.502-2943C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2622319 | ||||||
| chr4:2622493
|
GCCTGTGG others(2): Show |
G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-2767_502-2759d others(11): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2622493 | |||||
| chr4:2622735
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.502-2527C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2622735 | ||||||
| chr4:2622753
|
G | C | 5 | a0006c0008t0001g0121a0006c0008t0001g0126a0006c0008t0001g0127others(2): Show | 5 | HG02818.hp1 HG02895.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.502-2509G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2622753 | ||||||
| chr4:2622884
|
C | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.502-2378C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2622884 | ||||||
| chr4:2622890
|
C | T | 3 | a0001c0001t0001g0263a0001c0001t0001g0290a0002c0006t0001g0287 | 3 | HG00741.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.502-2372C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2622890 | ||||||
| chr4:2623323
|
C | G | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.502-1939C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2623323 | ||||||
| chr4:2623613
|
T | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.502-1649T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2623613 | ||||||
| chr4:2623627
|
G | T | 76 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.502-1635G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2623627 | ||||||
| chr4:2623752
|
G | T | 5 | a0001c0001t0001g0255a0001c0001t0001g0259a0001c0001t0001g0282others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.502-1510G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2623752 | ||||||
| chr4:2623790
|
G | A | 1 | a0003c0003t0011g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.502-1472G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2623790 | ||||||
| chr4:2623815
|
T | C | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-1447T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2623815 | ||||||
| chr4:2623898
|
T | C | 249 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.502-1364T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2623898 | ||||||
| chr4:2623902
|
A | G | 1 | a0006c0008t0001g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.502-1360A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2623902 | ||||||
| chr4:2623962
|
TCACCCTG others(4): Show |
T | 3 | a0001c0001t0001g0152a0001c0001t0001g0231a0001c0001t0001g0232 | 3 | HG02647.hp1 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.502-1293_502-1283d others(13): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2623962 | |||||
| chr4:2624013
|
C | G | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.502-1249C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2624013 | ||||||
| chr4:2624082
|
C | T | 1 | a0001c0001t0002g0099 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.502-1180C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2624082 | ||||||
| chr4:2624161
|
C | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.502-1101C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2624161 | ||||||
| chr4:2624183
|
C | CT | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.502-1068dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr4 | 2624183 | |||||
| chr4:2624381
|
T | C | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.502-881T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2624381 | ||||||
| chr4:2624424
|
G | A | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.502-838G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2624424 | ||||||
| chr4:2624433
|
T | C | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.502-829T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2624433 | ||||||
| chr4:2624440
|
G | A | 1 | a0001c0001t0003g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.502-822G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2624440 | ||||||
| chr4:2624711
|
A | T | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.502-551A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2624711 | ||||||
| chr4:2624810
|
G | A | 1 | a0002c0011t0003g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.502-452G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2624810 | ||||||
| chr4:2624842
|
G | A | 101 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.502-420G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2624842 | ||||||
| chr4:2624845
|
T | A | 5 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(2): Show | 5 | HG01891.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-417T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2624845 | ||||||
| chr4:2624868
|
G | C | 3 | a0001c0001t0001g0152a0001c0001t0001g0231a0001c0001t0001g0232 | 3 | HG02647.hp1 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.502-394G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2624868 | ||||||
| chr4:2624884
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.502-378A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2624884 | ||||||
| chr4:2624907
|
G | T | 1 | a0001c0001t0001g0294 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.502-355G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2624907 | ||||||
| chr4:2625070
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.502-192C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 2/20 | chr4 | 2625070 | ||||||
| chr4:2625434
|
C | T | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.635+39C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | chr4 | 2625434 | ||||||
| chr4:2625436
|
A | G | 3 | a0001c0001t0001g0152a0001c0001t0001g0231a0001c0001t0001g0232 | 3 | HG02647.hp1 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.635+41A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | chr4 | 2625436 | ||||||
| chr4:2625472
|
A | T | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.635+77A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | chr4 | 2625472 | ||||||
| chr4:2625519
|
C | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0040a0001c0001t0002g0047 | 3 | NA18967.hp1 NA19007.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.635+124C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | chr4 | 2625519 | ||||||
| chr4:2625605
|
A | AAGG | 12 | a0001c0016t0001g0308a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.635+213_635+215dup others(3): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr4 | 2625605 | |||||
| chr4:2625613
|
C | A | 1 | a0001c0001t0002g0030 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.635+218C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | chr4 | 2625613 | ||||||
| chr4:2625640
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.635+245C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | chr4 | 2625640 | ||||||
| chr4:2625719
|
C | CT | 21 | a0001c0001t0001g0123a0001c0001t0001g0142a0001c0001t0001g0145others(18): Show | 21 | HG00438.hp1 HG00673.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.635+349dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr4 | 2625719 | |||||
| chr4:2625719
|
CT | C | 61 | a0001c0001t0001g0065a0001c0001t0001g0157a0001c0001t0001g0168others(58): Show | 61 | HG00408.hp1 HG00609.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.635+349delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr4 | 2625719 | |||||
| chr4:2625719
|
CTT | C | 111 | a0001c0001t0001g0133a0001c0001t0002g0006a0001c0001t0002g0008others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.635+348_635+349del others(2): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr4 | 2625719 | |||||
| chr4:2625854
|
T | C | 1 | a0001c0001t0001g0212 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.635+459T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | chr4 | 2625854 | ||||||
| chr4:2625855
|
C | A | 1 | a0005c0005t0004g0141 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.635+460C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | chr4 | 2625855 | ||||||
| chr4:2625870
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.635+475C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | chr4 | 2625870 | ||||||
| chr4:2625871
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.635+476G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | chr4 | 2625871 | ||||||
| chr4:2625970
|
C | T | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.636-440C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | chr4 | 2625970 | ||||||
| chr4:2625971
|
G | A | 100 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.636-439G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | chr4 | 2625971 | ||||||
| chr4:2625978
|
C | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0273 | 2 | HG00733.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.636-432C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | chr4 | 2625978 | ||||||
| chr4:2626072
|
A | G | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.636-338A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | chr4 | 2626072 | ||||||
| chr4:2626118
|
A | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.636-292A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | chr4 | 2626118 | ||||||
| chr4:2626354
|
G | A | 1 | a0001c0001t0002g0064 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.636-56G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 3/20 | chr4 | 2626354 | ||||||
| chr4:2626642
|
C | A | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.803+65C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2626642 | ||||||
| chr4:2626845
|
A | G | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.803+268A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2626845 | ||||||
| chr4:2626847
|
T | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.803+270T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2626847 | ||||||
| chr4:2626938
|
C | T | 3 | a0001c0001t0001g0253a0009c0010t0014g0228a0009c0010t0015g0229 | 3 | HG01167.hp1 HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.803+361C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2626938 | ||||||
| chr4:2627127
|
T | A | 102 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.803+550T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2627127 | ||||||
| chr4:2627159
|
C | CT | 142 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(139): Show | 142 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.803+601dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2627159 | |||||
| chr4:2627159
|
CT | C | 10 | a0001c0001t0001g0142a0001c0001t0001g0177a0001c0001t0001g0225others(7): Show | 10 | HG01099.hp2 HG02145.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.803+601delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2627159 | |||||
| chr4:2627193
|
C | G | 4 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+616C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2627193 | ||||||
| chr4:2627239
|
C | T | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.803+662C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2627239 | ||||||
| chr4:2627357
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.803+780C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2627357 | ||||||
| chr4:2627376
|
G | C | 1 | a0001c0001t0002g0092 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.803+799G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2627376 | ||||||
| chr4:2627386
|
T | A | 102 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.803+809T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2627386 | ||||||
| chr4:2627387
|
AATCCACC others(134): Show |
A | 102 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.803+811_803+951del | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2627387 | ||||||
| chr4:2627436
|
A | C | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.803+859A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2627436 | ||||||
| chr4:2627531
|
T | G | 102 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.803+954T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2627531 | ||||||
| chr4:2627532
|
T | G | 102 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.803+955T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2627532 | ||||||
| chr4:2627575
|
C | CT | 18 | a0001c0001t0001g0123a0001c0001t0001g0159a0001c0001t0001g0162others(15): Show | 18 | HG00741.hp2 HG01175.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.803+1018dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2627575 | |||||
| chr4:2627575
|
C | CTT | 7 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(4): Show | 7 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.803+1017_803+1018d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2627575 | |||||
| chr4:2627575
|
C | CTTTTTT | 7 | a0004c0004t0001g0318a0004c0004t0001g0322a0004c0004t0001g0325others(4): Show | 7 | HG02257.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.803+1013_803+1018d others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2627575 | |||||
| chr4:2627575
|
CT | C | 112 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0152others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.803+1018delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2627575 | |||||
| chr4:2627610
|
C | G | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.803+1033C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2627610 | ||||||
| chr4:2627627
|
A | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.803+1050A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2627627 | ||||||
| chr4:2627744
|
A | AT | 9 | a0001c0001t0001g0241a0001c0001t0002g0041a0001c0001t0002g0047others(6): Show | 9 | HG01891.hp2 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.803+1183dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2627744 | |||||
| chr4:2627773
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.803+1196C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2627773 | ||||||
| chr4:2627886
|
G | A | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.803+1309G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2627886 | ||||||
| chr4:2627963
|
T | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.803+1386T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2627963 | ||||||
| chr4:2627985
|
G | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.803+1408G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2627985 | ||||||
| chr4:2628043
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.803+1466C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2628043 | ||||||
| chr4:2628044
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.803+1467G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2628044 | ||||||
| chr4:2628183
|
C | T | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.803+1606C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2628183 | ||||||
| chr4:2628184
|
G | A | 13 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.803+1607G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2628184 | ||||||
| chr4:2628378
|
G | A | 10 | a0001c0001t0001g0122a0002c0012t0004g0328a0005c0005t0004g0128others(7): Show | 10 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.803+1801G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2628378 | ||||||
| chr4:2628489
|
T | C | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.803+1912T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2628489 | ||||||
| chr4:2628559
|
C | T | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.803+1982C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2628559 | ||||||
| chr4:2628738
|
A | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.803+2161A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2628738 | ||||||
| chr4:2628747
|
C | T | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.803+2170C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2628747 | ||||||
| chr4:2628754
|
G | A | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | HG02004.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.803+2177G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2628754 | ||||||
| chr4:2628851
|
CTCTT | C | 100 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.804-2082_804-2079d others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2628851 | |||||
| chr4:2628853
|
C | CT | 23 | a0001c0001t0001g0122a0001c0001t0001g0262a0002c0012t0004g0328others(20): Show | 23 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.804-2065dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2628853 | |||||
| chr4:2628853
|
CT | C | 9 | a0001c0001t0001g0207a0001c0001t0001g0218a0001c0001t0001g0225others(6): Show | 9 | HG00280.hp1 HG00558.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-2065delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2628853 | |||||
| chr4:2628855
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.804-2080T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2628855 | ||||||
| chr4:2628887
|
C | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.804-2048C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2628887 | ||||||
| chr4:2628939
|
G | A | 1 | a0012c0020t0004g0192 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.804-1996G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2628939 | ||||||
| chr4:2628972
|
C | G | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.804-1963C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2628972 | ||||||
| chr4:2628976
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.804-1959G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2628976 | ||||||
| chr4:2628997
|
C | T | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.804-1938C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2628997 | ||||||
| chr4:2629075
|
A | G | 1 | a0001c0001t0006g0016 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.804-1860A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2629075 | ||||||
| chr4:2629219
|
C | CA | 9 | a0001c0001t0001g0152a0001c0001t0001g0262a0001c0001t0002g0008others(6): Show | 9 | HG01106.hp1 HG02145.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.804-1704dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2629219 | |||||
| chr4:2629219
|
C | CAA | 95 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.804-1705_804-1704d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2629219 | |||||
| chr4:2629236
|
T | C | 29 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(26): Show | 29 | HG00609.hp2 HG01243.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.804-1699T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2629236 | ||||||
| chr4:2629282
|
G | A | 72 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0248others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.804-1653G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2629282 | ||||||
| chr4:2629702
|
G | C | 15 | a0001c0001t0001g0122a0001c0001t0001g0152a0001c0001t0001g0231others(12): Show | 15 | HG00408.hp1 HG01074.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.804-1233G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2629702 | ||||||
| chr4:2629727
|
C | T | 1 | a0005c0005t0004g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.804-1208C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2629727 | ||||||
| chr4:2629904
|
G | T | 7 | a0003c0003t0004g0155a0003c0003t0005g0164a0003c0003t0005g0187others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.804-1031G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2629904 | ||||||
| chr4:2629908
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.804-1027G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2629908 | ||||||
| chr4:2629928
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.804-1007C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2629928 | ||||||
| chr4:2629930
|
G | A | 6 | a0001c0001t0002g0063a0001c0002t0001g0001a0001c0002t0001g0002others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.804-1005G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2629930 | ||||||
| chr4:2629939
|
T | C | 1 | a0001c0001t0012g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.804-996T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2629939 | ||||||
| chr4:2629946
|
C | G | 1 | a0001c0001t0001g0297 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.804-989C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2629946 | ||||||
| chr4:2629947
|
A | G | 10 | a0001c0001t0001g0122a0001c0021t0003g0143a0002c0012t0004g0328others(7): Show | 10 | HG00408.hp1 HG01975.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.804-988A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2629947 | ||||||
| chr4:2629948
|
T | C | 1 | a0015c0015t0002g0028 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.804-987T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2629948 | ||||||
| chr4:2630101
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.804-834C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2630101 | ||||||
| chr4:2630131
|
C | CA | 14 | a0001c0001t0001g0122a0001c0001t0001g0209a0001c0001t0001g0264others(11): Show | 14 | HG00673.hp1 HG02015.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.804-788dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2630131 | |||||
| chr4:2630131
|
CA | C | 34 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(31): Show | 34 | HG00609.hp2 HG01243.hp2 HG01516.hp1 others(31): Show |
intron_variant | MODIFIER | c.804-788delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2630131 | |||||
| chr4:2630168
|
T | G | 77 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.804-767T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2630168 | ||||||
| chr4:2630224
|
AT | A | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.804-709delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2630224 | |||||
| chr4:2630233
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.804-702G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2630233 | ||||||
| chr4:2630255
|
A | AT | 13 | a0001c0001t0002g0014a0004c0004t0001g0318a0004c0004t0001g0321others(10): Show | 13 | HG00140.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.804-670dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2630255 | |||||
| chr4:2630330
|
T | TA | 100 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.804-595dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2630330 | |||||
| chr4:2630330
|
TA | T | 20 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(17): Show | 20 | HG00609.hp2 HG01891.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.804-595delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2630330 | |||||
| chr4:2630330
|
TAA | T | 34 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(31): Show | 34 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.804-596_804-595del others(2): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 2630330 | |||||
| chr4:2630491
|
T | C | 4 | a0004c0004t0001g0321a0004c0004t0003g0317a0004c0004t0003g0319others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.804-444T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2630491 | ||||||
| chr4:2630574
|
T | G | 2 | a0001c0001t0001g0150a0001c0001t0010g0149 | 2 | HG00639.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.804-361T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2630574 | ||||||
| chr4:2630703
|
C | T | 12 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.804-232C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2630703 | ||||||
| chr4:2630745
|
A | C | 1 | a0001c0001t0001g0246 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.804-190A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2630745 | ||||||
| chr4:2630802
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.804-133G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2630802 | ||||||
| chr4:2630891
|
T | G | 2 | a0001c0001t0001g0150a0001c0001t0010g0149 | 2 | HG00639.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.804-44T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 4/20 | chr4 | 2630891 | ||||||
| chr4:2631257
|
A | C | 1 | a0002c0006t0002g0105 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1038+88A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2631257 | ||||||
| chr4:2631261
|
C | T | 2 | a0002c0006t0002g0105a0005c0005t0004g0136 | 2 | HG01975.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1038+92C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2631261 | ||||||
| chr4:2631383
|
A | C | 9 | a0001c0001t0001g0251a0001c0001t0001g0258a0001c0001t0001g0278others(6): Show | 9 | HG01099.hp2 HG01106.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.1038+214A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2631383 | ||||||
| chr4:2631491
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1038+322G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2631491 | ||||||
| chr4:2631640
|
C | T | 1 | a0001c0001t0002g0009 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1038+471C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2631640 | ||||||
| chr4:2631750
|
C | G | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1038+581C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2631750 | ||||||
| chr4:2631854
|
C | A | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1038+685C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2631854 | ||||||
| chr4:2632056
|
C | CT | 29 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(26): Show | 29 | HG00609.hp2 HG01243.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.1038+888dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | 2632056 | |||||
| chr4:2632068
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1038+899G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2632068 | ||||||
| chr4:2632076
|
C | T | 2 | a0004c0004t0001g0323a0004c0004t0001g0327 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1038+907C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2632076 | ||||||
| chr4:2632103
|
A | T | 1 | a0002c0012t0004g0328 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1038+934A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2632103 | ||||||
| chr4:2632168
|
GTTTTGGG others(4): Show |
G | 1 | a0001c0001t0002g0006 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1038+1002_1038+101 others(15): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | 2632168 | |||||
| chr4:2632404
|
A | C | 31 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(28): Show | 31 | HG00609.hp2 HG01243.hp2 HG01516.hp1 others(28): Show |
intron_variant | MODIFIER | c.1038+1235A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2632404 | ||||||
| chr4:2632808
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1038+1639C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2632808 | ||||||
| chr4:2632819
|
G | C | 1 | a0005c0005t0002g0138 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1038+1650G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2632819 | ||||||
| chr4:2632882
|
C | T | 66 | a0001c0001t0001g0122a0001c0002t0001g0001a0001c0002t0001g0002others(63): Show | 66 | HG00408.hp1 HG00609.hp2 HG01074.hp1 others(63): Show |
intron_variant | MODIFIER | c.1038+1713C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2632882 | ||||||
| chr4:2633138
|
C | T | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1038+1969C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2633138 | ||||||
| chr4:2633164
|
G | A | 3 | a0001c0001t0001g0299a0001c0001t0007g0129a0001c0001t0007g0137 | 3 | HG01167.hp2 HG02083.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1038+1995G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2633164 | ||||||
| chr4:2633175
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1038+2006A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2633175 | ||||||
| chr4:2633301
|
A | C | 1 | a0001c0001t0001g0314 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1038+2132A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2633301 | ||||||
| chr4:2633342
|
T | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1038+2173T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2633342 | ||||||
| chr4:2633462
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1038+2293C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2633462 | ||||||
| chr4:2633721
|
G | A | 1 | a0001c0018t0001g0260 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1038+2552G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2633721 | ||||||
| chr4:2633791
|
G | A | 31 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(28): Show | 31 | HG00609.hp2 HG01243.hp2 HG01516.hp1 others(28): Show |
intron_variant | MODIFIER | c.1038+2622G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2633791 | ||||||
| chr4:2633834
|
A | G | 1 | a0001c0018t0001g0260 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1038+2665A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2633834 | ||||||
| chr4:2633845
|
A | G | 3 | a0001c0001t0001g0298a0001c0001t0001g0314a0001c0001t0001g0315 | 3 | HG02015.hp1 HG02056.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1038+2676A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2633845 | ||||||
| chr4:2633853
|
G | A | 1 | a0001c0001t0012g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1038+2684G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2633853 | ||||||
| chr4:2633903
|
A | G | 31 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(28): Show | 31 | HG00609.hp2 HG01243.hp2 HG01516.hp1 others(28): Show |
intron_variant | MODIFIER | c.1038+2734A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2633903 | ||||||
| chr4:2633911
|
T | C | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1038+2742T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2633911 | ||||||
| chr4:2633979
|
T | C | 13 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1038+2810T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2633979 | ||||||
| chr4:2634038
|
A | T | 1 | a0001c0001t0001g0255 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1038+2869A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2634038 | ||||||
| chr4:2634137
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1038+2968G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2634137 | ||||||
| chr4:2634167
|
T | G | 1 | a0001c0025t0001g0224 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1038+2998T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2634167 | ||||||
| chr4:2634254
|
G | A | 3 | a0004c0004t0001g0318a0004c0004t0001g0322a0004c0017t0001g0324 | 3 | HG02258.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1038+3085G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2634254 | ||||||
| chr4:2634301
|
T | C | 31 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(28): Show | 31 | HG00609.hp2 HG01243.hp2 HG01516.hp1 others(28): Show |
intron_variant | MODIFIER | c.1038+3132T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2634301 | ||||||
| chr4:2634315
|
A | G | 42 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(39): Show | 42 | HG00609.hp2 HG01243.hp2 HG01516.hp1 others(39): Show |
intron_variant | MODIFIER | c.1038+3146A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2634315 | ||||||
| chr4:2634406
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1038+3237A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2634406 | ||||||
| chr4:2634715
|
C | T | 1 | a0001c0001t0003g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1038+3546C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2634715 | ||||||
| chr4:2634951
|
T | C | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1038+3782T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2634951 | ||||||
| chr4:2635077
|
T | A | 5 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(2): Show | 5 | HG01891.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1038+3908T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2635077 | ||||||
| chr4:2635079
|
C | A | 13 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(10): Show | 13 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1038+3910C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2635079 | ||||||
| chr4:2635154
|
A | G | 11 | a0001c0001t0001g0122a0002c0012t0004g0328a0005c0005t0002g0138others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.1038+3985A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2635154 | ||||||
| chr4:2635631
|
C | G | 1 | a0001c0001t0001g0298 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1039-4104C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2635631 | ||||||
| chr4:2635635
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1039-4100C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2635635 | ||||||
| chr4:2635824
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1039-3911C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2635824 | ||||||
| chr4:2635833
|
C | T | 100 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.1039-3902C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2635833 | ||||||
| chr4:2636000
|
A | ATTTTT | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1039-3726_1039-372 others(9): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | 2636000 | |||||
| chr4:2636000
|
A | ATTTTTT | 7 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(4): Show | 7 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-3727_1039-372 others(10): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | 2636000 | |||||
| chr4:2636000
|
AT | A | 13 | a0001c0001t0002g0094a0003c0003t0001g0233a0003c0003t0001g0234others(10): Show | 13 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1039-3722delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | 2636000 | |||||
| chr4:2636343
|
G | C | 12 | a0001c0001t0001g0122a0001c0021t0003g0143a0002c0012t0004g0328others(9): Show | 12 | HG00408.hp1 HG01074.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1039-3392G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2636343 | ||||||
| chr4:2636593
|
A | G | 1 | a0001c0001t0002g0071 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1039-3142A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2636593 | ||||||
| chr4:2636652
|
T | C | 42 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(39): Show | 42 | HG00609.hp2 HG01243.hp2 HG01516.hp1 others(39): Show |
intron_variant | MODIFIER | c.1039-3083T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2636652 | ||||||
| chr4:2636740
|
C | A | 1 | a0001c0001t0001g0307 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1039-2995C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2636740 | ||||||
| chr4:2636954
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1039-2781C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2636954 | ||||||
| chr4:2636960
|
G | GT | 5 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(2): Show | 5 | HG01891.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1039-2772dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | 2636960 | |||||
| chr4:2637138
|
G | A | 12 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1039-2597G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2637138 | ||||||
| chr4:2637259
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1039-2476G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2637259 | ||||||
| chr4:2637328
|
G | A | 1 | a0005c0005t0004g0128 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1039-2407G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2637328 | ||||||
| chr4:2637332
|
A | G | 1 | a0001c0001t0002g0094 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1039-2403A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2637332 | ||||||
| chr4:2637379
|
A | C | 103 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1039-2356A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2637379 | ||||||
| chr4:2637490
|
G | A | 13 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(10): Show | 13 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1039-2245G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2637490 | ||||||
| chr4:2637519
|
T | A | 14 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(11): Show | 14 | HG01167.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1039-2216T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2637519 | ||||||
| chr4:2637713
|
C | G | 75 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.1039-2022C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2637713 | ||||||
| chr4:2638086
|
G | A | 2 | a0001c0001t0002g0330a0002c0006t0002g0046 | 2 | HG03927.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1039-1649G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2638086 | ||||||
| chr4:2638174
|
A | C | 1 | a0001c0001t0001g0313 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1039-1561A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2638174 | ||||||
| chr4:2638174
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1039-1561A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2638174 | ||||||
| chr4:2638230
|
A | T | 1 | a0007c0007t0001g0110 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1039-1505A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2638230 | ||||||
| chr4:2638327
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1039-1408G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2638327 | ||||||
| chr4:2638420
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1039-1315C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2638420 | ||||||
| chr4:2638628
|
A | ACAGAGCT others(4): Show |
1 | a0001c0001t0001g0261 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1039-1105_1039-109 others(15): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | 2638628 | |||||
| chr4:2638679
|
G | A | 1 | a0001c0002t0009g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1039-1056G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2638679 | ||||||
| chr4:2638717
|
CAATCATT others(2): Show |
C | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1039-1005_1039-997 others(12): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | 2638717 | |||||
| chr4:2638735
|
T | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1039-1000T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2638735 | ||||||
| chr4:2638773
|
T | C | 248 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1039-962T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2638773 | ||||||
| chr4:2639164
|
A | T | 1 | a0006c0008t0001g0124 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1039-571A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2639164 | ||||||
| chr4:2639172
|
G | A | 1 | a0001c0001t0004g0208 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1039-563G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2639172 | ||||||
| chr4:2639405
|
T | C | 12 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1039-330T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2639405 | ||||||
| chr4:2639509
|
G | C | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1039-226G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 5/20 | chr4 | 2639509 | ||||||
| chr4:2639879
|
A | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1163+20A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2639879 | ||||||
| chr4:2639959
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1163+100C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2639959 | ||||||
| chr4:2640050
|
TAA | T | 101 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1163+192_1163+193d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2640050 | ||||||
| chr4:2640246
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1163+387C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2640246 | ||||||
| chr4:2640276
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1163+417C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2640276 | ||||||
| chr4:2640421
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1163+562G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2640421 | ||||||
| chr4:2640610
|
A | G | 1 | a0002c0006t0001g0268 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1163+751A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2640610 | ||||||
| chr4:2640701
|
C | T | 11 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(8): Show | 11 | HG01891.hp2 HG02257.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1163+842C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2640701 | ||||||
| chr4:2640727
|
G | A | 1 | a0001c0001t0002g0015 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1163+868G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2640727 | ||||||
| chr4:2640753
|
T | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1163+894T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2640753 | ||||||
| chr4:2640832
|
G | T | 1 | a0002c0011t0003g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1163+973G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2640832 | ||||||
| chr4:2640864
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1163+1005C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2640864 | ||||||
| chr4:2640866
|
G | T | 1 | a0001c0001t0003g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1163+1007G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2640866 | ||||||
| chr4:2641064
|
A | G | 97 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1163+1205A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2641064 | ||||||
| chr4:2641108
|
T | C | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1163+1249T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2641108 | ||||||
| chr4:2641278
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1163+1419G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2641278 | ||||||
| chr4:2641311
|
T | G | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1163+1452T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2641311 | ||||||
| chr4:2641386
|
C | T | 1 | a0002c0006t0002g0102 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1163+1527C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2641386 | ||||||
| chr4:2641523
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1163+1664C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2641523 | ||||||
| chr4:2641524
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1163+1665G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2641524 | ||||||
| chr4:2641950
|
A | C | 2 | a0004c0004t0001g0323a0004c0004t0001g0327 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1163+2091A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2641950 | ||||||
| chr4:2641953
|
A | AGGGCCAG others(47): Show |
2 | a0001c0001t0001g0150a0001c0001t0010g0149 | 2 | HG00639.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1163+2106_1163+215 others(58): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2641953 | |||||
| chr4:2642007
|
C | T | 1 | a0001c0002t0013g0117 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1163+2148C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642007 | ||||||
| chr4:2642066
|
A | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1163+2207A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642066 | ||||||
| chr4:2642102
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1163+2243A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642102 | ||||||
| chr4:2642117
|
C | T | 9 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(6): Show | 9 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1163+2258C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642117 | ||||||
| chr4:2642134
|
C | CA | 36 | a0001c0001t0001g0122a0001c0001t0001g0144a0001c0001t0001g0146others(33): Show | 36 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.1163+2295dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2642134 | |||||
| chr4:2642134
|
C | CAAAA | 10 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1163+2292_1163+229 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2642134 | |||||
| chr4:2642134
|
CA | C | 13 | a0001c0001t0001g0214a0001c0001t0001g0243a0001c0001t0001g0267others(10): Show | 13 | HG00733.hp2 HG01256.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.1163+2295delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2642134 | |||||
| chr4:2642134
|
CAA | C | 79 | a0001c0001t0001g0152a0001c0001t0001g0241a0001c0001t0001g0244others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1163+2294_1163+229 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2642134 | |||||
| chr4:2642134
|
CAAAAAA | C | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1163+2290_1163+229 others(10): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2642134 | |||||
| chr4:2642173
|
G | A | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1163+2314G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642173 | ||||||
| chr4:2642175
|
G | A | 4 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0304others(1): Show | 4 | HG02004.hp2 HG02630.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163+2316G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642175 | ||||||
| chr4:2642177
|
A | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1163+2318A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642177 | ||||||
| chr4:2642190
|
G | C | 9 | a0001c0002t0016g0023a0007c0007t0001g0110a0007c0007t0001g0115others(6): Show | 9 | HG01891.hp1 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1163+2331G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642190 | ||||||
| chr4:2642196
|
C | T | 1 | a0002c0011t0003g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1163+2337C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642196 | ||||||
| chr4:2642304
|
A | G | 2 | a0004c0004t0001g0323a0004c0004t0001g0327 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1163+2445A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642304 | ||||||
| chr4:2642338
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1163+2479C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642338 | ||||||
| chr4:2642566
|
G | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0309a0001c0001t0001g0311 | 3 | NA18940.hp1 NA18959.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1163+2707G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642566 | ||||||
| chr4:2642584
|
T | C | 172 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(169): Show | 172 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1163+2725T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642584 | ||||||
| chr4:2642635
|
TA | T | 77 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1163+2785delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2642635 | |||||
| chr4:2642718
|
C | G | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1163+2859C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642718 | ||||||
| chr4:2642732
|
C | CT | 23 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(20): Show | 23 | HG01167.hp2 HG02056.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1163+2890dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2642732 | |||||
| chr4:2642732
|
CT | C | 11 | a0001c0001t0002g0015a0003c0003t0001g0238a0006c0008t0001g0005others(8): Show | 11 | HG00609.hp2 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1163+2890delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2642732 | |||||
| chr4:2642772
|
G | A | 102 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1163+2913G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642772 | ||||||
| chr4:2642795
|
A | G | 1 | a0005c0005t0004g0135 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1163+2936A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642795 | ||||||
| chr4:2642828
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1163+2969G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642828 | ||||||
| chr4:2642989
|
A | G | 75 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.1163+3130A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2642989 | ||||||
| chr4:2643074
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1163+3215T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2643074 | ||||||
| chr4:2643161
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1163+3302C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2643161 | ||||||
| chr4:2643234
|
T | A | 102 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1163+3375T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2643234 | ||||||
| chr4:2643286
|
T | C | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1164-3399T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2643286 | ||||||
| chr4:2643347
|
T | TA | 40 | a0001c0001t0001g0122a0001c0002t0001g0001a0001c0002t0001g0002others(37): Show | 40 | HG00408.hp1 HG00609.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.1164-3337dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2643347 | |||||
| chr4:2643395
|
T | A | 245 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1164-3290T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2643395 | ||||||
| chr4:2643547
|
A | AC | 263 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1164-3136dupC | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2643547 | |||||
| chr4:2643614
|
G | C | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1164-3071G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2643614 | ||||||
| chr4:2643653
|
A | T | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1164-3032A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2643653 | ||||||
| chr4:2643719
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1164-2966C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2643719 | ||||||
| chr4:2643751
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1164-2934C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2643751 | ||||||
| chr4:2643755
|
G | T | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1164-2930G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2643755 | ||||||
| chr4:2643845
|
T | C | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1164-2840T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2643845 | ||||||
| chr4:2643851
|
A | G | 1 | a0003c0003t0011g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1164-2834A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2643851 | ||||||
| chr4:2643905
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0286 | 2 | HG00140.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.1164-2780T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2643905 | ||||||
| chr4:2644227
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1164-2458C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2644227 | ||||||
| chr4:2644251
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1164-2434A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2644251 | ||||||
| chr4:2644360
|
G | T | 1 | a0001c0001t0002g0064 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1164-2325G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2644360 | ||||||
| chr4:2644490
|
T | A | 67 | a0001c0001t0001g0122a0001c0002t0001g0001a0001c0002t0001g0002others(64): Show | 67 | HG00408.hp1 HG00609.hp2 HG01074.hp1 others(64): Show |
intron_variant | MODIFIER | c.1164-2195T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2644490 | ||||||
| chr4:2644654
|
CCT | C | 9 | a0001c0002t0016g0023a0007c0007t0001g0110a0007c0007t0001g0115others(6): Show | 9 | HG01891.hp1 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1164-2028_1164-202 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2644654 | |||||
| chr4:2644708
|
G | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0170a0001c0001t0001g0175 | 3 | HG02258.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1164-1977G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2644708 | ||||||
| chr4:2644716
|
A | G | 53 | a0001c0001t0001g0122a0001c0002t0001g0001a0001c0002t0001g0002others(50): Show | 53 | HG00408.hp1 HG00609.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.1164-1969A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2644716 | ||||||
| chr4:2644873
|
T | C | 11 | a0001c0001t0001g0122a0002c0012t0004g0328a0005c0005t0002g0138others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.1164-1812T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2644873 | ||||||
| chr4:2645034
|
A | ATG | 12 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(9): Show | 12 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1164-1624_1164-162 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2645034 | |||||
| chr4:2645034
|
ATG | A | 136 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1164-1624_1164-162 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2645034 | |||||
| chr4:2645034
|
ATGTG | A | 95 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(92): Show | 95 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.1164-1626_1164-162 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2645034 | |||||
| chr4:2645198
|
A | G | 4 | a0004c0004t0001g0321a0004c0004t0003g0317a0004c0004t0003g0319others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164-1487A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2645198 | ||||||
| chr4:2645303
|
A | G | 1 | a0001c0001t0008g0249 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1164-1382A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2645303 | ||||||
| chr4:2645404
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1164-1281C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2645404 | ||||||
| chr4:2645431
|
G | A | 1 | a0002c0012t0004g0328 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1164-1254G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2645431 | ||||||
| chr4:2645548
|
G | C | 13 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1164-1137G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2645548 | ||||||
| chr4:2645645
|
G | C | 21 | a0001c0001t0001g0122a0002c0012t0004g0328a0005c0005t0002g0138others(18): Show | 21 | HG00408.hp1 HG00609.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1164-1040G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2645645 | ||||||
| chr4:2645729
|
G | A | 13 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1164-956G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2645729 | ||||||
| chr4:2645817
|
G | C | 1 | a0001c0001t0001g0201 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1164-868G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2645817 | ||||||
| chr4:2645843
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1164-842C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2645843 | ||||||
| chr4:2645911
|
A | G | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1164-774A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2645911 | ||||||
| chr4:2646081
|
T | C | 21 | a0001c0001t0001g0122a0002c0012t0004g0328a0005c0005t0002g0138others(18): Show | 21 | HG00408.hp1 HG00609.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1164-604T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2646081 | ||||||
| chr4:2646159
|
C | CT | 16 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0153others(13): Show | 16 | HG00438.hp1 HG01256.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.1164-498dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2646159 | |||||
| chr4:2646159
|
CTTT | C | 15 | a0001c0001t0001g0122a0001c0001t0002g0009a0004c0004t0001g0321others(12): Show | 15 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.1164-500_1164-498d others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2646159 | |||||
| chr4:2646159
|
CTTTT | C | 23 | a0001c0001t0001g0246a0001c0001t0001g0262a0001c0001t0001g0264others(20): Show | 23 | HG00544.hp2 HG00673.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1164-501_1164-498d others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2646159 | |||||
| chr4:2646159
|
CTTTTT | C | 164 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1164-502_1164-498d others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2646159 | |||||
| chr4:2646159
|
CTTTTTT | C | 22 | a0001c0001t0001g0253a0001c0001t0001g0281a0001c0001t0001g0303others(19): Show | 22 | HG01070.hp1 HG01167.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1164-503_1164-498d others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2646159 | |||||
| chr4:2646159
|
CTTTTTTT | C | 9 | a0001c0002t0016g0023a0007c0007t0001g0110a0007c0007t0001g0115others(6): Show | 9 | HG01891.hp1 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1164-504_1164-498d others(9): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2646159 | |||||
| chr4:2646159
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0194 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1164-509_1164-498d others(14): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2646159 | |||||
| chr4:2646159
|
CTTTTTTT others(10): Show |
C | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1164-514_1164-498d others(19): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 2646159 | |||||
| chr4:2646200
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1164-485C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2646200 | ||||||
| chr4:2646377
|
G | A | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1164-308G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2646377 | ||||||
| chr4:2646382
|
T | C | 21 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(18): Show | 21 | HG00609.hp2 HG02145.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1164-303T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2646382 | ||||||
| chr4:2646493
|
C | T | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1164-192C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2646493 | ||||||
| chr4:2646511
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1164-174A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2646511 | ||||||
| chr4:2646521
|
G | A | 55 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(52): Show | 55 | HG00609.hp2 HG01243.hp2 HG01516.hp1 others(52): Show |
intron_variant | MODIFIER | c.1164-164G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2646521 | ||||||
| chr4:2646536
|
C | G | 10 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(7): Show | 10 | HG00609.hp2 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1164-149C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2646536 | ||||||
| chr4:2646665
|
C | A | 1 | a0001c0001t0001g0299 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1164-20C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 6/20 | chr4 | 2646665 | ||||||
| chr4:2646939
|
C | T | 2 | a0007c0007t0003g0106a0007c0007t0003g0107 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1311+107C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2646939 | ||||||
| chr4:2646948
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1311+116C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2646948 | ||||||
| chr4:2647091
|
G | T | 1 | a0003c0003t0004g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1311+259G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2647091 | ||||||
| chr4:2647153
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1311+321C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2647153 | ||||||
| chr4:2647286
|
C | T | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1311+454C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2647286 | ||||||
| chr4:2647313
|
G | A | 21 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(18): Show | 21 | HG00609.hp2 HG02145.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1311+481G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2647313 | ||||||
| chr4:2647335
|
A | G | 245 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1311+503A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2647335 | ||||||
| chr4:2647363
|
C | A | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1311+531C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2647363 | ||||||
| chr4:2647474
|
C | G | 3 | a0001c0001t0001g0262a0001c0001t0001g0285a0001c0016t0001g0308 | 3 | HG02109.hp2 HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1311+642C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2647474 | ||||||
| chr4:2647671
|
C | T | 1 | a0007c0007t0003g0108 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1311+839C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2647671 | ||||||
| chr4:2647694
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1311+862C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2647694 | ||||||
| chr4:2647694
|
C | T | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1311+862C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2647694 | ||||||
| chr4:2647731
|
A | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1311+899A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2647731 | ||||||
| chr4:2647827
|
T | A | 4 | a0001c0001t0002g0056a0001c0001t0002g0059a0001c0001t0002g0095others(1): Show | 4 | HG02015.hp2 HG02040.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1311+995T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2647827 | ||||||
| chr4:2648051
|
T | C | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1311+1219T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2648051 | ||||||
| chr4:2648834
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1311+2002G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2648834 | ||||||
| chr4:2648864
|
A | G | 1 | a0006c0008t0001g0005 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1311+2032A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2648864 | ||||||
| chr4:2648879
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1311+2047G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2648879 | ||||||
| chr4:2648938
|
C | T | 10 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(7): Show | 10 | HG00609.hp2 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1311+2106C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2648938 | ||||||
| chr4:2649221
|
A | C | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1311+2389A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2649221 | ||||||
| chr4:2649237
|
G | A | 1 | a0006c0008t0001g0121 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1311+2405G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2649237 | ||||||
| chr4:2649374
|
G | A | 3 | a0004c0004t0001g0323a0009c0010t0014g0228a0009c0010t0015g0229 | 3 | HG02145.hp1 HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1311+2542G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2649374 | ||||||
| chr4:2649374
|
G | C | 18 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(15): Show | 18 | HG00609.hp2 HG02257.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1311+2542G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2649374 | ||||||
| chr4:2649374
|
G | GA | 28 | a0001c0001t0001g0122a0001c0001t0001g0152a0001c0001t0001g0166others(25): Show | 28 | HG00408.hp1 HG00642.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1311+2559dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 2649374 | |||||
| chr4:2649525
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1311+2693A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2649525 | ||||||
| chr4:2649564
|
C | T | 13 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1311+2732C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2649564 | ||||||
| chr4:2649722
|
G | A | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1311+2890G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2649722 | ||||||
| chr4:2649747
|
C | T | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1311+2915C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2649747 | ||||||
| chr4:2649919
|
T | C | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1311+3087T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2649919 | ||||||
| chr4:2649949
|
C | A | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1311+3117C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2649949 | ||||||
| chr4:2650000
|
C | T | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1311+3168C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650000 | ||||||
| chr4:2650118
|
A | C | 13 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1311+3286A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650118 | ||||||
| chr4:2650144
|
G | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1311+3312G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650144 | ||||||
| chr4:2650257
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | NA18940.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1311+3425C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650257 | ||||||
| chr4:2650326
|
G | A | 1 | a0005c0005t0004g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1311+3494G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650326 | ||||||
| chr4:2650359
|
G | A | 2 | a0001c0001t0001g0284a0001c0001t0001g0291 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1311+3527G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650359 | ||||||
| chr4:2650428
|
G | A | 6 | a0001c0001t0002g0012a0001c0001t0002g0014a0001c0001t0002g0029others(3): Show | 6 | HG00140.hp1 HG01168.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1311+3596G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650428 | ||||||
| chr4:2650440
|
C | T | 2 | a0001c0001t0001g0307a0003c0003t0004g0155 | 2 | HG02523.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1311+3608C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650440 | ||||||
| chr4:2650451
|
C | T | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1311+3619C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650451 | ||||||
| chr4:2650452
|
G | A | 2 | a0001c0001t0001g0267a0001c0001t0001g0293 | 2 | NA18946.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1311+3620G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650452 | ||||||
| chr4:2650473
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1311+3641G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650473 | ||||||
| chr4:2650477
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1311+3645C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650477 | ||||||
| chr4:2650487
|
C | G | 2 | a0004c0004t0001g0323a0004c0004t0001g0327 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1311+3655C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650487 | ||||||
| chr4:2650535
|
G | T | 3 | a0001c0021t0003g0143a0009c0010t0014g0228a0009c0010t0015g0229 | 3 | HG02486.hp2 HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1311+3703G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650535 | ||||||
| chr4:2650718
|
A | G | 1 | a0002c0011t0003g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1311+3886A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650718 | ||||||
| chr4:2650765
|
T | C | 256 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1311+3933T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650765 | ||||||
| chr4:2650770
|
A | G | 1 | a0001c0001t0002g0064 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1311+3938A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650770 | ||||||
| chr4:2650836
|
G | A | 16 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0168others(13): Show | 16 | HG01167.hp2 HG02258.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1311+4004G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650836 | ||||||
| chr4:2650837
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1311+4005C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650837 | ||||||
| chr4:2650841
|
C | T | 12 | a0001c0002t0001g0113a0001c0002t0003g0116a0001c0002t0003g0119others(9): Show | 12 | HG01891.hp1 HG02717.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1311+4009C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650841 | ||||||
| chr4:2650869
|
T | A | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1311+4037T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2650869 | ||||||
| chr4:2651084
|
A | G | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1311+4252A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2651084 | ||||||
| chr4:2651147
|
A | C | 1 | a0001c0001t0001g0269 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1311+4315A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2651147 | ||||||
| chr4:2651160
|
G | A | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1311+4328G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2651160 | ||||||
| chr4:2651330
|
C | CA | 5 | a0001c0001t0001g0123a0001c0001t0001g0152a0001c0001t0001g0231others(2): Show | 5 | HG02572.hp2 HG02647.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1311+4507dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 2651330 | |||||
| chr4:2651366
|
T | C | 12 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1311+4534T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2651366 | ||||||
| chr4:2651536
|
A | G | 1 | a0001c0001t0002g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1311+4704A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2651536 | ||||||
| chr4:2651895
|
A | C | 2 | a0001c0001t0002g0073a0001c0001t0002g0079 | 2 | NA18951.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1311+5063A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2651895 | ||||||
| chr4:2651902
|
G | C | 1 | a0005c0005t0007g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1311+5070G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2651902 | ||||||
| chr4:2651942
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1311+5110C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2651942 | ||||||
| chr4:2652033
|
C | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1311+5201C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2652033 | ||||||
| chr4:2652080
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1311+5248G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2652080 | ||||||
| chr4:2652120
|
A | C | 248 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1311+5288A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2652120 | ||||||
| chr4:2652342
|
G | A | 12 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1312-5461G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2652342 | ||||||
| chr4:2652566
|
G | C | 1 | a0001c0001t0008g0249 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1312-5237G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2652566 | ||||||
| chr4:2652641
|
G | A | 1 | a0003c0003t0005g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1312-5162G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2652641 | ||||||
| chr4:2652659
|
G | A | 1 | a0001c0001t0004g0208 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1312-5144G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2652659 | ||||||
| chr4:2652726
|
C | T | 1 | a0007c0007t0003g0109 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1312-5077C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2652726 | ||||||
| chr4:2652889
|
C | T | 5 | a0002c0014t0001g0270a0008c0009t0001g0266a0008c0009t0001g0295others(2): Show | 5 | NA18944.hp2 NA18947.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312-4914C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2652889 | ||||||
| chr4:2652891
|
A | C | 9 | a0001c0001t0001g0314a0006c0008t0001g0005a0006c0008t0001g0121others(6): Show | 9 | HG00609.hp2 HG02056.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1312-4912A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2652891 | ||||||
| chr4:2652908
|
C | A | 25 | a0001c0001t0001g0176a0001c0021t0003g0143a0003c0003t0001g0235others(22): Show | 25 | HG00609.hp2 HG02145.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1312-4895C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2652908 | ||||||
| chr4:2652914
|
G | T | 1 | a0001c0001t0002g0059 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1312-4889G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2652914 | ||||||
| chr4:2653014
|
G | A | 14 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0030others(11): Show | 14 | HG00438.hp2 HG01934.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.1312-4789G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2653014 | ||||||
| chr4:2653029
|
A | T | 21 | a0001c0001t0002g0015a0001c0001t0002g0050a0001c0002t0016g0023others(18): Show | 21 | HG00408.hp1 HG01074.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1312-4774A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2653029 | ||||||
| chr4:2653188
|
C | A | 9 | a0002c0012t0004g0328a0005c0005t0004g0128a0005c0005t0004g0130others(6): Show | 9 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1312-4615C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2653188 | ||||||
| chr4:2653322
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1312-4481T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2653322 | ||||||
| chr4:2653367
|
C | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1312-4436C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2653367 | ||||||
| chr4:2653479
|
C | G | 2 | a0007c0007t0001g0110a0007c0007t0003g0111 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1312-4324C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2653479 | ||||||
| chr4:2653568
|
C | T | 1 | a0001c0002t0009g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1312-4235C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2653568 | ||||||
| chr4:2653600
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1312-4203C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2653600 | ||||||
| chr4:2653739
|
G | A | 1 | a0003c0003t0005g0187 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1312-4064G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2653739 | ||||||
| chr4:2654062
|
A | G | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1312-3741A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2654062 | ||||||
| chr4:2654152
|
G | A | 1 | a0002c0011t0003g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1312-3651G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2654152 | ||||||
| chr4:2654311
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1312-3492C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2654311 | ||||||
| chr4:2654378
|
A | AT | 38 | a0001c0001t0001g0147a0001c0001t0001g0151a0001c0001t0001g0152others(35): Show | 38 | HG00609.hp1 HG01243.hp1 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.1312-3402dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 2654378 | |||||
| chr4:2654378
|
A | ATT | 35 | a0001c0001t0001g0166a0001c0001t0001g0277a0001c0001t0001g0294others(32): Show | 35 | HG00408.hp1 HG00609.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.1312-3403_1312-340 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 2654378 | |||||
| chr4:2654378
|
A | ATTT | 74 | a0001c0001t0001g0122a0001c0001t0001g0241a0001c0001t0001g0243others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.1312-3404_1312-340 others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 2654378 | |||||
| chr4:2654378
|
A | ATTTT | 7 | a0001c0001t0001g0245a0001c0001t0001g0250a0001c0001t0001g0262others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1312-3405_1312-340 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 2654378 | |||||
| chr4:2654378
|
ATTT | A | 8 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0322others(5): Show | 8 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-3404_1312-340 others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 2654378 | |||||
| chr4:2654527
|
G | A | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1312-3276G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2654527 | ||||||
| chr4:2654589
|
A | C | 11 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(8): Show | 11 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1312-3214A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2654589 | ||||||
| chr4:2654721
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1312-3082A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2654721 | ||||||
| chr4:2654849
|
G | C | 1 | a0001c0001t0001g0264 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1312-2954G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2654849 | ||||||
| chr4:2655424
|
CGT | C | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1312-2367_1312-236 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 2655424 | |||||
| chr4:2655436
|
T | TGC | 23 | a0001c0021t0003g0143a0003c0003t0001g0233a0003c0003t0001g0234others(20): Show | 23 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1312-2365_1312-236 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 2655436 | |||||
| chr4:2655447
|
C | CTG | 5 | a0001c0001t0001g0193a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 5 | HG00609.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312-2338_1312-233 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 2655447 | |||||
| chr4:2655461
|
G | C | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1312-2342G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2655461 | ||||||
| chr4:2655693
|
G | A | 25 | a0001c0021t0003g0143a0003c0003t0001g0233a0003c0003t0001g0234others(22): Show | 25 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1312-2110G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2655693 | ||||||
| chr4:2655715
|
G | T | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1312-2088G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2655715 | ||||||
| chr4:2655732
|
G | A | 25 | a0001c0021t0003g0143a0003c0003t0001g0233a0003c0003t0001g0234others(22): Show | 25 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1312-2071G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2655732 | ||||||
| chr4:2655747
|
A | G | 1 | a0006c0008t0001g0132 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1312-2056A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2655747 | ||||||
| chr4:2655781
|
A | T | 1 | a0001c0001t0002g0088 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1312-2022A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2655781 | ||||||
| chr4:2655828
|
G | A | 1 | a0001c0001t0012g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1312-1975G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2655828 | ||||||
| chr4:2655847
|
T | C | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1312-1956T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2655847 | ||||||
| chr4:2655911
|
A | G | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1312-1892A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2655911 | ||||||
| chr4:2655993
|
C | T | 11 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(8): Show | 11 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1312-1810C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2655993 | ||||||
| chr4:2655997
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1312-1806G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2655997 | ||||||
| chr4:2656032
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1312-1771C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2656032 | ||||||
| chr4:2656084
|
G | A | 9 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(6): Show | 9 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1312-1719G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2656084 | ||||||
| chr4:2656273
|
T | G | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0220 | 3 | NA18940.hp2 NA18956.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1312-1530T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2656273 | ||||||
| chr4:2656321
|
T | C | 1 | a0005c0005t0004g0128 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1312-1482T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2656321 | ||||||
| chr4:2656382
|
A | T | 11 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(8): Show | 11 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1312-1421A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2656382 | ||||||
| chr4:2656600
|
G | A | 99 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1312-1203G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2656600 | ||||||
| chr4:2656743
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1312-1060C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2656743 | ||||||
| chr4:2656938
|
A | C | 1 | a0008c0009t0001g0301 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1312-865A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2656938 | ||||||
| chr4:2656996
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1312-807G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2656996 | ||||||
| chr4:2657028
|
G | C | 99 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1312-775G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2657028 | ||||||
| chr4:2657035
|
C | T | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1312-768C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2657035 | ||||||
| chr4:2657095
|
G | A | 6 | a0003c0003t0004g0155a0003c0003t0005g0164a0003c0003t0005g0188others(3): Show | 6 | HG02257.hp2 HG02572.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1312-708G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2657095 | ||||||
| chr4:2657133
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1312-670A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2657133 | ||||||
| chr4:2657220
|
AT | A | 99 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1312-574delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 2657220 | |||||
| chr4:2657267
|
A | C | 1 | a0001c0001t0002g0098 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1312-536A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2657267 | ||||||
| chr4:2657279
|
C | T | 1 | a0002c0006t0001g0287 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1312-524C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2657279 | ||||||
| chr4:2657500
|
G | A | 1 | a0007c0007t0003g0106 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1312-303G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2657500 | ||||||
| chr4:2657738
|
C | A | 1 | a0001c0001t0001g0065 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1312-65C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 7/20 | chr4 | 2657738 | ||||||
| chr4:2657886
|
C | T | 1 | a0007c0007t0003g0118 | 1 | NA18906.hp2 | splice_region_variant&intron_variant | LOW | c.1389+6C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | chr4 | 2657886 | ||||||
| chr4:2658101
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1389+221A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | chr4 | 2658101 | ||||||
| chr4:2658176
|
T | C | 10 | a0002c0012t0004g0328a0005c0005t0002g0138a0005c0005t0004g0128others(7): Show | 10 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.1389+296T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | chr4 | 2658176 | ||||||
| chr4:2658251
|
C | G | 1 | a0001c0001t0001g0276 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1389+371C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | chr4 | 2658251 | ||||||
| chr4:2658300
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1389+420T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | chr4 | 2658300 | ||||||
| chr4:2658364
|
C | G | 1 | a0001c0001t0004g0208 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1389+484C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | chr4 | 2658364 | ||||||
| chr4:2658598
|
A | G | 24 | a0001c0021t0003g0143a0003c0003t0001g0233a0003c0003t0001g0234others(21): Show | 24 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1389+718A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | chr4 | 2658598 | ||||||
| chr4:2658700
|
T | A | 1 | a0003c0003t0004g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1389+820T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | chr4 | 2658700 | ||||||
| chr4:2658740
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1390-818C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | chr4 | 2658740 | ||||||
| chr4:2658749
|
T | TTTG | 5 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(2): Show | 5 | HG01891.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1390-794_1390-792d others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr4 | 2658749 | |||||
| chr4:2658749
|
TTTG | T | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1390-794_1390-792d others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr4 | 2658749 | |||||
| chr4:2658811
|
C | T | 12 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1390-747C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | chr4 | 2658811 | ||||||
| chr4:2658819
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1390-739C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | chr4 | 2658819 | ||||||
| chr4:2658907
|
C | T | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390-651C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | chr4 | 2658907 | ||||||
| chr4:2659059
|
C | T | 11 | a0002c0012t0004g0328a0005c0005t0004g0128a0005c0005t0004g0130others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.1390-499C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | chr4 | 2659059 | ||||||
| chr4:2659186
|
G | A | 2 | a0001c0001t0002g0035a0001c0001t0002g0087 | 2 | NA18942.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1390-372G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | chr4 | 2659186 | ||||||
| chr4:2659205
|
C | T | 1 | a0003c0003t0004g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1390-353C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | chr4 | 2659205 | ||||||
| chr4:2659512
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1390-46C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 8/20 | chr4 | 2659512 | ||||||
| chr4:2659710
|
G | A | 11 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1502+40G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 9/20 | chr4 | 2659710 | ||||||
| chr4:2660212
|
G | A | 11 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0259others(8): Show | 11 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1745+158G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2660212 | ||||||
| chr4:2660312
|
T | C | 1 | a0001c0001t0002g0084 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1745+258T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2660312 | ||||||
| chr4:2660324
|
C | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1745+270C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2660324 | ||||||
| chr4:2660324
|
C | T | 13 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1745+270C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2660324 | ||||||
| chr4:2660377
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1745+323G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2660377 | ||||||
| chr4:2660430
|
G | A | 13 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1745+376G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2660430 | ||||||
| chr4:2660651
|
C | T | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1745+597C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2660651 | ||||||
| chr4:2660994
|
C | G | 3 | a0001c0001t0001g0261a0001c0001t0001g0265a0001c0001t0001g0289 | 3 | HG02165.hp1 NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1745+940C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2660994 | ||||||
| chr4:2661067
|
TG | T | 65 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(62): Show | 65 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.1745+1014delG | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2661067 | ||||||
| chr4:2661115
|
G | A | 1 | a0003c0003t0001g0236 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1745+1061G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2661115 | ||||||
| chr4:2661319
|
T | G | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1745+1265T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2661319 | ||||||
| chr4:2661374
|
T | A | 2 | a0001c0001t0001g0267a0001c0001t0001g0293 | 2 | NA18946.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1745+1320T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2661374 | ||||||
| chr4:2661490
|
A | G | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1746-1348A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2661490 | ||||||
| chr4:2661868
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1746-970C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2661868 | ||||||
| chr4:2661905
|
C | T | 1 | a0005c0005t0004g0136 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1746-933C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2661905 | ||||||
| chr4:2661936
|
C | T | 99 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1746-902C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2661936 | ||||||
| chr4:2661953
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1746-885G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2661953 | ||||||
| chr4:2661965
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1746-873C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2661965 | ||||||
| chr4:2662024
|
A | C | 3 | a0001c0002t0003g0112a0001c0002t0003g0120a0001c0002t0013g0117 | 3 | HG01516.hp1 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1746-814A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2662024 | ||||||
| chr4:2662052
|
G | A | 9 | a0002c0012t0004g0328a0005c0005t0004g0128a0005c0005t0004g0130others(6): Show | 9 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1746-786G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2662052 | ||||||
| chr4:2662333
|
A | G | 1 | a0005c0005t0004g0141 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1746-505A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2662333 | ||||||
| chr4:2662459
|
C | A | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1746-379C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2662459 | ||||||
| chr4:2662800
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1746-38T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 10/20 | chr4 | 2662800 | ||||||
| chr4:2663034
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1899+43A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 11/20 | chr4 | 2663034 | ||||||
| chr4:2663483
|
A | T | 10 | a0002c0012t0004g0328a0005c0005t0002g0138a0005c0005t0004g0128others(7): Show | 10 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.2079+195A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2663483 | ||||||
| chr4:2663529
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2079+241C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2663529 | ||||||
| chr4:2663688
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2079+400C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2663688 | ||||||
| chr4:2663689
|
G | A | 10 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2079+401G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2663689 | ||||||
| chr4:2663874
|
C | G | 1 | a0002c0012t0004g0328 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2079+586C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2663874 | ||||||
| chr4:2663923
|
C | T | 10 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2079+635C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2663923 | ||||||
| chr4:2664125
|
C | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2079+837C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2664125 | ||||||
| chr4:2664148
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2079+860C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2664148 | ||||||
| chr4:2664274
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2079+986G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2664274 | ||||||
| chr4:2664388
|
G | A | 1 | a0003c0003t0011g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2079+1100G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2664388 | ||||||
| chr4:2664393
|
G | A | 12 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2079+1105G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2664393 | ||||||
| chr4:2664415
|
G | A | 1 | a0001c0001t0001g0276 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2079+1127G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2664415 | ||||||
| chr4:2664549
|
A | T | 243 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.2079+1261A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2664549 | ||||||
| chr4:2664558
|
C | CT | 74 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0151others(71): Show | 74 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.2079+1296dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 2664558 | |||||
| chr4:2664558
|
C | CTT | 67 | a0001c0001t0001g0166a0001c0001t0001g0241a0001c0001t0001g0244others(64): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.2079+1295_2079+129 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 2664558 | |||||
| chr4:2664558
|
C | CTTT | 12 | a0001c0001t0001g0243a0001c0001t0001g0245a0001c0001t0001g0246others(9): Show | 12 | HG00544.hp2 HG00735.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2079+1294_2079+129 others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 2664558 | |||||
| chr4:2664558
|
CT | C | 10 | a0001c0001t0001g0185a0001c0001t0002g0033a0001c0001t0002g0041others(7): Show | 10 | HG00558.hp2 HG01081.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.2079+1296delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 2664558 | |||||
| chr4:2664558
|
CTT | C | 9 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(6): Show | 9 | HG02257.hp1 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2079+1295_2079+129 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 2664558 | |||||
| chr4:2664562
|
T | C | 7 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(4): Show | 7 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2079+1274T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2664562 | ||||||
| chr4:2664563
|
T | C | 1 | a0006c0008t0001g0216 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2079+1275T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2664563 | ||||||
| chr4:2664628
|
G | A | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2079+1340G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2664628 | ||||||
| chr4:2664629
|
C | T | 3 | a0006c0008t0001g0127a0006c0008t0001g0132a0006c0008t0001g0216 | 3 | HG02818.hp1 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2079+1341C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2664629 | ||||||
| chr4:2664636
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2079+1348G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2664636 | ||||||
| chr4:2664653
|
C | G | 262 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(259): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2079+1365C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2664653 | ||||||
| chr4:2664795
|
C | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2079+1507C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2664795 | ||||||
| chr4:2664806
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2079+1518G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2664806 | ||||||
| chr4:2664847
|
G | T | 1 | a0003c0003t0005g0187 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2079+1559G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2664847 | ||||||
| chr4:2665006
|
C | G | 3 | a0001c0001t0001g0261a0001c0001t0001g0265a0001c0001t0001g0289 | 3 | HG02165.hp1 NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2079+1718C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2665006 | ||||||
| chr4:2665056
|
T | C | 2 | a0004c0004t0001g0318a0004c0004t0001g0322 | 2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2079+1768T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2665056 | ||||||
| chr4:2665079
|
A | G | 1 | a0006c0008t0001g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2079+1791A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2665079 | ||||||
| chr4:2665165
|
T | TA | 15 | a0001c0001t0001g0123a0001c0001t0001g0142a0001c0001t0001g0144others(12): Show | 15 | HG00408.hp2 HG00438.hp1 NA18945.hp2 others(12): Show |
intron_variant | MODIFIER | c.2079+1884dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 2665165 | |||||
| chr4:2665172
|
A | T | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2079+1884A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2665172 | ||||||
| chr4:2665349
|
T | A | 2 | a0001c0001t0002g0024a0001c0001t0002g0025 | 2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.2079+2061T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2665349 | ||||||
| chr4:2665739
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2079+2451C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2665739 | ||||||
| chr4:2665765
|
C | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2079+2477C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2665765 | ||||||
| chr4:2665845
|
G | A | 242 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.2079+2557G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2665845 | ||||||
| chr4:2665869
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2079+2581C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2665869 | ||||||
| chr4:2665887
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2079+2599C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2665887 | ||||||
| chr4:2666151
|
G | A | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2079+2863G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2666151 | ||||||
| chr4:2666246
|
G | A | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2079+2958G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2666246 | ||||||
| chr4:2666265
|
C | T | 4 | a0001c0001t0001g0146a0001c0001t0001g0202a0001c0001t0001g0204others(1): Show | 4 | NA18989.hp1 NA18999.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.2079+2977C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2666265 | ||||||
| chr4:2666357
|
C | A | 20 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(17): Show | 20 | HG00609.hp2 HG02145.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.2079+3069C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2666357 | ||||||
| chr4:2666490
|
C | A | 175 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(172): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.2079+3202C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2666490 | ||||||
| chr4:2666503
|
T | C | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2079+3215T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2666503 | ||||||
| chr4:2666829
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2079+3541C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2666829 | ||||||
| chr4:2667234
|
C | G | 8 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0159others(5): Show | 8 | HG00408.hp2 HG00438.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.2079+3946C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2667234 | ||||||
| chr4:2667327
|
T | C | 101 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.2079+4039T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2667327 | ||||||
| chr4:2667520
|
T | C | 1 | a0001c0001t0004g0208 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2079+4232T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2667520 | ||||||
| chr4:2667682
|
T | C | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2079+4394T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2667682 | ||||||
| chr4:2667857
|
A | C | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2080-4264A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2667857 | ||||||
| chr4:2667862
|
C | T | 1 | a0008c0009t0001g0266 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2080-4259C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2667862 | ||||||
| chr4:2667883
|
A | T | 1 | a0001c0001t0002g0075 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2080-4238A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2667883 | ||||||
| chr4:2667930
|
G | T | 1 | a0001c0001t0002g0006 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2080-4191G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2667930 | ||||||
| chr4:2667932
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2080-4189C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2667932 | ||||||
| chr4:2668213
|
C | CT | 23 | a0001c0001t0001g0004a0001c0001t0001g0201a0001c0001t0001g0203others(20): Show | 23 | HG00408.hp1 HG00609.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.2080-3890dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 2668213 | |||||
| chr4:2668213
|
CT | C | 30 | a0001c0001t0001g0185a0001c0001t0001g0207a0001c0001t0001g0283others(27): Show | 30 | HG00558.hp1 HG01081.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.2080-3890delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 2668213 | |||||
| chr4:2668278
|
A | G | 2 | a0004c0004t0001g0323a0004c0004t0001g0327 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2080-3843A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2668278 | ||||||
| chr4:2668403
|
A | G | 2 | a0004c0004t0001g0323a0004c0004t0001g0327 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2080-3718A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2668403 | ||||||
| chr4:2668412
|
C | T | 11 | a0002c0012t0004g0328a0005c0005t0002g0138a0005c0005t0004g0128others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.2080-3709C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2668412 | ||||||
| chr4:2668434
|
T | G | 262 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(259): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2080-3687T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2668434 | ||||||
| chr4:2668459
|
C | T | 11 | a0002c0012t0004g0328a0005c0005t0002g0138a0005c0005t0004g0128others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.2080-3662C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2668459 | ||||||
| chr4:2668579
|
A | C | 13 | a0001c0001t0001g0231a0001c0001t0001g0232a0002c0012t0004g0328others(10): Show | 13 | HG00408.hp1 HG01074.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2080-3542A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2668579 | ||||||
| chr4:2668648
|
C | A | 1 | a0001c0001t0004g0191 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2080-3473C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2668648 | ||||||
| chr4:2668732
|
A | G | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2080-3389A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2668732 | ||||||
| chr4:2668779
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2080-3342C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2668779 | ||||||
| chr4:2668823
|
CCTTTTCC others(4): Show |
C | 10 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(7): Show | 10 | HG00609.hp2 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2080-3286_2080-327 others(15): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 2668823 | |||||
| chr4:2668830
|
C | CTTTTCTT others(5): Show |
2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG00639.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.2080-3274_2080-326 others(16): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 2668830 | |||||
| chr4:2669005
|
G | C | 12 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2080-3116G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2669005 | ||||||
| chr4:2669157
|
G | A | 9 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(6): Show | 9 | HG02145.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2080-2964G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2669157 | ||||||
| chr4:2669213
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2080-2908C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2669213 | ||||||
| chr4:2669288
|
G | C | 246 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.2080-2833G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2669288 | ||||||
| chr4:2669342
|
G | C | 15 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0030others(12): Show | 15 | HG00438.hp2 HG01934.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.2080-2779G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2669342 | ||||||
| chr4:2669379
|
C | T | 100 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.2080-2742C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2669379 | ||||||
| chr4:2669395
|
G | C | 4 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.2080-2726G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2669395 | ||||||
| chr4:2669406
|
C | T | 2 | a0001c0001t0001g0277a0001c0001t0001g0281 | 2 | NA18957.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2080-2715C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2669406 | ||||||
| chr4:2669533
|
C | T | 1 | a0010c0022t0001g0227 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2080-2588C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2669533 | ||||||
| chr4:2669534
|
G | A | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2080-2587G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2669534 | ||||||
| chr4:2669628
|
TA | T | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2080-2490delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr4 | 2669628 | |||||
| chr4:2669988
|
A | G | 9 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(6): Show | 9 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2080-2133A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2669988 | ||||||
| chr4:2670120
|
A | G | 1 | a0003c0003t0011g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2080-2001A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2670120 | ||||||
| chr4:2670676
|
G | T | 21 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(18): Show | 21 | HG00609.hp2 HG02145.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.2080-1445G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2670676 | ||||||
| chr4:2670751
|
C | T | 1 | a0001c0001t0012g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2080-1370C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2670751 | ||||||
| chr4:2670922
|
C | T | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2080-1199C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2670922 | ||||||
| chr4:2671064
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2080-1057T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2671064 | ||||||
| chr4:2671084
|
G | T | 4 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0304others(1): Show | 4 | HG02004.hp2 HG02630.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2080-1037G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2671084 | ||||||
| chr4:2671165
|
C | G | 1 | a0001c0001t0001g0144 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2080-956C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2671165 | ||||||
| chr4:2671258
|
A | C | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2080-863A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2671258 | ||||||
| chr4:2671496
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2080-625G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2671496 | ||||||
| chr4:2671585
|
G | A | 2 | a0001c0001t0001g0219a0010c0022t0001g0227 | 2 | HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2080-536G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2671585 | ||||||
| chr4:2671713
|
G | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0146a0001c0001t0001g0201others(6): Show | 9 | HG00609.hp1 HG02040.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.2080-408G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2671713 | ||||||
| chr4:2671744
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2080-377G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2671744 | ||||||
| chr4:2672002
|
C | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2080-119C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 12/20 | chr4 | 2672002 | ||||||
| chr4:2672544
|
G | T | 165 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.2331+172G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2672544 | ||||||
| chr4:2672634
|
A | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2331+262A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2672634 | ||||||
| chr4:2672674
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2331+302A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2672674 | ||||||
| chr4:2673161
|
CT | C | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2331+797delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2673161 | |||||
| chr4:2673286
|
G | A | 4 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0085others(1): Show | 4 | HG00323.hp2 HG01099.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.2331+914G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2673286 | ||||||
| chr4:2673292
|
G | A | 1 | a0002c0012t0004g0328 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2331+920G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2673292 | ||||||
| chr4:2673464
|
T | C | 12 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2331+1092T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2673464 | ||||||
| chr4:2673492
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2331+1120A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2673492 | ||||||
| chr4:2673627
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2331+1255C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2673627 | ||||||
| chr4:2673638
|
G | A | 4 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.2331+1266G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2673638 | ||||||
| chr4:2673655
|
AT | A | 12 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2331+1287delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2673655 | |||||
| chr4:2673810
|
A | G | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2331+1438A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2673810 | ||||||
| chr4:2673869
|
G | A | 1 | a0001c0001t0002g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2331+1497G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2673869 | ||||||
| chr4:2674038
|
C | T | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2331+1666C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2674038 | ||||||
| chr4:2674148
|
G | T | 1 | a0001c0001t0002g0008 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2331+1776G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2674148 | ||||||
| chr4:2674166
|
A | G | 102 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.2331+1794A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2674166 | ||||||
| chr4:2674283
|
T | G | 1 | a0001c0001t0001g0160 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2331+1911T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2674283 | ||||||
| chr4:2674289
|
G | C | 101 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.2331+1917G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2674289 | ||||||
| chr4:2674295
|
GT | G | 13 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(10): Show | 13 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2331+1925delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2674295 | |||||
| chr4:2674510
|
G | C | 1 | a0001c0001t0001g0304 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2331+2138G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2674510 | ||||||
| chr4:2674616
|
G | T | 4 | a0001c0001t0001g0178a0001c0001t0001g0185a0001c0001t0001g0217others(1): Show | 4 | HG00639.hp2 HG01081.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2331+2244G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2674616 | ||||||
| chr4:2674711
|
A | G | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2331+2339A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2674711 | ||||||
| chr4:2674833
|
C | CA | 15 | a0001c0001t0001g0178a0001c0001t0001g0194a0001c0001t0002g0009others(12): Show | 15 | HG00408.hp1 HG01074.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2331+2480dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2674833 | |||||
| chr4:2674833
|
CA | C | 9 | a0001c0001t0001g0152a0001c0001t0001g0167a0001c0001t0001g0225others(6): Show | 9 | HG00323.hp2 HG02647.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.2331+2480delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2674833 | |||||
| chr4:2674833
|
CAAAAAAA others(1): Show |
C | 55 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(52): Show | 55 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.2331+2473_2331+248 others(12): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2674833 | |||||
| chr4:2675130
|
G | T | 4 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0330others(1): Show | 4 | HG00733.hp2 HG03927.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.2331+2758G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2675130 | ||||||
| chr4:2675163
|
T | A | 22 | a0001c0021t0003g0143a0002c0012t0004g0328a0004c0004t0001g0318others(19): Show | 22 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.2331+2791T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2675163 | ||||||
| chr4:2675245
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2331+2873C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2675245 | ||||||
| chr4:2675345
|
C | T | 1 | a0001c0002t0009g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2331+2973C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2675345 | ||||||
| chr4:2675421
|
A | G | 22 | a0001c0021t0003g0143a0002c0012t0004g0328a0004c0004t0001g0318others(19): Show | 22 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.2331+3049A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2675421 | ||||||
| chr4:2675639
|
G | T | 1 | a0001c0001t0001g0286 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2331+3267G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2675639 | ||||||
| chr4:2675851
|
C | T | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2331+3479C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2675851 | ||||||
| chr4:2675986
|
A | G | 1 | a0001c0001t0002g0094 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2331+3614A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2675986 | ||||||
| chr4:2676074
|
G | A | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2331+3702G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676074 | ||||||
| chr4:2676146
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2331+3774G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676146 | ||||||
| chr4:2676214
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2331+3842G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676214 | ||||||
| chr4:2676277
|
A | G | 12 | a0001c0001t0008g0215a0002c0012t0004g0328a0005c0005t0004g0128others(9): Show | 12 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.2331+3905A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676277 | ||||||
| chr4:2676384
|
A | G | 1 | a0001c0002t0009g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2331+4012A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676384 | ||||||
| chr4:2676433
|
T | G | 1 | a0001c0001t0002g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2331+4061T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676433 | ||||||
| chr4:2676481
|
A | C | 68 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.2331+4109A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676481 | ||||||
| chr4:2676560
|
T | C | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2331+4188T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676560 | ||||||
| chr4:2676681
|
G | A | 9 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(6): Show | 9 | HG02145.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2331+4309G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676681 | ||||||
| chr4:2676711
|
G | A | 1 | a0002c0012t0004g0328 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2331+4339G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676711 | ||||||
| chr4:2676791
|
ATT | A | 4 | a0001c0001t0002g0056a0001c0001t0002g0059a0001c0001t0002g0095others(1): Show | 4 | HG02015.hp2 HG02040.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2331+4420_2331+442 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676791 | ||||||
| chr4:2676798
|
G | A | 1 | a0001c0001t0002g0048 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2331+4426G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676798 | ||||||
| chr4:2676849
|
G | A | 3 | a0001c0001t0008g0215a0009c0010t0014g0228a0009c0010t0015g0229 | 3 | HG02486.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2331+4477G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676849 | ||||||
| chr4:2676851
|
A | G | 14 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(11): Show | 14 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2331+4479A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676851 | ||||||
| chr4:2676856
|
G | A | 1 | a0003c0003t0004g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2331+4484G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676856 | ||||||
| chr4:2676858
|
G | A | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2331+4486G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676858 | ||||||
| chr4:2676898
|
G | A | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2331+4526G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676898 | ||||||
| chr4:2676918
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2331+4546G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2676918 | ||||||
| chr4:2677019
|
A | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2331+4647A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677019 | ||||||
| chr4:2677019
|
A | T | 9 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(6): Show | 9 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2331+4647A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677019 | ||||||
| chr4:2677058
|
C | T | 14 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(11): Show | 14 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2331+4686C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677058 | ||||||
| chr4:2677074
|
G | A | 5 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0166others(2): Show | 5 | HG00639.hp1 HG01175.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.2331+4702G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677074 | ||||||
| chr4:2677095
|
T | A | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2331+4723T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677095 | ||||||
| chr4:2677403
|
GTTGTT | G | 14 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(11): Show | 14 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2331+5054_2331+505 others(9): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2677403 | |||||
| chr4:2677440
|
T | G | 1 | a0001c0001t0001g0200 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2331+5068T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677440 | ||||||
| chr4:2677462
|
C | T | 2 | a0001c0001t0002g0330a0002c0006t0002g0046 | 2 | HG03927.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2331+5090C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677462 | ||||||
| chr4:2677465
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2331+5093G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677465 | ||||||
| chr4:2677509
|
G | A | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2331+5137G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677509 | ||||||
| chr4:2677515
|
C | T | 1 | a0005c0005t0004g0128 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2331+5143C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677515 | ||||||
| chr4:2677565
|
C | T | 4 | a0001c0001t0002g0011a0001c0001t0002g0040a0001c0001t0002g0047others(1): Show | 4 | NA18967.hp1 NA18970.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2331+5193C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677565 | ||||||
| chr4:2677665
|
C | T | 12 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2331+5293C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677665 | ||||||
| chr4:2677675
|
A | G | 32 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(29): Show | 32 | HG00408.hp1 HG01074.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.2331+5303A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677675 | ||||||
| chr4:2677741
|
C | CA | 28 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(25): Show | 28 | HG00738.hp1 HG01243.hp2 HG01516.hp1 others(25): Show |
intron_variant | MODIFIER | c.2331+5386dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2677741 | |||||
| chr4:2677741
|
C | CAA | 9 | a0001c0002t0016g0023a0007c0007t0001g0110a0007c0007t0001g0115others(6): Show | 9 | HG01891.hp1 HG02717.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2331+5385_2331+538 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2677741 | |||||
| chr4:2677743
|
A | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2331+5371A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677743 | ||||||
| chr4:2677794
|
A | G | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2331+5422A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677794 | ||||||
| chr4:2677842
|
C | G | 14 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(11): Show | 14 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2331+5470C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677842 | ||||||
| chr4:2677898
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2331+5526G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677898 | ||||||
| chr4:2677937
|
G | A | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2331+5565G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2677937 | ||||||
| chr4:2677995
|
GTGTT | G | 12 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2331+5642_2331+564 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2677995 | |||||
| chr4:2678098
|
A | G | 10 | a0002c0012t0004g0328a0005c0005t0004g0128a0005c0005t0004g0130others(7): Show | 10 | HG00408.hp1 HG01074.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2331+5726A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2678098 | ||||||
| chr4:2678142
|
C | T | 10 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(7): Show | 10 | HG00609.hp2 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2331+5770C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2678142 | ||||||
| chr4:2678263
|
C | T | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2331+5891C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2678263 | ||||||
| chr4:2678343
|
T | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2331+5971T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2678343 | ||||||
| chr4:2678359
|
G | GGT | 3 | a0004c0004t0001g0321a0004c0004t0003g0317a0004c0004t0003g0319 | 3 | HG02630.hp2 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2331+5988_2331+598 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2678359 | |||||
| chr4:2678360
|
G | GT | 30 | a0001c0001t0001g0146a0001c0001t0001g0152a0001c0001t0001g0175others(27): Show | 30 | HG01192.hp2 HG01243.hp1 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.2331+6008dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2678360 | |||||
| chr4:2678360
|
G | GTT | 12 | a0001c0001t0001g0245a0001c0001t0001g0288a0001c0001t0002g0076others(9): Show | 12 | HG00408.hp1 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2331+6007_2331+600 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2678360 | |||||
| chr4:2678360
|
G | T | 6 | a0001c0001t0001g0252a0001c0001t0001g0271a0001c0001t0001g0272others(3): Show | 6 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(3): Show |
intron_variant | MODIFIER | c.2331+5988G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2678360 | ||||||
| chr4:2678368
|
T | G | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2331+5996T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2678368 | ||||||
| chr4:2678465
|
C | T | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2331+6093C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2678465 | ||||||
| chr4:2678543
|
A | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2331+6171A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2678543 | ||||||
| chr4:2678626
|
G | T | 1 | a0001c0001t0001g0184 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2331+6254G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2678626 | ||||||
| chr4:2678688
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2331+6316G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2678688 | ||||||
| chr4:2678722
|
A | G | 1 | a0001c0002t0003g0112 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2331+6350A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2678722 | ||||||
| chr4:2678785
|
C | T | 1 | a0001c0002t0001g0001 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2331+6413C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2678785 | ||||||
| chr4:2678788
|
T | C | 102 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.2331+6416T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2678788 | ||||||
| chr4:2678791
|
T | C | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2331+6419T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2678791 | ||||||
| chr4:2679294
|
C | G | 1 | a0001c0002t0001g0003 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2331+6922C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2679294 | ||||||
| chr4:2679294
|
C | T | 5 | a0002c0014t0001g0270a0008c0009t0001g0266a0008c0009t0001g0295others(2): Show | 5 | NA18944.hp2 NA18947.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.2331+6922C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2679294 | ||||||
| chr4:2679307
|
G | T | 14 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(11): Show | 14 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2331+6935G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2679307 | ||||||
| chr4:2679357
|
T | A | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2331+6985T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2679357 | ||||||
| chr4:2679375
|
C | CT | 29 | a0001c0001t0001g0162a0001c0001t0001g0193a0001c0001t0001g0245others(26): Show | 29 | HG00280.hp1 HG00323.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.2331+7027dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2679375 | |||||
| chr4:2679375
|
CT | C | 33 | a0001c0001t0001g0065a0001c0001t0001g0207a0001c0001t0001g0220others(30): Show | 33 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.2331+7027delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2679375 | |||||
| chr4:2679375
|
CTTTTTTT others(5): Show |
C | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2331+7016_2331+702 others(16): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2679375 | |||||
| chr4:2679379
|
T | C | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2331+7007T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2679379 | ||||||
| chr4:2679382
|
T | C | 3 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0008g0215 | 3 | HG03139.hp1 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2331+7010T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2679382 | ||||||
| chr4:2679860
|
AT | A | 56 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(53): Show | 56 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.2331+7501delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2679860 | |||||
| chr4:2679945
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2331+7573C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2679945 | ||||||
| chr4:2679958
|
CT | C | 14 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(11): Show | 14 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2331+7587delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2679958 | ||||||
| chr4:2679963
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2331+7591C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2679963 | ||||||
| chr4:2680062
|
T | C | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2331+7690T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2680062 | ||||||
| chr4:2680451
|
C | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2331+8079C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2680451 | ||||||
| chr4:2680523
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2331+8151G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2680523 | ||||||
| chr4:2680528
|
G | A | 1 | a0006c0008t0001g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2331+8156G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2680528 | ||||||
| chr4:2680533
|
C | T | 1 | a0004c0017t0001g0324 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2331+8161C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2680533 | ||||||
| chr4:2680537
|
A | G | 3 | a0001c0001t0008g0215a0009c0010t0014g0228a0009c0010t0015g0229 | 3 | HG02486.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2331+8165A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2680537 | ||||||
| chr4:2680551
|
G | A | 3 | a0001c0001t0002g0026a0001c0001t0002g0027a0015c0015t0002g0028 | 3 | HG00099.hp1 HG00280.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.2331+8179G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2680551 | ||||||
| chr4:2680635
|
C | A | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2331+8263C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2680635 | ||||||
| chr4:2680648
|
A | T | 14 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(11): Show | 14 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2331+8276A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2680648 | ||||||
| chr4:2680649
|
C | CT | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2331+8287dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2680649 | |||||
| chr4:2680655
|
T | C | 1 | a0001c0001t0006g0052 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2331+8283T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2680655 | ||||||
| chr4:2680787
|
G | T | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2331+8415G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2680787 | ||||||
| chr4:2680802
|
C | T | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0329 | 3 | HG01106.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2331+8430C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2680802 | ||||||
| chr4:2680858
|
T | C | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0329 | 3 | HG01106.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2331+8486T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2680858 | ||||||
| chr4:2680870
|
G | C | 3 | a0007c0007t0003g0106a0007c0007t0003g0107a0007c0007t0003g0108 | 3 | HG01891.hp1 HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2331+8498G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2680870 | ||||||
| chr4:2680936
|
C | T | 100 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.2331+8564C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2680936 | ||||||
| chr4:2681016
|
T | C | 14 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(11): Show | 14 | HG01167.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2332-8490T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2681016 | ||||||
| chr4:2681275
|
C | T | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2332-8231C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2681275 | ||||||
| chr4:2681328
|
A | G | 24 | a0001c0001t0008g0249a0001c0002t0001g0001a0001c0002t0001g0002others(21): Show | 24 | HG01109.hp1 HG01243.hp2 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.2332-8178A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2681328 | ||||||
| chr4:2681352
|
T | C | 13 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2332-8154T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2681352 | ||||||
| chr4:2681433
|
G | A | 1 | a0001c0001t0002g0098 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2332-8073G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2681433 | ||||||
| chr4:2681506
|
A | G | 77 | a0001c0001t0001g0122a0001c0001t0001g0241a0001c0001t0001g0243others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.2332-8000A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2681506 | ||||||
| chr4:2681609
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2332-7897C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2681609 | ||||||
| chr4:2681673
|
A | C | 31 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(28): Show | 31 | HG00408.hp1 HG01074.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.2332-7833A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2681673 | ||||||
| chr4:2681709
|
C | G | 13 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2332-7797C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2681709 | ||||||
| chr4:2681853
|
G | A | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2332-7653G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2681853 | ||||||
| chr4:2681969
|
A | AG | 9 | a0001c0021t0003g0143a0004c0004t0001g0321a0004c0004t0001g0323others(6): Show | 9 | HG02145.hp1 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2332-7534dupG | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2681969 | |||||
| chr4:2681972
|
G | GT | 10 | a0001c0001t0001g0194a0001c0001t0001g0212a0001c0001t0002g0035others(7): Show | 10 | HG01975.hp2 HG02109.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.2332-7521dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2681972 | |||||
| chr4:2681982
|
T | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2332-7524T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2681982 | ||||||
| chr4:2681986
|
G | GT | 3 | a0006c0008t0001g0127a0006c0008t0001g0132a0006c0008t0001g0216 | 3 | HG02818.hp1 HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2332-7520_2332-751 others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2681986 | ||||||
| chr4:2681987
|
G | GT | 13 | a0001c0001t0001g0123a0001c0001t0001g0159a0001c0001t0001g0166others(10): Show | 13 | HG00438.hp2 HG00733.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.2332-7504dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2681987 | |||||
| chr4:2681987
|
G | GTT | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2332-7505_2332-750 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2681987 | |||||
| chr4:2681987
|
G | T | 10 | a0001c0001t0001g0264a0001c0001t0008g0215a0006c0008t0001g0005others(7): Show | 10 | HG00609.hp2 HG02559.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.2332-7519G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2681987 | ||||||
| chr4:2681987
|
GT | G | 8 | a0001c0001t0001g0253a0003c0003t0004g0155a0003c0003t0005g0164others(5): Show | 8 | HG01167.hp1 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2332-7504delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2681987 | |||||
| chr4:2681989
|
T | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2332-7517T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2681989 | ||||||
| chr4:2682017
|
C | T | 1 | a0001c0001t0002g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2332-7489C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682017 | ||||||
| chr4:2682020
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2332-7486G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682020 | ||||||
| chr4:2682047
|
C | T | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2332-7459C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682047 | ||||||
| chr4:2682125
|
C | T | 1 | a0008c0009t0001g0301 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2332-7381C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682125 | ||||||
| chr4:2682146
|
G | A | 2 | a0004c0004t0001g0318a0004c0004t0001g0322 | 2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2332-7360G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682146 | ||||||
| chr4:2682170
|
A | G | 1 | a0001c0001t0002g0009 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2332-7336A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682170 | ||||||
| chr4:2682184
|
C | G | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2332-7322C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682184 | ||||||
| chr4:2682337
|
T | G | 4 | a0004c0004t0001g0321a0004c0004t0003g0317a0004c0004t0003g0319others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2332-7169T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682337 | ||||||
| chr4:2682350
|
G | C | 1 | a0001c0002t0003g0112 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2332-7156G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682350 | ||||||
| chr4:2682383
|
T | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2332-7123T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682383 | ||||||
| chr4:2682395
|
C | T | 1 | a0006c0008t0001g0125 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2332-7111C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682395 | ||||||
| chr4:2682529
|
G | T | 1 | a0002c0006t0001g0242 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2332-6977G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682529 | ||||||
| chr4:2682576
|
T | C | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2332-6930T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682576 | ||||||
| chr4:2682706
|
A | G | 6 | a0003c0003t0005g0164a0003c0003t0005g0187a0003c0003t0005g0188others(3): Show | 6 | HG02257.hp2 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2332-6800A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682706 | ||||||
| chr4:2682728
|
A | T | 1 | a0001c0001t0001g0205 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2332-6778A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682728 | ||||||
| chr4:2682832
|
CAT | C | 100 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.2332-6673_2332-667 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682832 | ||||||
| chr4:2682855
|
A | T | 68 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0008g0215others(65): Show | 68 | HG00408.hp1 HG00609.hp2 HG01074.hp1 others(65): Show |
intron_variant | MODIFIER | c.2332-6651A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682855 | ||||||
| chr4:2682897
|
TAAG | T | 3 | a0001c0021t0003g0143a0004c0004t0001g0323a0004c0004t0001g0327 | 3 | HG02145.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2332-6601_2332-659 others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2682897 | |||||
| chr4:2682937
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2332-6569G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2682937 | ||||||
| chr4:2683199
|
A | G | 1 | a0001c0001t0002g0083 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2332-6307A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2683199 | ||||||
| chr4:2683245
|
G | A | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2332-6261G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2683245 | ||||||
| chr4:2683284
|
C | CT | 14 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0032others(11): Show | 14 | HG00323.hp2 HG00558.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.2332-6208dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2683284 | |||||
| chr4:2683286
|
T | C | 1 | a0001c0001t0002g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2332-6220T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2683286 | ||||||
| chr4:2683333
|
C | T | 3 | a0001c0001t0002g0056a0001c0001t0002g0095a0001c0001t0002g0101 | 3 | HG02015.hp2 HG02040.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2332-6173C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2683333 | ||||||
| chr4:2683358
|
C | T | 9 | a0002c0012t0004g0328a0005c0005t0004g0128a0005c0005t0004g0130others(6): Show | 9 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.2332-6148C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2683358 | ||||||
| chr4:2683793
|
T | C | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2332-5713T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2683793 | ||||||
| chr4:2684024
|
C | T | 3 | a0001c0001t0008g0215a0009c0010t0014g0228a0009c0010t0015g0229 | 3 | HG02486.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2332-5482C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2684024 | ||||||
| chr4:2684162
|
C | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2332-5344C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2684162 | ||||||
| chr4:2684302
|
T | C | 1 | a0003c0003t0001g0238 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2332-5204T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2684302 | ||||||
| chr4:2684360
|
A | T | 1 | a0001c0001t0002g0013 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2332-5146A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2684360 | ||||||
| chr4:2684425
|
G | GT | 17 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0008g0215others(14): Show | 17 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.2332-5071dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2684425 | |||||
| chr4:2684464
|
C | T | 9 | a0001c0001t0001g0251a0001c0001t0001g0258a0001c0001t0001g0278others(6): Show | 9 | HG01099.hp2 HG01106.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.2332-5042C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2684464 | ||||||
| chr4:2684562
|
TTA | T | 3 | a0001c0001t0008g0215a0009c0010t0014g0228a0009c0010t0015g0229 | 3 | HG02486.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2332-4942_2332-494 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2684562 | |||||
| chr4:2684608
|
T | C | 78 | a0001c0001t0001g0122a0001c0001t0001g0241a0001c0001t0001g0243others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2332-4898T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2684608 | ||||||
| chr4:2684617
|
C | G | 1 | a0001c0001t0002g0104 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2332-4889C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2684617 | ||||||
| chr4:2684617
|
C | T | 3 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0286 | 3 | HG00140.hp2 HG01167.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2332-4889C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2684617 | ||||||
| chr4:2684641
|
A | G | 1 | a0008c0009t0001g0310 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2332-4865A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2684641 | ||||||
| chr4:2684701
|
C | T | 1 | a0015c0015t0002g0028 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2332-4805C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2684701 | ||||||
| chr4:2684760
|
A | G | 1 | a0005c0005t0004g0141 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2332-4746A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2684760 | ||||||
| chr4:2684792
|
C | G | 1 | a0001c0001t0001g0230 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2332-4714C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2684792 | ||||||
| chr4:2684798
|
C | T | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2332-4708C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2684798 | ||||||
| chr4:2684897
|
C | T | 1 | a0001c0001t0002g0330 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2332-4609C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2684897 | ||||||
| chr4:2685277
|
G | A | 20 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(17): Show | 20 | HG00609.hp2 HG01891.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.2332-4229G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2685277 | ||||||
| chr4:2685364
|
G | A | 245 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.2332-4142G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2685364 | ||||||
| chr4:2685403
|
G | T | 1 | a0003c0003t0004g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2332-4103G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2685403 | ||||||
| chr4:2685717
|
C | T | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2332-3789C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2685717 | ||||||
| chr4:2685745
|
A | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2332-3761A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2685745 | ||||||
| chr4:2685757
|
C | T | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2332-3749C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2685757 | ||||||
| chr4:2685766
|
G | A | 7 | a0003c0003t0004g0155a0003c0003t0005g0164a0003c0003t0005g0187others(4): Show | 7 | HG02257.hp2 HG02572.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2332-3740G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2685766 | ||||||
| chr4:2685784
|
G | A | 1 | a0001c0001t0004g0196 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2332-3722G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2685784 | ||||||
| chr4:2685794
|
T | C | 246 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.2332-3712T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2685794 | ||||||
| chr4:2685852
|
T | A | 14 | a0001c0001t0001g0004a0001c0001t0001g0145a0001c0001t0001g0146others(11): Show | 14 | HG00558.hp1 HG00609.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.2332-3654T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2685852 | ||||||
| chr4:2685943
|
C | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2332-3563C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2685943 | ||||||
| chr4:2685996
|
A | G | 5 | a0001c0001t0002g0035a0001c0001t0002g0039a0001c0001t0002g0070others(2): Show | 5 | NA18612.hp2 NA18942.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.2332-3510A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2685996 | ||||||
| chr4:2686002
|
T | A | 1 | a0005c0005t0004g0128 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2332-3504T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2686002 | ||||||
| chr4:2686335
|
T | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2332-3171T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2686335 | ||||||
| chr4:2686473
|
A | T | 1 | a0001c0001t0002g0045 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2332-3033A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2686473 | ||||||
| chr4:2686571
|
CTGA | C | 34 | a0001c0001t0001g0250a0001c0001t0008g0215a0001c0021t0003g0143others(31): Show | 34 | HG00609.hp2 HG01891.hp2 HG02145.hp1 others(31): Show |
intron_variant | MODIFIER | c.2332-2931_2332-292 others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2686571 | |||||
| chr4:2686676
|
C | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2332-2830C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2686676 | ||||||
| chr4:2686680
|
G | A | 3 | a0001c0002t0003g0112a0001c0002t0003g0120a0001c0002t0013g0117 | 3 | HG01516.hp1 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2332-2826G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2686680 | ||||||
| chr4:2686763
|
C | G | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2332-2743C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2686763 | ||||||
| chr4:2686788
|
G | T | 1 | a0001c0001t0002g0035 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2332-2718G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2686788 | ||||||
| chr4:2686992
|
A | G | 8 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0051others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2332-2514A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2686992 | ||||||
| chr4:2687220
|
A | C | 3 | a0001c0001t0001g0133a0001c0001t0002g0010a0001c0001t0002g0062 | 3 | HG02080.hp1 HG02132.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2332-2286A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2687220 | ||||||
| chr4:2687279
|
A | G | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2332-2227A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2687279 | ||||||
| chr4:2687334
|
A | G | 36 | a0001c0001t0001g0152a0001c0001t0001g0231a0001c0001t0001g0232others(33): Show | 36 | HG00408.hp1 HG01074.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.2332-2172A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2687334 | ||||||
| chr4:2687489
|
C | G | 1 | a0006c0008t0001g0125 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2332-2017C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2687489 | ||||||
| chr4:2687570
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2332-1936G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2687570 | ||||||
| chr4:2687586
|
G | A | 2 | a0001c0001t0007g0129a0001c0001t0007g0137 | 2 | HG01167.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2332-1920G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2687586 | ||||||
| chr4:2687696
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2332-1810G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2687696 | ||||||
| chr4:2687707
|
G | A | 1 | a0003c0003t0001g0235 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2332-1799G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2687707 | ||||||
| chr4:2687722
|
C | A | 93 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.2332-1784C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2687722 | ||||||
| chr4:2687727
|
C | T | 14 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(11): Show | 14 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2332-1779C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2687727 | ||||||
| chr4:2687729
|
T | C | 1 | a0005c0005t0002g0138 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2332-1777T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2687729 | ||||||
| chr4:2687896
|
C | G | 1 | a0001c0001t0002g0092 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2332-1610C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2687896 | ||||||
| chr4:2688016
|
A | G | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.2332-1490A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2688016 | ||||||
| chr4:2688095
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2332-1411T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2688095 | ||||||
| chr4:2688206
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2332-1300G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2688206 | ||||||
| chr4:2688436
|
G | A | 243 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.2332-1070G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2688436 | ||||||
| chr4:2688754
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2332-752G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2688754 | ||||||
| chr4:2689194
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2332-312C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2689194 | ||||||
| chr4:2689283
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0002g0010a0001c0001t0002g0062 | 3 | HG02080.hp1 HG02132.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.2332-223C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2689283 | ||||||
| chr4:2689304
|
T | G | 1 | a0007c0007t0003g0107 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2332-202T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | chr4 | 2689304 | ||||||
| chr4:2689438
|
G | GT | 25 | a0001c0001t0008g0215a0001c0002t0001g0001a0001c0002t0001g0002others(22): Show | 25 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.2332-65dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr4 | 2689438 | |||||
| chr4:2689824
|
C | G | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2530+120C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 14/20 | chr4 | 2689824 | ||||||
| chr4:2689927
|
TCCATGGC others(3): Show |
T | 1 | a0001c0002t0001g0113 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2530+226_2530+235d others(12): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr4 | 2689927 | |||||
| chr4:2689990
|
G | A | 1 | a0005c0005t0007g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2530+286G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 14/20 | chr4 | 2689990 | ||||||
| chr4:2690126
|
A | G | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2530+422A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 14/20 | chr4 | 2690126 | ||||||
| chr4:2690281
|
G | C | 1 | a0001c0002t0001g0001 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2531-417G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 14/20 | chr4 | 2690281 | ||||||
| chr4:2690488
|
G | A | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2531-210G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 14/20 | chr4 | 2690488 | ||||||
| chr4:2690977
|
C | T | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.2803+7C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2690977 | ||||||
| chr4:2690997
|
C | T | 3 | a0001c0001t0008g0215a0009c0010t0014g0228a0009c0010t0015g0229 | 3 | HG02486.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2803+27C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2690997 | ||||||
| chr4:2691002
|
T | A | 9 | a0002c0012t0004g0328a0005c0005t0004g0128a0005c0005t0004g0130others(6): Show | 9 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.2803+32T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2691002 | ||||||
| chr4:2691103
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0290 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2803+133C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2691103 | ||||||
| chr4:2691104
|
A | C | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.2803+134A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2691104 | ||||||
| chr4:2691266
|
A | C | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2803+296A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2691266 | ||||||
| chr4:2691327
|
T | C | 324 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.2803+357T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2691327 | ||||||
| chr4:2691413
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2803+443C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2691413 | ||||||
| chr4:2691510
|
C | G | 5 | a0001c0001t0001g0248a0001c0001t0001g0250a0001c0001t0001g0304others(2): Show | 5 | HG01071.hp2 HG02004.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2803+540C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2691510 | ||||||
| chr4:2691557
|
T | A | 3 | a0001c0002t0003g0112a0001c0002t0003g0120a0001c0002t0013g0117 | 3 | HG01516.hp1 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2803+587T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2691557 | ||||||
| chr4:2691768
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2803+798C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2691768 | ||||||
| chr4:2691774
|
T | TA | 172 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.2803+819dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 2691774 | |||||
| chr4:2691859
|
A | C | 1 | a0001c0001t0002g0039 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2803+889A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2691859 | ||||||
| chr4:2691951
|
A | G | 261 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.2803+981A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2691951 | ||||||
| chr4:2692011
|
A | G | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2803+1041A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2692011 | ||||||
| chr4:2692169
|
G | C | 77 | a0001c0001t0001g0122a0001c0001t0001g0243a0001c0001t0001g0244others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.2803+1199G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2692169 | ||||||
| chr4:2692213
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2803+1243C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2692213 | ||||||
| chr4:2692252
|
A | G | 39 | a0001c0001t0001g0122a0001c0001t0001g0176a0001c0001t0001g0223others(36): Show | 39 | HG01109.hp1 HG01891.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.2803+1282A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2692252 | ||||||
| chr4:2692269
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2803+1299G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2692269 | ||||||
| chr4:2692354
|
G | A | 37 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(34): Show | 37 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2804-1232G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2692354 | ||||||
| chr4:2692466
|
G | A | 1 | a0001c0001t0002g0048 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2804-1120G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2692466 | ||||||
| chr4:2692474
|
G | A | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2804-1112G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2692474 | ||||||
| chr4:2692658
|
A | G | 252 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.2804-928A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2692658 | ||||||
| chr4:2692689
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2804-897G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2692689 | ||||||
| chr4:2692756
|
A | C | 22 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(19): Show | 22 | HG00609.hp2 HG02145.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2804-830A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2692756 | ||||||
| chr4:2692845
|
AAGAG | A | 74 | a0001c0001t0001g0122a0001c0001t0001g0243a0001c0001t0001g0244others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.2804-736_2804-733d others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 2692845 | |||||
| chr4:2693046
|
G | C | 178 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.2804-540G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2693046 | ||||||
| chr4:2693050
|
AT | A | 26 | a0001c0001t0001g0250a0001c0001t0008g0215a0001c0021t0003g0143others(23): Show | 26 | HG00609.hp2 HG01891.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.2804-524delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 2693050 | |||||
| chr4:2693211
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2804-375G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2693211 | ||||||
| chr4:2693228
|
C | T | 2 | a0001c0001t0002g0024a0001c0001t0002g0025 | 2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.2804-358C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2693228 | ||||||
| chr4:2693313
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2804-273C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2693313 | ||||||
| chr4:2693331
|
TA | T | 22 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(19): Show | 22 | HG00609.hp2 HG02145.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.2804-249delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr4 | 2693331 | |||||
| chr4:2693390
|
T | C | 246 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.2804-196T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2693390 | ||||||
| chr4:2693406
|
G | A | 3 | a0001c0021t0003g0143a0004c0004t0001g0323a0004c0004t0001g0327 | 3 | HG02145.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2804-180G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2693406 | ||||||
| chr4:2693498
|
G | C | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2804-88G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 15/20 | chr4 | 2693498 | ||||||
| chr4:2693973
|
G | C | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3092+99G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 16/20 | chr4 | 2693973 | ||||||
| chr4:2694001
|
G | A | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3092+127G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 16/20 | chr4 | 2694001 | ||||||
| chr4:2694034
|
G | T | 5 | a0003c0003t0005g0164a0003c0003t0005g0187a0003c0003t0005g0188others(2): Show | 5 | HG02257.hp2 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.3092+160G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 16/20 | chr4 | 2694034 | ||||||
| chr4:2694393
|
C | T | 19 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(16): Show | 19 | HG00609.hp2 HG02145.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3092+519C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 16/20 | chr4 | 2694393 | ||||||
| chr4:2694441
|
G | A | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.3093-505G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 16/20 | chr4 | 2694441 | ||||||
| chr4:2694467
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3093-479C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 16/20 | chr4 | 2694467 | ||||||
| chr4:2694475
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3093-471G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 16/20 | chr4 | 2694475 | ||||||
| chr4:2694518
|
T | C | 247 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.3093-428T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 16/20 | chr4 | 2694518 | ||||||
| chr4:2694760
|
C | T | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3093-186C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 16/20 | chr4 | 2694760 | ||||||
| chr4:2694774
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3093-172C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 16/20 | chr4 | 2694774 | ||||||
| chr4:2694783
|
C | T | 248 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.3093-163C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 16/20 | chr4 | 2694783 | ||||||
| chr4:2694793
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3093-153G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 16/20 | chr4 | 2694793 | ||||||
| chr4:2694917
|
T | G | 1 | a0001c0001t0001g0218 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3093-29T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 16/20 | chr4 | 2694917 | ||||||
| chr4:2694919
|
C | G | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | NA18960.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.3093-27C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 16/20 | chr4 | 2694919 | ||||||
| chr4:2695362
|
A | C | 110 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.3276+233A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 17/20 | chr4 | 2695362 | ||||||
| chr4:2695429
|
G | A | 1 | a0001c0001t0002g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3276+300G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 17/20 | chr4 | 2695429 | ||||||
| chr4:2695457
|
G | T | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3276+328G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 17/20 | chr4 | 2695457 | ||||||
| chr4:2695567
|
T | C | 6 | a0001c0001t0001g0274a0001c0001t0001g0297a0001c0001t0001g0298others(3): Show | 6 | HG00673.hp1 HG02015.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.3276+438T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 17/20 | chr4 | 2695567 | ||||||
| chr4:2695573
|
A | G | 146 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(143): Show | 146 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.3276+444A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 17/20 | chr4 | 2695573 | ||||||
| chr4:2695842
|
G | C | 9 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(6): Show | 9 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.3277-521G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 17/20 | chr4 | 2695842 | ||||||
| chr4:2695969
|
A | G | 1 | a0001c0001t0002g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3277-394A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 17/20 | chr4 | 2695969 | ||||||
| chr4:2696029
|
A | AAAAT | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3277-310_3277-307d others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 2696029 | |||||
| chr4:2696029
|
A | AAAATAAA others(1): Show |
105 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.3277-314_3277-307d others(10): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 2696029 | |||||
| chr4:2696029
|
A | AAAATAAA others(5): Show |
3 | a0001c0001t0002g0009a0001c0001t0002g0017a0001c0001t0008g0215 | 3 | HG01074.hp2 HG02738.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3277-318_3277-307d others(14): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 2696029 | |||||
| chr4:2696067
|
C | G | 3 | a0001c0001t0001g0158a0001c0001t0001g0173a0001c0001t0001g0177 | 3 | HG00642.hp1 HG01192.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.3277-296C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 17/20 | chr4 | 2696067 | ||||||
| chr4:2696149
|
A | T | 1 | a0001c0001t0002g0093 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3277-214A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 17/20 | chr4 | 2696149 | ||||||
| chr4:2696637
|
C | T | 121 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0307others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.3507+44C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2696637 | ||||||
| chr4:2696695
|
G | T | 14 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(11): Show | 14 | HG01167.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.3507+102G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2696695 | ||||||
| chr4:2696704
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG03831.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3507+111G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2696704 | ||||||
| chr4:2696757
|
C | G | 1 | a0001c0001t0002g0035 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3507+164C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2696757 | ||||||
| chr4:2696797
|
G | A | 100 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0307others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.3507+204G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2696797 | ||||||
| chr4:2696913
|
G | A | 5 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(2): Show | 5 | HG01891.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3507+320G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2696913 | ||||||
| chr4:2697138
|
C | T | 121 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0307others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.3507+545C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2697138 | ||||||
| chr4:2697304
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3507+711C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2697304 | ||||||
| chr4:2697314
|
C | T | 120 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0307others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.3507+721C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2697314 | ||||||
| chr4:2697368
|
C | T | 1 | a0008c0009t0001g0310 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3507+775C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2697368 | ||||||
| chr4:2697533
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3507+940A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2697533 | ||||||
| chr4:2697880
|
G | C | 123 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0307others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.3507+1287G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2697880 | ||||||
| chr4:2697928
|
C | G | 109 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0307others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.3507+1335C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2697928 | ||||||
| chr4:2697955
|
C | T | 4 | a0004c0004t0001g0321a0004c0004t0003g0317a0004c0004t0003g0319others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.3507+1362C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2697955 | ||||||
| chr4:2698078
|
C | T | 1 | a0001c0001t0002g0048 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3507+1485C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2698078 | ||||||
| chr4:2698121
|
G | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0170a0001c0001t0001g0175 | 3 | HG02258.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3507+1528G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2698121 | ||||||
| chr4:2698173
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3508-1507C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2698173 | ||||||
| chr4:2698245
|
T | C | 246 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.3508-1435T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2698245 | ||||||
| chr4:2698346
|
C | A | 13 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.3508-1334C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2698346 | ||||||
| chr4:2698410
|
G | C | 9 | a0002c0012t0004g0328a0005c0005t0004g0128a0005c0005t0004g0130others(6): Show | 9 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.3508-1270G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2698410 | ||||||
| chr4:2698914
|
G | A | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3508-766G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2698914 | ||||||
| chr4:2699117
|
T | C | 236 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.3508-563T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2699117 | ||||||
| chr4:2699117
|
T | G | 10 | a0001c0001t0001g0264a0002c0012t0004g0328a0005c0005t0004g0128others(7): Show | 10 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.3508-563T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2699117 | ||||||
| chr4:2699291
|
A | T | 1 | a0001c0001t0002g0039 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3508-389A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2699291 | ||||||
| chr4:2699372
|
T | G | 113 | a0001c0001t0001g0122a0001c0001t0001g0152a0001c0001t0001g0231others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.3508-308T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2699372 | ||||||
| chr4:2699443
|
C | G | 1 | a0001c0001t0001g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3508-237C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2699443 | ||||||
| chr4:2699446
|
C | A | 5 | a0001c0001t0001g0263a0001c0001t0001g0290a0001c0001t0001g0306others(2): Show | 5 | HG00099.hp2 HG00741.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.3508-234C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2699446 | ||||||
| chr4:2699446
|
C | CCA | 54 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(51): Show | 54 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.3508-219_3508-218d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr4 | 2699446 | |||||
| chr4:2699446
|
C | CCCA | 16 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0256others(13): Show | 16 | HG00544.hp2 HG00735.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3508-233_3508-232i others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr4 | 2699446 | |||||
| chr4:2699446
|
CCA | C | 43 | a0001c0001t0001g0065a0001c0001t0002g0006a0001c0001t0002g0007others(40): Show | 43 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.3508-219_3508-218d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr4 | 2699446 | |||||
| chr4:2699447
|
CA | C | 32 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(29): Show | 32 | HG00140.hp1 HG00609.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.3508-232delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2699447 | ||||||
| chr4:2699447
|
CACA | C | 30 | a0001c0001t0001g0133a0001c0001t0002g0009a0001c0001t0002g0010others(27): Show | 30 | HG00099.hp1 HG00558.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.3508-232_3508-230d others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2699447 | ||||||
| chr4:2699448
|
A | C | 18 | a0001c0001t0001g0205a0001c0001t0001g0305a0001c0001t0002g0011others(15): Show | 18 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.3508-232A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2699448 | ||||||
| chr4:2699450
|
A | C | 76 | a0001c0001t0001g0065a0001c0001t0002g0006a0001c0001t0002g0007others(73): Show | 76 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.3508-230A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2699450 | ||||||
| chr4:2699452
|
A | C | 83 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.3508-228A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2699452 | ||||||
| chr4:2699454
|
A | C | 2 | a0001c0001t0002g0024a0001c0001t0002g0025 | 2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.3508-226A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2699454 | ||||||
| chr4:2699521
|
G | T | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3508-159G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2699521 | ||||||
| chr4:2699593
|
C | T | 9 | a0002c0012t0004g0328a0005c0005t0004g0128a0005c0005t0004g0130others(6): Show | 9 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.3508-87C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2699593 | ||||||
| chr4:2699672
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp2 | splice_region_variant&intron_variant | LOW | c.3508-8A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 18/20 | chr4 | 2699672 | ||||||
| chr4:2700582
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.4372+38G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2700582 | ||||||
| chr4:2700671
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4372+127C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2700671 | ||||||
| chr4:2700807
|
CA | C | 121 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.4372+272delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2700807 | |||||
| chr4:2700967
|
A | AAT | 8 | a0007c0007t0001g0110a0007c0007t0001g0115a0007c0007t0003g0106others(5): Show | 8 | HG01891.hp1 HG02717.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4372+425_4372+426d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2700967 | |||||
| chr4:2700971
|
C | T | 164 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(161): Show | 164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.4372+427C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2700971 | ||||||
| chr4:2700975
|
T | TAG | 14 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(11): Show | 14 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.4372+442_4372+443d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2700975 | |||||
| chr4:2700977
|
G | T | 10 | a0001c0001t0008g0215a0001c0021t0003g0143a0003c0003t0005g0187others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.4372+433G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2700977 | ||||||
| chr4:2701057
|
TTC | T | 121 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.4372+522_4372+523d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2701057 | |||||
| chr4:2701077
|
C | G | 155 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(152): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.4372+533C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2701077 | ||||||
| chr4:2701080
|
A | G | 99 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.4372+536A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2701080 | ||||||
| chr4:2701173
|
A | G | 1 | a0001c0001t0002g0035 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.4372+629A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2701173 | ||||||
| chr4:2701284
|
C | CA | 14 | a0001c0001t0001g0173a0001c0001t0001g0274a0001c0001t0001g0299others(11): Show | 14 | HG00099.hp1 HG00741.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.4372+757dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2701284 | |||||
| chr4:2701284
|
CA | C | 16 | a0001c0001t0001g0193a0001c0001t0001g0194a0003c0003t0001g0233others(13): Show | 16 | HG01891.hp2 HG02257.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.4372+757delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2701284 | |||||
| chr4:2701323
|
A | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4372+779A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2701323 | ||||||
| chr4:2701354
|
C | T | 107 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.4372+810C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2701354 | ||||||
| chr4:2701374
|
T | G | 77 | a0001c0001t0001g0122a0001c0001t0001g0241a0001c0001t0001g0243others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.4372+830T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2701374 | ||||||
| chr4:2701459
|
G | T | 4 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0085others(1): Show | 4 | HG00323.hp2 HG01099.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.4372+915G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2701459 | ||||||
| chr4:2701559
|
T | G | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4372+1015T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2701559 | ||||||
| chr4:2701562
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4372+1018C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2701562 | ||||||
| chr4:2701602
|
G | C | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.4372+1058G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2701602 | ||||||
| chr4:2701745
|
C | T | 1 | a0009c0010t0014g0228 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4372+1201C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2701745 | ||||||
| chr4:2701778
|
A | AT | 30 | a0001c0001t0001g0241a0001c0001t0001g0263a0001c0001t0001g0290others(27): Show | 30 | HG00741.hp2 HG01175.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.4372+1249dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2701778 | |||||
| chr4:2701824
|
T | G | 1 | a0001c0001t0012g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4372+1280T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2701824 | ||||||
| chr4:2702015
|
G | A | 1 | a0001c0001t0004g0208 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4372+1471G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2702015 | ||||||
| chr4:2702090
|
A | G | 1 | a0003c0003t0005g0187 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4372+1546A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2702090 | ||||||
| chr4:2702135
|
G | A | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.4372+1591G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2702135 | ||||||
| chr4:2702268
|
C | T | 9 | a0003c0003t0004g0155a0003c0003t0005g0164a0003c0003t0005g0187others(6): Show | 9 | HG02257.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.4372+1724C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2702268 | ||||||
| chr4:2702319
|
G | A | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.4372+1775G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2702319 | ||||||
| chr4:2702362
|
C | T | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4372+1818C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2702362 | ||||||
| chr4:2702699
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4372+2155C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2702699 | ||||||
| chr4:2702894
|
C | T | 124 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.4372+2350C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2702894 | ||||||
| chr4:2702901
|
G | C | 124 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.4372+2357G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2702901 | ||||||
| chr4:2702922
|
C | T | 2 | a0002c0014t0001g0270a0008c0009t0001g0295 | 2 | NA18947.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.4372+2378C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2702922 | ||||||
| chr4:2702992
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.4372+2448C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2702992 | ||||||
| chr4:2703182
|
C | T | 6 | a0001c0001t0001g0122a0001c0001t0001g0248a0001c0001t0001g0250others(3): Show | 6 | HG02004.hp2 HG02523.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.4372+2638C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2703182 | ||||||
| chr4:2703183
|
G | T | 123 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.4372+2639G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2703183 | ||||||
| chr4:2703257
|
T | G | 1 | a0001c0001t0001g0178 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4372+2713T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2703257 | ||||||
| chr4:2703365
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0160a0001c0001t0001g0174 | 3 | NA18947.hp1 NA19010.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.4372+2821G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2703365 | ||||||
| chr4:2703644
|
T | C | 4 | a0004c0004t0001g0321a0004c0004t0003g0317a0004c0004t0003g0319others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4372+3100T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2703644 | ||||||
| chr4:2703722
|
G | T | 9 | a0002c0012t0004g0328a0005c0005t0004g0128a0005c0005t0004g0130others(6): Show | 9 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.4372+3178G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2703722 | ||||||
| chr4:2703801
|
T | TA | 7 | a0001c0001t0001g0152a0001c0001t0001g0217a0001c0001t0001g0231others(4): Show | 7 | HG00741.hp2 HG01516.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.4372+3273dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2703801 | |||||
| chr4:2703801
|
T | TAA | 119 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(116): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.4372+3272_4372+327 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2703801 | |||||
| chr4:2703801
|
TA | T | 45 | a0001c0001t0001g0293a0001c0002t0001g0001a0001c0002t0001g0002others(42): Show | 45 | HG00408.hp1 HG01074.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.4372+3273delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2703801 | |||||
| chr4:2703911
|
G | T | 10 | a0002c0012t0004g0328a0005c0005t0004g0128a0005c0005t0004g0130others(7): Show | 10 | HG00408.hp1 HG01074.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.4372+3367G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2703911 | ||||||
| chr4:2703917
|
T | A | 124 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.4372+3373T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2703917 | ||||||
| chr4:2704124
|
G | A | 1 | a0001c0001t0002g0329 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4372+3580G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2704124 | ||||||
| chr4:2704192
|
G | A | 1 | a0005c0005t0002g0138 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4372+3648G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2704192 | ||||||
| chr4:2704204
|
A | G | 1 | a0001c0001t0002g0034 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4372+3660A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2704204 | ||||||
| chr4:2704214
|
G | A | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.4372+3670G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2704214 | ||||||
| chr4:2704261
|
C | CA | 79 | a0001c0001t0001g0163a0001c0001t0001g0243a0001c0001t0001g0244others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.4372+3735dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2704261 | |||||
| chr4:2704302
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4372+3758A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2704302 | ||||||
| chr4:2704313
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4372+3769C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2704313 | ||||||
| chr4:2704376
|
A | G | 171 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0152others(168): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.4372+3832A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2704376 | ||||||
| chr4:2704529
|
CA | C | 12 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.4372+3986delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2704529 | ||||||
| chr4:2704574
|
T | A | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.4372+4030T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2704574 | ||||||
| chr4:2704578
|
A | G | 1 | a0002c0012t0004g0328 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.4372+4034A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2704578 | ||||||
| chr4:2704584
|
A | G | 3 | a0001c0001t0002g0036a0001c0001t0002g0067a0001c0001t0002g0068 | 3 | HG01070.hp2 HG01071.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.4372+4040A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2704584 | ||||||
| chr4:2704742
|
G | A | 1 | a0001c0001t0012g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4372+4198G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2704742 | ||||||
| chr4:2704814
|
T | A | 1 | a0001c0001t0001g0241 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.4372+4270T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2704814 | ||||||
| chr4:2704887
|
T | C | 1 | a0001c0001t0001g0303 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.4372+4343T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2704887 | ||||||
| chr4:2704913
|
A | ATTTTGTT others(5): Show |
14 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(11): Show | 14 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.4372+4375_4372+438 others(16): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2704913 | |||||
| chr4:2704972
|
C | T | 10 | a0002c0012t0004g0328a0005c0005t0004g0128a0005c0005t0004g0130others(7): Show | 10 | HG00408.hp1 HG01074.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.4372+4428C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2704972 | ||||||
| chr4:2705012
|
C | T | 122 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.4372+4468C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2705012 | ||||||
| chr4:2705222
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4372+4678A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2705222 | ||||||
| chr4:2705305
|
G | A | 66 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(63): Show | 66 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.4372+4761G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2705305 | ||||||
| chr4:2705385
|
T | C | 1 | a0006c0008t0001g0121 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4372+4841T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2705385 | ||||||
| chr4:2705405
|
G | A | 123 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.4372+4861G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2705405 | ||||||
| chr4:2705464
|
C | CT | 124 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0158others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.4372+4929dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2705464 | |||||
| chr4:2705491
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4372+4947T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2705491 | ||||||
| chr4:2705499
|
A | C | 1 | a0002c0006t0001g0242 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4372+4955A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2705499 | ||||||
| chr4:2705525
|
A | T | 1 | a0001c0001t0002g0048 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.4372+4981A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2705525 | ||||||
| chr4:2705550
|
A | T | 1 | a0001c0001t0001g0241 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.4372+5006A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2705550 | ||||||
| chr4:2705551
|
T | G | 1 | a0001c0001t0001g0241 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.4372+5007T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2705551 | ||||||
| chr4:2705598
|
T | G | 120 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.4372+5054T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2705598 | ||||||
| chr4:2705601
|
G | A | 1 | a0006c0008t0001g0132 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4372+5057G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2705601 | ||||||
| chr4:2705652
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4372+5108C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2705652 | ||||||
| chr4:2705697
|
C | A | 1 | a0005c0005t0004g0135 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4372+5153C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2705697 | ||||||
| chr4:2705755
|
AT | A | 121 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.4372+5224delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2705755 | |||||
| chr4:2705787
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4372+5243C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2705787 | ||||||
| chr4:2705861
|
C | T | 167 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(164): Show | 167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.4372+5317C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2705861 | ||||||
| chr4:2706055
|
T | A | 1 | a0001c0001t0001g0199 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4372+5511T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2706055 | ||||||
| chr4:2706150
|
A | G | 1 | a0006c0008t0001g0125 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4372+5606A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2706150 | ||||||
| chr4:2706162
|
T | A | 10 | a0002c0012t0004g0328a0005c0005t0004g0128a0005c0005t0004g0130others(7): Show | 10 | HG00408.hp1 HG01074.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.4372+5618T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2706162 | ||||||
| chr4:2706171
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4372+5627G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2706171 | ||||||
| chr4:2706287
|
C | T | 1 | a0006c0008t0001g0121 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4372+5743C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2706287 | ||||||
| chr4:2706291
|
C | CT | 31 | a0001c0001t0001g0144a0001c0001t0001g0162a0001c0001t0002g0014others(28): Show | 31 | HG00140.hp1 HG00738.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.4372+5769dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2706291 | |||||
| chr4:2706291
|
C | CTT | 98 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(95): Show | 98 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.4372+5768_4372+576 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2706291 | |||||
| chr4:2706291
|
C | CTTT | 11 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0020others(8): Show | 11 | HG00642.hp2 HG01175.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.4372+5767_4372+576 others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2706291 | |||||
| chr4:2706291
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.4372+5747C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2706291 | ||||||
| chr4:2706291
|
CT | C | 13 | a0001c0001t0001g0004a0001c0001t0001g0206a0001c0001t0001g0211others(10): Show | 13 | HG01070.hp1 HG01167.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.4372+5769delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2706291 | |||||
| chr4:2706295
|
T | C | 84 | a0001c0001t0001g0122a0001c0001t0001g0152a0001c0001t0001g0231others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.4372+5751T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2706295 | ||||||
| chr4:2706296
|
T | C | 5 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0277others(2): Show | 5 | HG01070.hp1 HG01167.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.4372+5752T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2706296 | ||||||
| chr4:2706299
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4372+5755T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2706299 | ||||||
| chr4:2706341
|
G | A | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4372+5797G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2706341 | ||||||
| chr4:2706432
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.4372+5888G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2706432 | ||||||
| chr4:2706433
|
A | T | 1 | a0001c0001t0001g0241 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.4372+5889A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2706433 | ||||||
| chr4:2706542
|
C | T | 1 | a0006c0008t0001g0216 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4372+5998C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2706542 | ||||||
| chr4:2706591
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.4372+6047C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2706591 | ||||||
| chr4:2706683
|
TTTAG | T | 14 | a0001c0001t0001g0263a0001c0001t0001g0290a0003c0003t0001g0233others(11): Show | 14 | HG01516.hp2 HG01517.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.4372+6147_4372+615 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2706683 | |||||
| chr4:2706817
|
G | T | 5 | a0001c0001t0002g0057a0001c0001t0002g0076a0001c0001t0002g0077others(2): Show | 5 | HG00733.hp2 HG01358.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.4372+6273G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2706817 | ||||||
| chr4:2706911
|
A | C | 1 | a0001c0001t0002g0048 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.4372+6367A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2706911 | ||||||
| chr4:2706915
|
GT | G | 76 | a0001c0001t0001g0122a0001c0001t0001g0243a0001c0001t0001g0244others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.4372+6373delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2706915 | |||||
| chr4:2707087
|
G | A | 157 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(154): Show | 157 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.4372+6543G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2707087 | ||||||
| chr4:2707095
|
C | T | 5 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(2): Show | 5 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.4372+6551C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2707095 | ||||||
| chr4:2707102
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4372+6558A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2707102 | ||||||
| chr4:2707125
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4372+6581C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2707125 | ||||||
| chr4:2707349
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4372+6805A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2707349 | ||||||
| chr4:2707435
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4372+6891A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2707435 | ||||||
| chr4:2707626
|
G | A | 1 | a0002c0011t0003g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4372+7082G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2707626 | ||||||
| chr4:2707713
|
A | AT | 81 | a0001c0001t0001g0193a0001c0001t0001g0201a0001c0001t0001g0209others(78): Show | 81 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.4372+7186dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2707713 | |||||
| chr4:2707713
|
A | ATT | 8 | a0001c0001t0001g0122a0001c0001t0001g0253a0001c0001t0001g0254others(5): Show | 8 | HG00140.hp2 HG00735.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.4372+7185_4372+718 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2707713 | |||||
| chr4:2707713
|
AT | A | 9 | a0001c0001t0007g0129a0007c0007t0001g0110a0007c0007t0001g0115others(6): Show | 9 | HG01167.hp2 HG01891.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.4372+7186delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2707713 | |||||
| chr4:2707808
|
C | T | 12 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(9): Show | 12 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.4372+7264C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2707808 | ||||||
| chr4:2707879
|
G | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0273 | 2 | HG00733.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.4372+7335G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2707879 | ||||||
| chr4:2708133
|
T | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4372+7589T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2708133 | ||||||
| chr4:2708143
|
G | A | 1 | a0001c0002t0003g0120 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4372+7599G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2708143 | ||||||
| chr4:2708213
|
C | T | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.4372+7669C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2708213 | ||||||
| chr4:2708242
|
C | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0020a0001c0001t0002g0021others(2): Show | 5 | HG01106.hp1 HG02886.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.4372+7698C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2708242 | ||||||
| chr4:2708292
|
A | G | 1 | a0005c0005t0004g0135 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4373-7731A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2708292 | ||||||
| chr4:2708329
|
T | C | 1 | a0001c0001t0002g0033 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.4373-7694T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2708329 | ||||||
| chr4:2708364
|
ATCCACCC others(20): Show |
A | 1 | a0001c0001t0001g0241 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.4373-7657_4373-763 others(31): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2708364 | |||||
| chr4:2708377
|
G | A | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0329 | 3 | HG01106.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4373-7646G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2708377 | ||||||
| chr4:2708420
|
C | T | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.4373-7603C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2708420 | ||||||
| chr4:2708525
|
C | T | 121 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.4373-7498C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2708525 | ||||||
| chr4:2708579
|
C | T | 5 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(2): Show | 5 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(2): Show |
intron_variant | MODIFIER | c.4373-7444C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2708579 | ||||||
| chr4:2708706
|
G | C | 7 | a0001c0001t0002g0035a0001c0001t0002g0039a0001c0001t0002g0053others(4): Show | 7 | NA18612.hp2 NA18942.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.4373-7317G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2708706 | ||||||
| chr4:2708753
|
C | T | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4373-7270C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2708753 | ||||||
| chr4:2708791
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4373-7232T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2708791 | ||||||
| chr4:2708894
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4373-7129A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2708894 | ||||||
| chr4:2708898
|
C | G | 2 | a0001c0001t0001g0150a0001c0001t0010g0149 | 2 | HG00639.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.4373-7125C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2708898 | ||||||
| chr4:2708904
|
C | T | 1 | a0001c0001t0002g0007 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.4373-7119C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2708904 | ||||||
| chr4:2708917
|
T | G | 76 | a0001c0001t0001g0122a0001c0001t0001g0243a0001c0001t0001g0244others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.4373-7106T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2708917 | ||||||
| chr4:2709124
|
G | A | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4373-6899G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2709124 | ||||||
| chr4:2709219
|
G | A | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4373-6804G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2709219 | ||||||
| chr4:2709235
|
G | C | 121 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.4373-6788G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2709235 | ||||||
| chr4:2709435
|
C | T | 121 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.4373-6588C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2709435 | ||||||
| chr4:2709450
|
A | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4373-6573A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2709450 | ||||||
| chr4:2709580
|
G | A | 1 | a0002c0006t0001g0287 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4373-6443G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2709580 | ||||||
| chr4:2709602
|
A | G | 261 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.4373-6421A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2709602 | ||||||
| chr4:2709666
|
GC | G | 5 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(2): Show | 5 | HG01891.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4373-6355delC | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2709666 | |||||
| chr4:2709705
|
A | AAAAAC | 13 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.4373-6296_4373-629 others(9): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2709705 | |||||
| chr4:2709705
|
AAAAAC | A | 3 | a0004c0004t0001g0325a0004c0004t0001g0326a0005c0005t0004g0134 | 3 | HG00408.hp1 HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4373-6296_4373-629 others(9): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2709705 | |||||
| chr4:2709746
|
G | GT | 13 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.4373-6271dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2709746 | |||||
| chr4:2709781
|
A | G | 1 | a0005c0005t0004g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4373-6242A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2709781 | ||||||
| chr4:2709792
|
C | G | 9 | a0002c0012t0004g0328a0005c0005t0004g0128a0005c0005t0004g0130others(6): Show | 9 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.4373-6231C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2709792 | ||||||
| chr4:2710043
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.4373-5980A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710043 | ||||||
| chr4:2710161
|
G | GT | 8 | a0001c0001t0001g0262a0001c0001t0001g0284a0001c0001t0001g0302others(5): Show | 8 | HG00408.hp1 HG00735.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.4373-5847dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2710161 | |||||
| chr4:2710161
|
G | GTT | 10 | a0001c0001t0001g0065a0001c0001t0001g0312a0001c0001t0001g0313others(7): Show | 10 | HG01074.hp1 HG01934.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.4373-5848_4373-584 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2710161 | |||||
| chr4:2710161
|
G | T | 3 | a0001c0001t0002g0071a0006c0008t0001g0125a0006c0008t0001g0126 | 3 | HG02559.hp2 NA18974.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4373-5862G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710161 | ||||||
| chr4:2710161
|
GT | G | 67 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0145others(64): Show | 67 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.4373-5847delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2710161 | |||||
| chr4:2710162
|
TTTTTTTT others(8): Show |
T | 16 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(13): Show | 16 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.4373-5846_4373-583 others(19): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2710162 | |||||
| chr4:2710163
|
TTTTTTTT others(7): Show |
T | 6 | a0001c0002t0001g0240a0001c0002t0003g0116a0001c0002t0003g0119others(3): Show | 6 | HG02055.hp2 HG02970.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.4373-5846_4373-583 others(18): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2710163 | |||||
| chr4:2710166
|
T | TG | 3 | a0001c0001t0001g0152a0001c0001t0001g0231a0001c0001t0001g0232 | 3 | HG02647.hp1 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4373-5857_4373-585 others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710166 | ||||||
| chr4:2710167
|
T | G | 1 | a0001c0001t0001g0298 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4373-5856T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710167 | ||||||
| chr4:2710168
|
T | G | 1 | a0001c0001t0002g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4373-5855T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710168 | ||||||
| chr4:2710176
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.4373-5847T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710176 | ||||||
| chr4:2710177
|
C | T | 119 | a0001c0001t0001g0123a0001c0001t0001g0241a0001c0001t0002g0006others(116): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.4373-5846C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710177 | ||||||
| chr4:2710178
|
T | C | 104 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.4373-5845T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710178 | ||||||
| chr4:2710178
|
T | TC | 12 | a0001c0001t0001g0241a0001c0001t0002g0011a0001c0001t0002g0015others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.4373-5845_4373-584 others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710178 | ||||||
| chr4:2710213
|
C | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4373-5810C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710213 | ||||||
| chr4:2710225
|
C | A | 246 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.4373-5798C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710225 | ||||||
| chr4:2710235
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4373-5788C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710235 | ||||||
| chr4:2710279
|
A | G | 16 | a0001c0001t0001g0241a0001c0001t0002g0035a0001c0001t0002g0039others(13): Show | 16 | HG01928.hp1 HG02004.hp1 NA18612.hp2 others(13): Show |
intron_variant | MODIFIER | c.4373-5744A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710279 | ||||||
| chr4:2710348
|
T | C | 120 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.4373-5675T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710348 | ||||||
| chr4:2710395
|
C | G | 156 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(153): Show | 156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.4373-5628C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710395 | ||||||
| chr4:2710621
|
C | A | 13 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.4373-5402C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710621 | ||||||
| chr4:2710676
|
T | C | 123 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.4373-5347T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710676 | ||||||
| chr4:2710686
|
G | C | 2 | a0001c0001t0002g0024a0001c0001t0002g0025 | 2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.4373-5337G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710686 | ||||||
| chr4:2710851
|
C | CT | 86 | a0001c0001t0001g0122a0001c0001t0001g0157a0001c0001t0001g0168others(83): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.4373-5154dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2710851 | |||||
| chr4:2710851
|
CT | C | 116 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.4373-5154delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2710851 | |||||
| chr4:2710961
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4373-5062C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710961 | ||||||
| chr4:2710989
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0213 | 2 | NA18982.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.4373-5034C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710989 | ||||||
| chr4:2710996
|
C | T | 1 | a0008c0009t0001g0295 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.4373-5027C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2710996 | ||||||
| chr4:2711007
|
T | A | 1 | a0001c0001t0002g0033 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.4373-5016T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2711007 | ||||||
| chr4:2711008
|
C | T | 2 | a0001c0001t0001g0274a0003c0003t0004g0155 | 2 | HG02083.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.4373-5015C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2711008 | ||||||
| chr4:2711019
|
T | C | 3 | a0001c0001t0001g0255a0001c0001t0001g0259a0002c0006t0001g0242 | 3 | HG02055.hp1 HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.4373-5004T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2711019 | ||||||
| chr4:2711054
|
A | G | 109 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.4373-4969A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2711054 | ||||||
| chr4:2711068
|
G | A | 3 | a0001c0021t0003g0143a0004c0004t0001g0323a0004c0004t0001g0327 | 3 | HG02145.hp1 HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4373-4955G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2711068 | ||||||
| chr4:2711169
|
T | A | 1 | a0001c0001t0002g0011 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.4373-4854T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2711169 | ||||||
| chr4:2711262
|
G | T | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4373-4761G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2711262 | ||||||
| chr4:2711277
|
G | C | 197 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.4373-4746G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2711277 | ||||||
| chr4:2711280
|
C | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4373-4743C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2711280 | ||||||
| chr4:2711438
|
C | G | 1 | a0013c0019t0002g0055 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4373-4585C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2711438 | ||||||
| chr4:2711550
|
G | A | 3 | a0001c0001t0002g0011a0001c0001t0002g0040a0001c0001t0002g0047 | 3 | NA18967.hp1 NA19007.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.4373-4473G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2711550 | ||||||
| chr4:2711619
|
C | T | 1 | a0001c0001t0012g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4373-4404C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2711619 | ||||||
| chr4:2711661
|
A | G | 1 | a0001c0001t0001g0251 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4373-4362A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2711661 | ||||||
| chr4:2711788
|
G | A | 76 | a0001c0001t0001g0122a0001c0001t0001g0243a0001c0001t0001g0244others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.4373-4235G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2711788 | ||||||
| chr4:2712019
|
T | C | 1 | a0004c0004t0001g0322 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4373-4004T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2712019 | ||||||
| chr4:2712181
|
G | A | 1 | a0002c0012t0004g0328 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.4373-3842G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2712181 | ||||||
| chr4:2712296
|
T | C | 121 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.4373-3727T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2712296 | ||||||
| chr4:2712384
|
C | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.4373-3639C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2712384 | ||||||
| chr4:2712407
|
G | C | 8 | a0007c0007t0001g0110a0007c0007t0001g0115a0007c0007t0003g0106others(5): Show | 8 | HG01891.hp1 HG02717.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.4373-3616G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2712407 | ||||||
| chr4:2712442
|
C | G | 76 | a0001c0001t0001g0122a0001c0001t0001g0243a0001c0001t0001g0244others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.4373-3581C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2712442 | ||||||
| chr4:2712505
|
C | T | 4 | a0004c0004t0001g0321a0004c0004t0003g0317a0004c0004t0003g0319others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4373-3518C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2712505 | ||||||
| chr4:2712595
|
G | T | 1 | a0005c0005t0004g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4373-3428G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2712595 | ||||||
| chr4:2712698
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.4373-3325G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2712698 | ||||||
| chr4:2712755
|
T | C | 122 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0241others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.4373-3268T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2712755 | ||||||
| chr4:2713083
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4373-2940C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2713083 | ||||||
| chr4:2713104
|
C | CA | 18 | a0001c0001t0001g0122a0001c0001t0001g0171a0001c0001t0001g0202others(15): Show | 18 | HG01891.hp1 HG02135.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.4373-2901dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2713104 | |||||
| chr4:2713104
|
C | CAA | 6 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.4373-2902_4373-290 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2713104 | |||||
| chr4:2713104
|
CA | C | 6 | a0001c0001t0002g0073a0001c0001t0002g0079a0001c0001t0002g0093others(3): Show | 6 | HG02257.hp1 HG03471.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.4373-2901delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr4 | 2713104 | |||||
| chr4:2713298
|
C | T | 15 | a0001c0001t0001g0250a0003c0003t0001g0233a0003c0003t0001g0234others(12): Show | 15 | HG01891.hp2 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.4373-2725C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2713298 | ||||||
| chr4:2713411
|
C | G | 11 | a0001c0001t0001g0219a0002c0012t0004g0328a0005c0005t0004g0128others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.4373-2612C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2713411 | ||||||
| chr4:2714031
|
G | A | 121 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.4373-1992G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2714031 | ||||||
| chr4:2714176
|
A | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4373-1847A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2714176 | ||||||
| chr4:2714294
|
C | A | 1 | a0001c0001t0002g0017 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4373-1729C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2714294 | ||||||
| chr4:2714339
|
G | T | 1 | a0001c0016t0001g0308 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4373-1684G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2714339 | ||||||
| chr4:2714360
|
T | C | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4373-1663T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2714360 | ||||||
| chr4:2714420
|
A | C | 121 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.4373-1603A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2714420 | ||||||
| chr4:2714558
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4373-1465C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2714558 | ||||||
| chr4:2714977
|
C | T | 9 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(6): Show | 9 | HG02145.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.4373-1046C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2714977 | ||||||
| chr4:2715252
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.4373-771C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2715252 | ||||||
| chr4:2715273
|
G | C | 1 | a0001c0001t0001g0297 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4373-750G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2715273 | ||||||
| chr4:2715563
|
A | G | 4 | a0004c0004t0001g0321a0004c0004t0003g0317a0004c0004t0003g0319others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4373-460A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2715563 | ||||||
| chr4:2715600
|
T | C | 261 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.4373-423T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2715600 | ||||||
| chr4:2715642
|
C | G | 1 | a0001c0001t0002g0013 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4373-381C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2715642 | ||||||
| chr4:2715681
|
A | G | 10 | a0002c0012t0004g0328a0005c0005t0002g0138a0005c0005t0004g0128others(7): Show | 10 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.4373-342A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2715681 | ||||||
| chr4:2715788
|
G | A | 120 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.4373-235G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2715788 | ||||||
| chr4:2715802
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4373-221C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2715802 | ||||||
| chr4:2715919
|
A | G | 1 | a0005c0005t0004g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4373-104A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2715919 | ||||||
| chr4:2715963
|
C | T | 144 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.4373-60C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 19/20 | chr4 | 2715963 | ||||||
| chr4:2716113
|
G | A | 3 | a0001c0002t0003g0112a0001c0002t0003g0120a0001c0002t0013g0117 | 3 | HG01516.hp1 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.4454+9G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2716113 | ||||||
| chr4:2716287
|
C | T | 1 | a0001c0021t0003g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4454+183C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2716287 | ||||||
| chr4:2716436
|
G | C | 12 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(9): Show | 12 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.4454+332G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2716436 | ||||||
| chr4:2716462
|
G | T | 1 | a0001c0018t0001g0260 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4454+358G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2716462 | ||||||
| chr4:2716497
|
G | A | 1 | a0007c0007t0003g0109 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4454+393G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2716497 | ||||||
| chr4:2716721
|
G | T | 2 | a0001c0001t0001g0150a0001c0001t0010g0149 | 2 | HG00639.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.4454+617G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2716721 | ||||||
| chr4:2716875
|
C | T | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4454+771C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2716875 | ||||||
| chr4:2716906
|
C | G | 1 | a0001c0001t0002g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4454+802C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2716906 | ||||||
| chr4:2716987
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4454+883T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2716987 | ||||||
| chr4:2717068
|
C | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4454+964C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2717068 | ||||||
| chr4:2717136
|
C | T | 5 | a0002c0012t0004g0328a0005c0005t0004g0128a0005c0005t0004g0135others(2): Show | 5 | HG01074.hp1 HG03654.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.4454+1032C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2717136 | ||||||
| chr4:2717172
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.4454+1068G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2717172 | ||||||
| chr4:2717331
|
A | G | 123 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.4454+1227A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2717331 | ||||||
| chr4:2717577
|
CAGAG | C | 10 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(7): Show | 10 | HG02145.hp1 HG02258.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.4454+1479_4454+148 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2717577 | |||||
| chr4:2717598
|
G | GA | 136 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0122others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.4454+1511dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2717598 | |||||
| chr4:2717598
|
G | GAA | 11 | a0001c0001t0001g0213a0001c0001t0002g0009a0001c0001t0002g0011others(8): Show | 11 | HG01175.hp2 HG01358.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.4454+1510_4454+151 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2717598 | |||||
| chr4:2717754
|
G | GA | 13 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0169others(10): Show | 13 | HG02135.hp2 HG02145.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.4454+1668dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2717754 | |||||
| chr4:2717754
|
GA | G | 30 | a0001c0001t0001g0302a0001c0001t0001g0312a0001c0001t0001g0313others(27): Show | 30 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.4454+1668delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2717754 | |||||
| chr4:2717754
|
GAA | G | 136 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0007others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.4454+1667_4454+166 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2717754 | |||||
| chr4:2717811
|
G | A | 75 | a0001c0001t0001g0122a0001c0001t0001g0241a0001c0001t0001g0243others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.4454+1707G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2717811 | ||||||
| chr4:2717994
|
A | G | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4454+1890A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2717994 | ||||||
| chr4:2718052
|
T | G | 1 | a0001c0001t0002g0094 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4454+1948T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2718052 | ||||||
| chr4:2718252
|
C | G | 1 | a0007c0007t0003g0118 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4454+2148C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2718252 | ||||||
| chr4:2718350
|
C | T | 245 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.4454+2246C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2718350 | ||||||
| chr4:2718426
|
TA | T | 163 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.4454+2335delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2718426 | |||||
| chr4:2718437
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4454+2333A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2718437 | ||||||
| chr4:2718464
|
T | C | 1 | a0005c0005t0004g0135 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4454+2360T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2718464 | ||||||
| chr4:2718496
|
A | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4454+2392A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2718496 | ||||||
| chr4:2718699
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.4454+2595C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2718699 | ||||||
| chr4:2718708
|
C | T | 9 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(6): Show | 9 | HG02145.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.4454+2604C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2718708 | ||||||
| chr4:2718858
|
A | C | 1 | a0001c0001t0001g0276 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.4454+2754A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2718858 | ||||||
| chr4:2719063
|
G | A | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4454+2959G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2719063 | ||||||
| chr4:2719154
|
G | T | 2 | a0001c0001t0002g0017a0001c0001t0002g0091 | 2 | HG01074.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.4454+3050G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2719154 | ||||||
| chr4:2719405
|
G | C | 159 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(156): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.4454+3301G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2719405 | ||||||
| chr4:2719472
|
G | A | 120 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.4454+3368G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2719472 | ||||||
| chr4:2719512
|
C | G | 144 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.4454+3408C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2719512 | ||||||
| chr4:2719529
|
T | C | 2 | a0008c0009t0001g0266a0008c0009t0001g0301 | 2 | NA18944.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.4454+3425T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2719529 | ||||||
| chr4:2719641
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4454+3537A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2719641 | ||||||
| chr4:2719721
|
G | A | 1 | a0001c0001t0004g0208 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4454+3617G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2719721 | ||||||
| chr4:2719740
|
C | CA | 155 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0171others(152): Show | 155 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.4454+3654dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2719740 | |||||
| chr4:2719740
|
C | CAA | 12 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0012others(9): Show | 12 | HG01175.hp2 HG01891.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.4454+3653_4454+365 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2719740 | |||||
| chr4:2719770
|
T | C | 27 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(24): Show | 27 | HG00408.hp1 HG01074.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.4454+3666T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2719770 | ||||||
| chr4:2719770
|
T | TCCTC | 18 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0008g0215others(15): Show | 18 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.4454+3690_4454+369 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2719770 | |||||
| chr4:2719770
|
TCCTCCCT others(5): Show |
T | 108 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.4454+3682_4454+369 others(16): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2719770 | |||||
| chr4:2719772
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.4454+3668C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2719772 | ||||||
| chr4:2719784
|
C | T | 1 | a0005c0005t0004g0140 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4454+3680C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2719784 | ||||||
| chr4:2719798
|
T | C | 4 | a0004c0004t0001g0325a0004c0004t0001g0326a0009c0010t0014g0228others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4454+3694T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2719798 | ||||||
| chr4:2719803
|
C | T | 119 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(116): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.4454+3699C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2719803 | ||||||
| chr4:2719943
|
C | T | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.4454+3839C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2719943 | ||||||
| chr4:2719955
|
A | G | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.4454+3851A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2719955 | ||||||
| chr4:2720032
|
T | C | 10 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0259others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.4454+3928T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2720032 | ||||||
| chr4:2720084
|
C | T | 77 | a0001c0001t0001g0122a0001c0001t0001g0241a0001c0001t0001g0243others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.4454+3980C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2720084 | ||||||
| chr4:2720647
|
T | TA | 17 | a0001c0001t0001g0162a0001c0001t0001g0166a0001c0001t0002g0071others(14): Show | 17 | HG01175.hp1 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.4454+4560dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2720647 | |||||
| chr4:2720647
|
TA | T | 74 | a0001c0001t0001g0122a0001c0001t0001g0241a0001c0001t0001g0244others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.4454+4560delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2720647 | |||||
| chr4:2721027
|
G | T | 5 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(2): Show | 5 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.4454+4923G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2721027 | ||||||
| chr4:2721039
|
C | T | 2 | a0001c0001t0002g0035a0001c0001t0002g0087 | 2 | NA18942.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.4454+4935C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2721039 | ||||||
| chr4:2721066
|
C | T | 120 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.4454+4962C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2721066 | ||||||
| chr4:2721088
|
T | C | 158 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(155): Show | 158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.4454+4984T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2721088 | ||||||
| chr4:2721095
|
C | T | 7 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0066others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.4454+4991C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2721095 | ||||||
| chr4:2721267
|
T | G | 1 | a0001c0001t0001g0213 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.4454+5163T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2721267 | ||||||
| chr4:2721312
|
C | CA | 21 | a0001c0001t0001g0147a0001c0001t0001g0151a0001c0001t0001g0153others(18): Show | 21 | HG01081.hp2 HG01167.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.4454+5237dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2721312 | |||||
| chr4:2721312
|
C | CAA | 8 | a0001c0001t0001g0152a0001c0001t0001g0174a0001c0001t0001g0178others(5): Show | 8 | HG00544.hp1 HG01978.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.4454+5236_4454+523 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2721312 | |||||
| chr4:2721312
|
CAAA | C | 23 | a0001c0001t0001g0243a0001c0001t0001g0254a0001c0001t0001g0258others(20): Show | 23 | HG00673.hp1 HG00735.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.4454+5235_4454+523 others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2721312 | |||||
| chr4:2721312
|
CAAAA | C | 83 | a0001c0001t0001g0122a0001c0001t0001g0241a0001c0001t0001g0244others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.4454+5234_4454+523 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2721312 | |||||
| chr4:2721312
|
CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0002g0026others(3): Show | 6 | HG00099.hp1 HG02257.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.4454+5229_4454+523 others(13): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2721312 | |||||
| chr4:2721312
|
CAAAAAAA others(3): Show |
C | 101 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(98): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.4454+5228_4454+523 others(14): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2721312 | |||||
| chr4:2721312
|
CAAAAAAA others(4): Show |
C | 19 | a0001c0001t0002g0017a0001c0001t0002g0022a0001c0001t0002g0091others(16): Show | 19 | HG00408.hp1 HG01074.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.4454+5227_4454+523 others(15): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2721312 | |||||
| chr4:2721357
|
A | G | 78 | a0001c0001t0001g0122a0001c0001t0001g0241a0001c0001t0001g0243others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.4454+5253A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2721357 | ||||||
| chr4:2721450
|
C | A | 1 | a0013c0019t0002g0055 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4454+5346C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2721450 | ||||||
| chr4:2721465
|
G | A | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.4454+5361G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2721465 | ||||||
| chr4:2721522
|
A | C | 246 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.4454+5418A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2721522 | ||||||
| chr4:2721539
|
C | A | 9 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(6): Show | 9 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.4454+5435C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2721539 | ||||||
| chr4:2721580
|
C | A | 1 | a0001c0001t0002g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4454+5476C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2721580 | ||||||
| chr4:2721693
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.4454+5589G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2721693 | ||||||
| chr4:2721711
|
A | G | 5 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(2): Show | 5 | HG01891.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4454+5607A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2721711 | ||||||
| chr4:2721762
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4454+5658C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2721762 | ||||||
| chr4:2721804
|
T | C | 126 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.4454+5700T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2721804 | ||||||
| chr4:2721997
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4454+5893T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2721997 | ||||||
| chr4:2722142
|
G | T | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.4454+6038G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2722142 | ||||||
| chr4:2722237
|
C | T | 5 | a0002c0012t0004g0328a0005c0005t0004g0128a0005c0005t0004g0135others(2): Show | 5 | HG01074.hp1 HG03654.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.4454+6133C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2722237 | ||||||
| chr4:2722577
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4454+6473A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2722577 | ||||||
| chr4:2722657
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.4454+6553G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2722657 | ||||||
| chr4:2722762
|
C | A | 15 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(12): Show | 15 | HG01891.hp2 HG01975.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.4454+6658C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2722762 | ||||||
| chr4:2722831
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4454+6727A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2722831 | ||||||
| chr4:2722932
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4454+6828C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2722932 | ||||||
| chr4:2723145
|
G | A | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4454+7041G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2723145 | ||||||
| chr4:2723346
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4454+7242C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2723346 | ||||||
| chr4:2723573
|
C | CA | 118 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.4454+7482dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2723573 | |||||
| chr4:2723573
|
CA | C | 9 | a0002c0012t0004g0328a0005c0005t0004g0128a0005c0005t0004g0130others(6): Show | 9 | HG00408.hp1 HG01074.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.4454+7482delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2723573 | |||||
| chr4:2723699
|
A | G | 1 | a0001c0002t0009g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4454+7595A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2723699 | ||||||
| chr4:2723768
|
C | T | 4 | a0001c0001t0002g0017a0001c0001t0002g0032a0001c0001t0002g0033others(1): Show | 4 | HG00558.hp2 HG01074.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.4454+7664C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2723768 | ||||||
| chr4:2723791
|
C | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4454+7687C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2723791 | ||||||
| chr4:2723795
|
GTTTT | G | 77 | a0001c0001t0001g0122a0001c0001t0001g0241a0001c0001t0001g0243others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.4454+7694_4454+769 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2723795 | |||||
| chr4:2723861
|
G | C | 22 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(19): Show | 22 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.4454+7757G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2723861 | ||||||
| chr4:2723871
|
G | A | 6 | a0001c0001t0001g0293a0003c0003t0001g0233a0003c0003t0001g0234others(3): Show | 6 | HG01891.hp2 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.4454+7767G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2723871 | ||||||
| chr4:2724029
|
CT | C | 212 | a0001c0001t0001g0065a0001c0001t0001g0122a0001c0001t0001g0133others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.4455-7732delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2724029 | |||||
| chr4:2724029
|
CTT | C | 32 | a0001c0001t0001g0262a0001c0002t0001g0001a0001c0002t0001g0002others(29): Show | 32 | HG00609.hp2 HG01243.hp2 HG01516.hp1 others(29): Show |
intron_variant | MODIFIER | c.4455-7733_4455-773 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2724029 | |||||
| chr4:2724163
|
C | A | 4 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(1): Show | 4 | HG01891.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4455-7612C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2724163 | ||||||
| chr4:2724187
|
C | T | 3 | a0001c0002t0003g0112a0001c0002t0003g0120a0001c0002t0013g0117 | 3 | HG01516.hp1 HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.4455-7588C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2724187 | ||||||
| chr4:2724309
|
TAA | T | 11 | a0001c0021t0003g0143a0004c0004t0001g0318a0004c0004t0001g0321others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4455-7465_4455-746 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2724309 | ||||||
| chr4:2724360
|
G | A | 1 | a0004c0004t0003g0317 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4455-7415G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2724360 | ||||||
| chr4:2724669
|
C | T | 20 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(17): Show | 20 | HG00609.hp2 HG02145.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.4455-7106C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2724669 | ||||||
| chr4:2724818
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4455-6957C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2724818 | ||||||
| chr4:2724862
|
G | A | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.4455-6913G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2724862 | ||||||
| chr4:2724955
|
CAACCTCC others(12): Show |
C | 1 | a0001c0001t0001g0206 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.4455-6819_4455-680 others(23): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2724955 | ||||||
| chr4:2725200
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.4455-6575A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2725200 | ||||||
| chr4:2725216
|
A | G | 16 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.4455-6559A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2725216 | ||||||
| chr4:2725297
|
C | T | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0329 | 3 | HG01106.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4455-6478C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2725297 | ||||||
| chr4:2725360
|
G | C | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4455-6415G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2725360 | ||||||
| chr4:2725404
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4455-6371C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2725404 | ||||||
| chr4:2725450
|
C | CA | 36 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0174others(33): Show | 36 | HG00673.hp1 HG00735.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.4455-6299dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2725450 | |||||
| chr4:2725450
|
C | CAA | 29 | a0001c0001t0001g0152a0001c0002t0001g0001a0001c0002t0001g0002others(26): Show | 29 | HG01243.hp2 HG01516.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.4455-6300_4455-629 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2725450 | |||||
| chr4:2725450
|
CA | C | 7 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0293others(4): Show | 7 | HG01167.hp2 HG03490.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.4455-6299delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2725450 | |||||
| chr4:2725450
|
CAA | C | 17 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(14): Show | 17 | HG00609.hp2 HG02145.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.4455-6300_4455-629 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2725450 | |||||
| chr4:2725512
|
G | A | 20 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(17): Show | 20 | HG00609.hp2 HG02145.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.4455-6263G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2725512 | ||||||
| chr4:2725545
|
G | A | 2 | a0001c0001t0001g0263a0001c0001t0001g0290 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4455-6230G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2725545 | ||||||
| chr4:2725565
|
TGTATAG | T | 5 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(2): Show | 5 | HG01891.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4455-6209_4455-620 others(10): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2725565 | ||||||
| chr4:2725583
|
A | C | 1 | a0001c0001t0006g0016 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.4455-6192A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2725583 | ||||||
| chr4:2725583
|
A | G | 16 | a0003c0003t0001g0233a0003c0003t0001g0234a0003c0003t0001g0235others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.4455-6192A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2725583 | ||||||
| chr4:2725667
|
A | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4455-6108A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2725667 | ||||||
| chr4:2725713
|
CT | C | 8 | a0001c0001t0001g0213a0001c0001t0001g0232a0001c0001t0002g0021others(5): Show | 8 | HG01106.hp1 HG02257.hp1 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.4455-6047delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2725713 | |||||
| chr4:2725760
|
G | A | 3 | a0005c0005t0004g0130a0005c0005t0004g0136a0005c0005t0007g0131 | 3 | HG01975.hp2 HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.4455-6015G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2725760 | ||||||
| chr4:2725936
|
G | T | 22 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(19): Show | 22 | HG00609.hp2 HG02145.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.4455-5839G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2725936 | ||||||
| chr4:2725959
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4455-5816C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2725959 | ||||||
| chr4:2725992
|
A | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0172 | 2 | NA18964.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.4455-5783A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2725992 | ||||||
| chr4:2726052
|
C | A | 1 | a0001c0001t0002g0064 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4455-5723C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2726052 | ||||||
| chr4:2726058
|
C | G | 1 | a0005c0005t0004g0141 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.4455-5717C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2726058 | ||||||
| chr4:2726293
|
G | C | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4455-5482G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2726293 | ||||||
| chr4:2726303
|
C | T | 8 | a0001c0001t0001g0277a0001c0001t0001g0281a0002c0012t0004g0328others(5): Show | 8 | HG00408.hp1 HG01074.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.4455-5472C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2726303 | ||||||
| chr4:2726365
|
C | G | 99 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.4455-5410C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2726365 | ||||||
| chr4:2726416
|
C | T | 1 | a0008c0009t0001g0295 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.4455-5359C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2726416 | ||||||
| chr4:2726459
|
A | G | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.4455-5316A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2726459 | ||||||
| chr4:2726481
|
T | G | 1 | a0001c0001t0001g0305 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4455-5294T>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2726481 | ||||||
| chr4:2726562
|
G | T | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4455-5213G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2726562 | ||||||
| chr4:2726597
|
C | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4455-5178C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2726597 | ||||||
| chr4:2726682
|
A | G | 1 | a0001c0002t0009g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4455-5093A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2726682 | ||||||
| chr4:2726774
|
A | G | 6 | a0004c0004t0001g0318a0004c0004t0001g0321a0004c0004t0001g0322others(3): Show | 6 | HG02258.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.4455-5001A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2726774 | ||||||
| chr4:2726778
|
C | CA | 47 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0151others(44): Show | 47 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.4455-4972dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2726778 | |||||
| chr4:2726778
|
CA | C | 13 | a0001c0001t0001g0165a0001c0001t0001g0283a0001c0001t0002g0009others(10): Show | 13 | HG01243.hp2 HG01257.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.4455-4972delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2726778 | |||||
| chr4:2726778
|
CAA | C | 21 | a0001c0002t0001g0113a0001c0002t0003g0112a0001c0002t0003g0116others(18): Show | 21 | HG01516.hp1 HG02145.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.4455-4973_4455-497 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2726778 | |||||
| chr4:2726778
|
CAAAA | C | 6 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0179others(3): Show | 6 | HG01256.hp2 HG01258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.4455-4975_4455-497 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2726778 | |||||
| chr4:2726807
|
G | A | 2 | a0001c0001t0007g0129a0001c0001t0007g0137 | 2 | HG01167.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4455-4968G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2726807 | ||||||
| chr4:2726869
|
G | A | 2 | a0004c0004t0001g0325a0004c0004t0001g0326 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4455-4906G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2726869 | ||||||
| chr4:2726875
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.4455-4900A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2726875 | ||||||
| chr4:2726950
|
C | CA | 103 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0174others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.4455-4805dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2726950 | |||||
| chr4:2726950
|
C | CAA | 8 | a0001c0001t0001g0152a0001c0001t0002g0020a0001c0001t0002g0021others(5): Show | 8 | HG00673.hp2 HG01106.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.4455-4806_4455-480 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2726950 | |||||
| chr4:2726950
|
CA | C | 38 | a0001c0001t0001g0283a0001c0001t0001g0290a0001c0002t0001g0001others(35): Show | 38 | HG01243.hp2 HG01516.hp1 HG01516.hp2 others(35): Show |
intron_variant | MODIFIER | c.4455-4805delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2726950 | |||||
| chr4:2726950
|
CAAAAAAA | C | 20 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(17): Show | 20 | HG00609.hp2 HG02145.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.4455-4811_4455-480 others(11): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2726950 | |||||
| chr4:2726951
|
A | C | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | HG02015.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.4455-4824A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2726951 | ||||||
| chr4:2727045
|
G | C | 1 | a0014c0024t0018g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4455-4730G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2727045 | ||||||
| chr4:2727077
|
G | A | 6 | a0002c0012t0004g0328a0005c0005t0004g0128a0005c0005t0004g0134others(3): Show | 6 | HG00408.hp1 HG01074.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.4455-4698G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2727077 | ||||||
| chr4:2727120
|
G | A | 1 | a0001c0001t0012g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4455-4655G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2727120 | ||||||
| chr4:2727225
|
C | T | 1 | a0013c0019t0002g0055 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4455-4550C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2727225 | ||||||
| chr4:2727255
|
C | CA | 10 | a0001c0001t0002g0027a0001c0001t0002g0039a0006c0008t0001g0005others(7): Show | 10 | HG00609.hp2 HG00741.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4455-4507dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2727255 | |||||
| chr4:2727308
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4455-4467G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2727308 | ||||||
| chr4:2727385
|
TCTTA | T | 4 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0085others(1): Show | 4 | HG00323.hp2 HG01099.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.4455-4381_4455-437 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2727385 | |||||
| chr4:2727431
|
C | G | 99 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.4455-4344C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2727431 | ||||||
| chr4:2727836
|
C | T | 1 | a0001c0001t0012g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4455-3939C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2727836 | ||||||
| chr4:2727927
|
T | TA | 7 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.4455-3835dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2727927 | |||||
| chr4:2727928
|
A | T | 1 | a0001c0002t0003g0112 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4455-3847A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2727928 | ||||||
| chr4:2727953
|
T | A | 1 | a0001c0001t0001g0167 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4455-3822T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2727953 | ||||||
| chr4:2727956
|
T | A | 21 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(18): Show | 21 | HG00609.hp2 HG02145.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.4455-3819T>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2727956 | ||||||
| chr4:2728045
|
C | T | 21 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(18): Show | 21 | HG00609.hp2 HG02145.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.4455-3730C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2728045 | ||||||
| chr4:2728164
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.4455-3611C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2728164 | ||||||
| chr4:2728215
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.4455-3560C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2728215 | ||||||
| chr4:2728231
|
C | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4455-3544C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2728231 | ||||||
| chr4:2728238
|
A | AT | 180 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0147others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.4455-3512dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2728238 | |||||
| chr4:2728238
|
A | ATT | 42 | a0001c0001t0001g0122a0001c0001t0001g0244a0001c0001t0001g0245others(39): Show | 42 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.4455-3513_4455-351 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2728238 | |||||
| chr4:2728238
|
A | T | 1 | a0001c0001t0001g0206 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.4455-3537A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2728238 | ||||||
| chr4:2728238
|
AT | A | 16 | a0001c0001t0001g0142a0001c0001t0001g0177a0001c0001t0008g0215others(13): Show | 16 | HG00609.hp2 HG02486.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.4455-3512delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2728238 | |||||
| chr4:2728587
|
G | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4455-3188G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2728587 | ||||||
| chr4:2728683
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4455-3092C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2728683 | ||||||
| chr4:2728760
|
T | C | 2 | a0001c0001t0001g0304a0001c0001t0002g0027 | 2 | HG00741.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4455-3015T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2728760 | ||||||
| chr4:2728862
|
A | T | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4455-2913A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2728862 | ||||||
| chr4:2728887
|
C | T | 21 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(18): Show | 21 | HG00609.hp2 HG02145.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.4455-2888C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2728887 | ||||||
| chr4:2728895
|
A | AT | 80 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0008others(77): Show | 80 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.4455-2880_4455-287 others(5): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2728895 | ||||||
| chr4:2728895
|
A | ATT | 12 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0012others(9): Show | 12 | HG00438.hp2 HG01106.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.4455-2880_4455-287 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2728895 | ||||||
| chr4:2728896
|
C | CT | 52 | a0001c0001t0001g0144a0001c0001t0001g0150a0001c0001t0001g0152others(49): Show | 52 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.4455-2853dupT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2728896 | |||||
| chr4:2728896
|
C | CTT | 12 | a0001c0001t0001g0123a0001c0001t0001g0142a0001c0001t0001g0151others(9): Show | 12 | HG01243.hp2 HG01358.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.4455-2854_4455-285 others(6): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2728896 | |||||
| chr4:2728896
|
C | CTTT | 17 | a0001c0002t0001g0113a0001c0002t0003g0112a0001c0002t0003g0116others(14): Show | 17 | HG01516.hp1 HG01891.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.4455-2855_4455-285 others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2728896 | |||||
| chr4:2728896
|
C | CTTTT | 6 | a0001c0001t0008g0215a0004c0004t0001g0325a0004c0004t0001g0327others(3): Show | 6 | HG02622.hp2 HG02723.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.4455-2856_4455-285 others(8): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2728896 | |||||
| chr4:2728896
|
C | CTTTTTTT others(3): Show |
2 | a0006c0008t0001g0121a0006c0008t0001g0125 | 2 | HG02559.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.4455-2862_4455-285 others(14): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2728896 | |||||
| chr4:2728896
|
C | T | 99 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.4455-2879C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2728896 | ||||||
| chr4:2728896
|
CT | C | 7 | a0001c0001t0001g0244a0001c0001t0001g0271a0001c0001t0001g0273others(4): Show | 7 | HG00323.hp1 HG01070.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.4455-2853delT | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2728896 | |||||
| chr4:2728973
|
G | A | 21 | a0001c0001t0008g0215a0001c0021t0003g0143a0004c0004t0001g0318others(18): Show | 21 | HG00609.hp2 HG02145.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.4455-2802G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2728973 | ||||||
| chr4:2728983
|
T | C | 168 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0001g0152others(165): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.4455-2792T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2728983 | ||||||
| chr4:2729290
|
GCGCATGC others(16): Show |
G | 1 | a0001c0001t0002g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4455-2474_4455-245 others(27): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2729290 | |||||
| chr4:2729314
|
C | T | 1 | a0001c0001t0002g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4455-2461C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2729314 | ||||||
| chr4:2729382
|
G | C | 101 | a0001c0001t0001g0065a0001c0001t0002g0006a0001c0001t0002g0007others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.4455-2393G>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2729382 | ||||||
| chr4:2729393
|
G | A | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4455-2382G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2729393 | ||||||
| chr4:2729408
|
A | G | 1 | a0001c0001t0002g0064 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4455-2367A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2729408 | ||||||
| chr4:2729528
|
G | A | 4 | a0004c0004t0001g0321a0004c0004t0003g0317a0004c0004t0003g0319others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.4455-2247G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2729528 | ||||||
| chr4:2729715
|
A | G | 1 | a0001c0001t0001g0244 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4455-2060A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2729715 | ||||||
| chr4:2730017
|
A | C | 1 | a0001c0001t0001g0206 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.4455-1758A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2730017 | ||||||
| chr4:2730213
|
TCTC | T | 21 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(18): Show | 21 | HG01243.hp2 HG01516.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.4455-1558_4455-155 others(7): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2730213 | |||||
| chr4:2730269
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4455-1506A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2730269 | ||||||
| chr4:2730282
|
A | G | 2 | a0004c0004t0001g0323a0004c0004t0001g0327 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4455-1493A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2730282 | ||||||
| chr4:2730346
|
T | C | 4 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(1): Show | 4 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(1): Show |
intron_variant | MODIFIER | c.4455-1429T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2730346 | ||||||
| chr4:2730412
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.4455-1363C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2730412 | ||||||
| chr4:2730428
|
C | G | 1 | a0001c0001t0001g0206 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.4455-1347C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2730428 | ||||||
| chr4:2730430
|
A | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4455-1345A>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2730430 | ||||||
| chr4:2730676
|
C | G | 2 | a0009c0010t0014g0228a0009c0010t0015g0229 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4455-1099C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2730676 | ||||||
| chr4:2730830
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4455-945T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2730830 | ||||||
| chr4:2730832
|
G | A | 108 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.4455-943G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2730832 | ||||||
| chr4:2730963
|
G | A | 121 | a0001c0001t0001g0122a0001c0001t0001g0241a0001c0001t0001g0243others(118): Show | 121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.4455-812G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2730963 | ||||||
| chr4:2730971
|
C | T | 1 | a0001c0001t0008g0215 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4455-804C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2730971 | ||||||
| chr4:2730972
|
G | A | 8 | a0006c0008t0001g0005a0006c0008t0001g0121a0006c0008t0001g0124others(5): Show | 8 | HG00609.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.4455-803G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2730972 | ||||||
| chr4:2731163
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4455-612T>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2731163 | ||||||
| chr4:2731196
|
C | CA | 73 | a0001c0001t0001g0142a0001c0001t0001g0146a0001c0001t0001g0152others(70): Show | 73 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.4455-551dupA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2731196 | |||||
| chr4:2731196
|
C | CAA | 30 | a0001c0001t0001g0151a0001c0001t0001g0172a0001c0001t0001g0178others(27): Show | 30 | HG00544.hp2 HG00735.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.4455-552_4455-551d others(4): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2731196 | |||||
| chr4:2731196
|
CA | C | 30 | a0001c0001t0001g0231a0001c0002t0001g0001a0001c0002t0001g0002others(27): Show | 30 | HG00408.hp1 HG01243.hp2 HG01516.hp1 others(27): Show |
intron_variant | MODIFIER | c.4455-551delA | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2731196 | |||||
| chr4:2731196
|
CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0002g0025a0001c0001t0002g0045a0001c0001t0002g0063others(2): Show | 5 | HG00735.hp1 HG02056.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.4455-562_4455-551d others(14): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2731196 | |||||
| chr4:2731196
|
CAAAAAAA others(6): Show |
C | 103 | a0001c0001t0001g0065a0001c0001t0001g0133a0001c0001t0002g0006others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.4455-563_4455-551d others(15): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2731196 | |||||
| chr4:2731196
|
CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0001g0150a0001c0001t0010g0149 | 2 | HG00639.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.4455-566_4455-551d others(18): Show |
FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr4 | 2731196 | |||||
| chr4:2731208
|
A | C | 1 | a0001c0001t0001g0123 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.4455-567A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2731208 | ||||||
| chr4:2731215
|
A | C | 1 | a0001c0001t0001g0169 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.4455-560A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2731215 | ||||||
| chr4:2731219
|
A | C | 1 | a0008c0009t0001g0310 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.4455-556A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2731219 | ||||||
| chr4:2731225
|
C | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0296 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4455-550C>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2731225 | ||||||
| chr4:2731264
|
G | T | 1 | a0001c0002t0003g0112 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4455-511G>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2731264 | ||||||
| chr4:2731265
|
A | C | 1 | a0001c0002t0003g0112 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4455-510A>C | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2731265 | ||||||
| chr4:2731372
|
A | T | 1 | a0001c0001t0002g0050 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.4455-403A>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2731372 | ||||||
| chr4:2731393
|
C | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG00639.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.4455-382C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2731393 | ||||||
| chr4:2731506
|
C | G | 22 | a0001c0001t0001g0157a0001c0001t0001g0168a0001c0001t0001g0170others(19): Show | 22 | HG01167.hp2 HG01891.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.4455-269C>G | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2731506 | ||||||
| chr4:2731506
|
C | T | 2 | a0001c0001t0001g0302a0001c0002t0003g0119 | 2 | HG02970.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.4455-269C>T | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2731506 | ||||||
| chr4:2731727
|
G | A | 7 | a0001c0001t0002g0036a0001c0001t0002g0038a0001c0001t0002g0066others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.4455-48G>A | FAM193A | ENSG00000125386.16 | transcript | ENST00000637812.2 | protein_coding | 20/20 | chr4 | 2731727 |